BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Nakamura Y, Leppert M, O'connell P, Wolff R, Holm T, Culver M, Martin C, Fujimoto E, Hoff M, Kumlin E, et A. Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 1987;235:1616-22. [DOI: 10.1126/science.3029872] [Cited by in Crossref: 1055] [Cited by in F6Publishing: 735] [Article Influence: 31.0] [Reference Citation Analysis]
Number Citing Articles
1 Wasmuth JJ, Hewitt J, Smith B, Allard D, Haines JL, Skarecky D, Partlow E, Hayden MR. A highly polymorphic locus very tightly linked to the Huntington's disease gene. Nature 1988;332:734-6. [PMID: 2895895 DOI: 10.1038/332734a0] [Cited by in Crossref: 97] [Cited by in F6Publishing: 78] [Article Influence: 2.9] [Reference Citation Analysis]
2 Vijay A, Garg I, Ashraf MZ. Perspective: DNA Copy Number Variations in Cardiovascular Diseases. Epigenet Insights 2018;11:2516865718818839. [PMID: 30560231 DOI: 10.1177/2516865718818839] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
3 Davis CL, Field D, Metzgar D, Saiz R, Morin PA, Smith IL, Spector SA, Wills C. Numerous length polymorphisms at short tandem repeats in human cytomegalovirus. J Virol 1999;73:6265-70. [PMID: 10400717 DOI: 10.1128/JVI.73.8.6265-6270.1999] [Cited by in Crossref: 35] [Cited by in F6Publishing: 12] [Article Influence: 1.6] [Reference Citation Analysis]
4 Koperdáková J, Kosuth J, Cellárová E. Variation in the content of hypericins in four generations of seed progeny of Hypericum perforatum somaclones. J Plant Res 2007;120:123-8. [PMID: 17072497 DOI: 10.1007/s10265-006-0031-6] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
5 Bhattacharya E, Ranade SA. Molecular distinction amongst varieties of mulberry using RAPD and DAMD profiles. BMC Plant Biol 2001;1:3. [PMID: 11801190 DOI: 10.1186/1471-2229-1-3] [Cited by in Crossref: 32] [Cited by in F6Publishing: 17] [Article Influence: 1.6] [Reference Citation Analysis]
6 Leon SP, Zhu J, Black PM. Genetic Aberrations in Human Brain Tumors. Neurosurgery 1994;34:708-22. [DOI: 10.1097/00006123-199404000-00021] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
7 Lee SD, Shin CH, Kim KB, Lee YS, Lee JB. Sequence variation of mitochondrial DNA control region in Koreans. Forensic Sci Int 1997;87:99-116. [PMID: 9237373 DOI: 10.1016/s0379-0738(97)02114-2] [Cited by in Crossref: 46] [Cited by in F6Publishing: 11] [Article Influence: 1.9] [Reference Citation Analysis]
8 Corach D, Sala A, Penacino G, Sotelo A. Mass disasters: Rapid molecular screening of human remains by means of short tandem repeats typing. Electrophoresis 1995;16:1617-23. [DOI: 10.1002/elps.11501601267] [Cited by in Crossref: 33] [Cited by in F6Publishing: 11] [Article Influence: 1.3] [Reference Citation Analysis]
9 Trepicchio WL, Krontiris TG. Members of the rel/NF-kappa B family of transcriptional regulatory proteins bind the HRAS1 minisatellite DNA sequence. Nucleic Acids Res 1992;20:2427-34. [PMID: 1598201 DOI: 10.1093/nar/20.10.2427] [Cited by in Crossref: 50] [Cited by in F6Publishing: 46] [Article Influence: 1.7] [Reference Citation Analysis]
10 Dawson DB, Cummins LA, Schaid DJ, Michels VV, Gordon H, O'connell EJ, Thibodeau SN. Carrier Identification of Cystic Fibrosis by Recombinant DNA Techniques. Mayo Clinic Proceedings 1989;64:325-34. [DOI: 10.1016/s0025-6196(12)65252-5] [Cited by in Crossref: 2] [Article Influence: 0.1] [Reference Citation Analysis]
11 Zückert WR, Barbour AG. Stability of Borrelia burgdorferi bdr loci in vitro and in vivo. Infect Immun 2000;68:1727-30. [PMID: 10678998 DOI: 10.1128/IAI.68.3.1727-1730.2000] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
12 St Lezin EM, Pravenec M, Wong AL, Liu W, Wang N, Lu S, Jacob HJ, Roman RJ, Stec DE, Wang JM, Reid IA, Kurtz TW. Effects of renin gene transfer on blood pressure and renin gene expression in a congenic strain of Dahl salt-resistant rats. J Clin Invest 1996;97:522-7. [PMID: 8567976 DOI: 10.1172/JCI118444] [Cited by in Crossref: 39] [Cited by in F6Publishing: 7] [Article Influence: 1.6] [Reference Citation Analysis]
13 Fries R, Eggen A, Stranzinger G. The bovine genome contains polymorphic microsatellites. Genomics 1990;8:403-6. [DOI: 10.1016/0888-7543(90)90301-a] [Cited by in Crossref: 52] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]
14 Romani M, De Ambrosis A, Alhadeff B, Purrello M, Gluzman Y, Siniscalco M. Preferential integration of the Ad5/SV40 hybrid virus at the highly recombinogenic human chromosomal site 1p36. Gene 1990;95:231-41. [PMID: 2174396 DOI: 10.1016/0378-1119(90)90366-y] [Cited by in Crossref: 14] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
15 Kashi Y, Nave A, Darvasi A, Gruenbaum Y, Soller M, Beckmann JS. How is it that microsatellites and random oligonucleotides uncover DNA fingerprint patterns? Mammalian Genome 1994;5:525-30. [DOI: 10.1007/bf00354924] [Cited by in Crossref: 2] [Article Influence: 0.1] [Reference Citation Analysis]
16 Smeets HJM, Brunner HG, Ropers H, Wieringa B. Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy. Hum Genet 1989;83:245-51. [DOI: 10.1007/bf00285165] [Cited by in Crossref: 50] [Cited by in F6Publishing: 6] [Article Influence: 1.6] [Reference Citation Analysis]
17 Henke J, Henke L. Recent observations in human DNA-minisatellite mutations. Int J Legal Med 1995;107:204-8. [PMID: 7599098 DOI: 10.1007/BF01428407] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
18 Yashiro M, Chung YS, Nishimura S, Inoue T, Sowa M. Establishment of two new scirrhous gastric cancer cell lines: analysis of factors associated with disseminated metastasis. Br J Cancer 1995;72:1200-10. [PMID: 7577468 DOI: 10.1038/bjc.1995.486] [Cited by in Crossref: 57] [Cited by in F6Publishing: 56] [Article Influence: 2.2] [Reference Citation Analysis]
19 Rogstad SH, Patton JC 2nd, Schaal BA. M13 repeat probe detects DNA minisatellite-like sequences in gymnosperms and angiosperms. Proc Natl Acad Sci U S A 1988;85:9176-8. [PMID: 3194419 DOI: 10.1073/pnas.85.23.9176] [Cited by in Crossref: 90] [Cited by in F6Publishing: 41] [Article Influence: 2.7] [Reference Citation Analysis]
20 Hillel J, Plotzy Y, Haberfeld A, Lavi U, Cahaner A, Jeffreys AJ. DNA fingerprints of poultry. Animal Genetics 1989;20:145-55. [DOI: 10.1111/j.1365-2052.1989.tb00852.x] [Cited by in Crossref: 47] [Cited by in F6Publishing: 22] [Article Influence: 3.9] [Reference Citation Analysis]
21 Lamont SJ, Lakshmanan N, Plotsky Y, Kaiser MG, Kuhn M, Arthur JA, Beck NJ, O'sullivan NP. Genetic markers linked to quantitative traits in poultry. Animal Genetics 1996;27:1-8. [DOI: 10.1111/j.1365-2052.1996.tb01170.x] [Cited by in Crossref: 20] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
22 Satoh C, Takahashi N, Asakawa J, Kodaira M, Kuick R, Hanash SM, Neel JV. Genetic analysis of children of atomic bomb survivors. Environ Health Perspect 1996;104 Suppl 3:511-9. [PMID: 8781374 DOI: 10.1289/ehp.96104s3511] [Cited by in Crossref: 31] [Cited by in F6Publishing: 21] [Article Influence: 1.3] [Reference Citation Analysis]
23 Salem A, Myers JS, Otieno AC, Scott Watkins W, Jorde LB, Batzer MA. LINE-1 preTa Elements in the Human Genome. Journal of Molecular Biology 2003;326:1127-46. [DOI: 10.1016/s0022-2836(03)00032-9] [Cited by in Crossref: 23] [Cited by in F6Publishing: 16] [Article Influence: 1.3] [Reference Citation Analysis]
24 Krawczak M, Böhm I, Nürnberg P, Hampe J, Hundrieser J, Pöche H, Peters C, Slomski R, Kwiatkowska J, Nagy M. Paternity testing with oligonucleotide multilocus probe (CAC)5/(GTG)5: a multicenter study. Forensic Sci Int 1993;59:101-17. [PMID: 8330804 DOI: 10.1016/0379-0738(93)90149-5] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
25 Gottlieb J, Muzyczka N. In vitro excision of adeno-associated virus DNA from recombinant plasmids: isolation of an enzyme fraction from HeLa cells that cleaves DNA at poly(G) sequences. Mol Cell Biol 1988;8:2513-22. [PMID: 2841582 DOI: 10.1128/mcb.8.6.2513-2522.1988] [Cited by in Crossref: 25] [Article Influence: 0.8] [Reference Citation Analysis]
26 van Belkum A, De Jonckheere J, Quint WG. Genotyping Naegleria spp. and Naegleria fowleri isolates by interrepeat polymerase chain reaction. J Clin Microbiol 1992;30:2595-8. [DOI: 10.1128/jcm.30.10.2595-2598.1992] [Cited by in Crossref: 29] [Cited by in F6Publishing: 11] [Article Influence: 1.0] [Reference Citation Analysis]
27 Fuentes J, Banchs I, Volpini V, Estivill X. Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish population. Int J Leg Med 1993;105:271-7. [DOI: 10.1007/bf01370384] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
28 Wolff R, Nakamura Y, Odelberg S, Shiang R, White R. Generation of Variability at VNTR Loci in Human DNA. In: Burke T, Dolf G, Jeffreys AJ, Wolff R, editors. DNA Fingerprinting: Approaches and Applications. Basel: Birkhäuser; 1991. pp. 20-38. [DOI: 10.1007/978-3-0348-7312-3_2] [Cited by in Crossref: 13] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
29 Schaffer FM, Palermos J, Zhu ZB, Barger BO, Cooper MD, Volanakis JE. Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes. Proc Natl Acad Sci U S A 1989;86:8015-9. [PMID: 2573059 DOI: 10.1073/pnas.86.20.8015] [Cited by in Crossref: 112] [Cited by in F6Publishing: 98] [Article Influence: 3.5] [Reference Citation Analysis]
30 Singh S, Simon M, Meybohm I, Jantke I, Jonat W, Maass H, Goedde HW. Human breast cancer: frequent p53 allele loss and protein overexpression. Hum Genet 1993;90:635-40. [PMID: 8444469 DOI: 10.1007/BF00202481] [Cited by in Crossref: 23] [Cited by in F6Publishing: 11] [Article Influence: 0.8] [Reference Citation Analysis]
31 Mosges G, Friedtu W. Genetic 'Fingerprinting' of Sunflower Lines and F1 Hybrids using. Isozymes, Simple and Repetitive Sequences as Hybridization Probes, and Random Primers for PCR. Plant Breeding 1994;113:114-24. [DOI: 10.1111/j.1439-0523.1994.tb00713.x] [Cited by in Crossref: 17] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
32 Nishimaki Y, Sato K, Fang L, Ma M, Hasekura H, Boettcher B. Sequence polymorphism in the mtDNA HV1 region in Japanese and Chinese. Legal Medicine 1999;1:238-49. [DOI: 10.1016/s1344-6223(99)80044-3] [Cited by in Crossref: 31] [Cited by in F6Publishing: 8] [Article Influence: 1.4] [Reference Citation Analysis]
33 Zumwalt RE. Application of molecular biology to forensic pathology. Human Pathology 1989;20:303-7. [DOI: 10.1016/0046-8177(89)90037-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
34 Deka R, De Croo S, Yu LM, Ferrell RE. Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations. Hum Genet 1992;90:86-90. [PMID: 1427793 DOI: 10.1007/BF00210749] [Cited by in Crossref: 19] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
35 Sasaki M, Shiono H, Fukushima T, Shimizu K. Human identification by genotyping of personal articles. Forensic Science International 1997;90:65-75. [DOI: 10.1016/s0379-0738(97)00150-3] [Cited by in Crossref: 7] [Article Influence: 0.3] [Reference Citation Analysis]
36 Weber JL. Human DNA polymorphisms and methods of analysis. Curr Opin Biotechnol 1990;1:166-71. [PMID: 1367853 DOI: 10.1016/0958-1669(90)90026-h] [Cited by in Crossref: 65] [Cited by in F6Publishing: 21] [Article Influence: 2.2] [Reference Citation Analysis]
37 Hilbert P, Marcotte A, Schwers A, Hanset R, Vassart G, Georges M. Analysis of genetic variation in the Belgian Blue Cattle breed using DNA sequence polymorphism at the growth hormone, low density lipoprotein receptor, α-subunit of glycoprotein hormones and thyroglobulin loci. Animal Genetics 1989;20:383-94. [DOI: 10.1111/j.1365-2052.1989.tb00894.x] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
38 Liu P, Erez A, Nagamani SC, Bi W, Carvalho CM, Simmons AD, Wiszniewska J, Fang P, Eng PA, Cooper ML, Sutton VR, Roeder ER, Bodensteiner JB, Delgado MR, Prakash SK, Belmont JW, Stankiewicz P, Berg JS, Shinawi M, Patel A, Cheung SW, Lupski JR. Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications. Hum Mol Genet 2011;20:1975-88. [PMID: 21355048 DOI: 10.1093/hmg/ddr078] [Cited by in Crossref: 53] [Cited by in F6Publishing: 43] [Article Influence: 5.3] [Reference Citation Analysis]
39 Holgersson S, Karlsson J, Kihlgren A, Rosén B, Savolainen P, Gyllensten U. Fluorescent-based typing of the two short tandem repeat loci HUMTH01 and HUMACTBP2: Reproducibility of size measurements and genetic variation in the swedish population. Electrophoresis 1994;15:890-5. [DOI: 10.1002/elps.11501501127] [Cited by in Crossref: 18] [Cited by in F6Publishing: 10] [Article Influence: 0.7] [Reference Citation Analysis]
40 Jeffreys AJ, Macleod A, Tamaki K, Neil DL, Monckton DG. Minisatellite repeat coding as a digital approach to DNA typing. Nature 1991;354:204-9. [DOI: 10.1038/354204a0] [Cited by in Crossref: 251] [Cited by in F6Publishing: 177] [Article Influence: 8.4] [Reference Citation Analysis]
41 Wells RA, Green P, Reeders ST. Simultaneous genetic mapping of multiple human minisatellite sequences using DNA fingerprinting. Genomics 1989;5:761-72. [PMID: 2574144 DOI: 10.1016/0888-7543(89)90118-3] [Cited by in Crossref: 23] [Cited by in F6Publishing: 22] [Article Influence: 0.7] [Reference Citation Analysis]
42 Pinheiro M, Pontes M, Huguet E, Gené M, da Costa J, Moreno P. Study of three AMPFLPs (D1S80, 3′ApoB and YNZ22) in the population of the North of Portugal. Forensic Science International 1996;79:23-9. [DOI: 10.1016/0379-0738(95)01883-2] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
43 Kennedy B, Verrinder Gibbins A, Gibson J, Smith C. Coalescence of Molecular and Quantitative Genetics for Livestock Improvement. Journal of Dairy Science 1990;73:2619-27. [DOI: 10.3168/jds.s0022-0302(90)78948-5] [Cited by in Crossref: 7] [Article Influence: 0.2] [Reference Citation Analysis]
44 Ramachandra L, Rao MR. Identification and sequence characterization of a 1.3 Kb EcoRI repeat fragment that harbors a DNA repair site of rat pachytene spermatocytes. Chromosoma 1994;103:486-501. [PMID: 7720415 DOI: 10.1007/BF00337387] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
45 Lathrop G, O'connell P, Leppert M, Nakamura Y, Farrall M, Tsui L, Lalouel J, White R. Twenty-five loci form a continuous linkage map of markers for human chromosome 7. Genomics 1989;5:866-73. [DOI: 10.1016/0888-7543(89)90128-6] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 0.8] [Reference Citation Analysis]
46 Ali S, Wallace RB. Intrinsic polymorphism of variable number tandem repeat loci in the human genome. Nucleic Acids Res 1988;16:8487-96. [PMID: 2901724 DOI: 10.1093/nar/16.17.8487] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 0.8] [Reference Citation Analysis]
47 Johnson PH, Cadiou H, Hopkinson DA. Detection of the common alpha-1-antitrypsin variants by denaturing gradient gel electrophoresis. Ann Human Genet 1991;55:183-98. [DOI: 10.1111/j.1469-1809.1991.tb00413.x] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.2] [Reference Citation Analysis]
48 Nybom H, Schaal BA. DNA "fingerprints" applied to paternity analysis in apples (Malus x domestica). Theor Appl Genet 1990;79:763-8. [PMID: 24226736 DOI: 10.1007/BF00224242] [Cited by in Crossref: 63] [Cited by in F6Publishing: 5] [Article Influence: 7.9] [Reference Citation Analysis]
49 Richards B, Horn GT, Merrill JJ, Klinger KW. Characterization and rapid analysis of the highly polymorphic VNTR locus D4S125 (YNZ32), closely linked to the Huntington disease gene. Genomics 1991;9:235-40. [PMID: 1672295 DOI: 10.1016/0888-7543(91)90247-c] [Cited by in Crossref: 12] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
50 Dizon-townson DS, Major H, Varner M, Ward K. A promoter mutation that increases transcription of the tumor necrosis factor-α gene is not associated with preterm delivery. American Journal of Obstetrics and Gynecology 1997;177:810-3. [DOI: 10.1016/s0002-9378(97)70273-4] [Cited by in Crossref: 46] [Cited by in F6Publishing: 10] [Article Influence: 1.9] [Reference Citation Analysis]
51 Gao Q, Yeung ES. A Matrix for DNA Separation:  Genotyping and Sequencing Using Poly(vinylpyrrolidone) Solution in Uncoated Capillaries. Anal Chem 1998;70:1382-8. [DOI: 10.1021/ac970999h] [Cited by in Crossref: 168] [Cited by in F6Publishing: 120] [Article Influence: 7.3] [Reference Citation Analysis]
52 Klevytska AM, Price LB, Schupp JM, Worsham PL, Wong J, Keim P. Identification and characterization of variable-number tandem repeats in the Yersinia pestis genome. J Clin Microbiol 2001;39:3179-85. [PMID: 11526147 DOI: 10.1128/JCM.39.9.3179-3185.2001] [Cited by in Crossref: 159] [Cited by in F6Publishing: 76] [Article Influence: 8.0] [Reference Citation Analysis]
53 van Belkum A, Ramesar J, Trommelen G, Uitterlinden A. Mini- and micro-satellites in the genome of rodent malaria parasites. Gene 1992;118:81-6. [DOI: 10.1016/0378-1119(92)90251-j] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
54 Hyytiä-Trees EK, Cooper K, Ribot EM, Gerner-Smidt P. Recent developments and future prospects in subtyping of foodborne bacterial pathogens. Future Microbiol 2007;2:175-85. [PMID: 17661654 DOI: 10.2217/17460913.2.2.175] [Cited by in Crossref: 57] [Cited by in F6Publishing: 38] [Article Influence: 4.1] [Reference Citation Analysis]
55 Nakamura Y, Fujimoto E, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pEFD64.1) on chromosome 3. Nucleic Acids Res 1988;16:10947. [PMID: 2905043 DOI: 10.1093/nar/16.22.10947] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
56 Mackenzie AE, Macleod HL, Heick HM, Korneluk RG. False positive results from the alanine loading test for ornithine carbamoyltransferase deficiency heterozygosity. The Journal of Pediatrics 1989;115:605-8. [DOI: 10.1016/s0022-3476(89)80294-x] [Cited by in Crossref: 5] [Article Influence: 0.2] [Reference Citation Analysis]
57 Cahill TC, Bookstein R, Axelrod F, Ngo K, Scioscia AL. Resolution of DNA linkage discrepancies through analysis of a VNTR locus in a family study of cystic fibrosis. Prenat Diagn 1990;10:795-9. [DOI: 10.1002/pd.1970101206] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
58 Kandt RS, Pericak-vance MA, Hung W, Gardner RJM, Crossen PE, Nellist MD, Speer MC, Roses AD. Linkage Studies in Tuberous Sclerosis.: Chromosome 9?, 11?, or Maybe 14! Ann NY Acad Sci 1991;615:284-97. [DOI: 10.1111/j.1749-6632.1991.tb37770.x] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 0.3] [Reference Citation Analysis]
59 Kunieda T, Ikadai H, Matsui M, Nomura N, Imamichi T, Ishizaki R. Novel restriction fragment length polymorphism of the growth hormone gene in inbred rats. Biochem Genet 1989;27:591-602. [PMID: 2575899 DOI: 10.1007/BF02396154] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.1] [Reference Citation Analysis]
60 Nakamura Y, Culver M, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pYNZ32) on chromosome 4p [D4S125]. Nucleic Acids Res 1988;16:4186. [PMID: 2897672 DOI: 10.1093/nar/16.9.4186] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 0.5] [Reference Citation Analysis]
61 Pöche H, Peters C, Wrobel G, Schneider V, Epplen JT. Determining consanguinity by oligonucleotide fingerprinting with (GTG)5/(CAC)5. Electrophoresis 1991;12:397-402. [DOI: 10.1002/elps.1150120603] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
62 Mcquinn T. Molecular biological approaches to genetic cardiac diseases. Progress in Pediatric Cardiology 1996;6:1-18. [DOI: 10.1016/1058-9813(96)00167-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
63 Decorte R, Cuppens H, Marynen P, Cassiman J. Rapid Detection of Hypervariable Regions by the Polymerase Chain Reaction Technique. DNA and Cell Biology 1990;9:461-9. [DOI: 10.1089/dna.1990.9.461] [Cited by in Crossref: 54] [Cited by in F6Publishing: 42] [Article Influence: 1.7] [Reference Citation Analysis]
64 Chakraborty R, Jin L. A unified approach to study hypervariable polymorphisms: statistical considerations of determining relatedness and population distances. EXS 1993;67:153-75. [PMID: 8400687 DOI: 10.1007/978-3-0348-8583-6_14] [Cited by in Crossref: 103] [Cited by in F6Publishing: 81] [Article Influence: 3.7] [Reference Citation Analysis]
65 Senthilkumar R, Sabarinathan R, Hameed BS, Banerjee N, Chidambarathanu N, Karthik R, Sekar K. FAIR: A server for internal sequence repeats. Bioinformation 2010;4:271-5. [PMID: 20978598 DOI: 10.6026/97320630004271] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
66 O'hara PJ, Grant FJ. The human factor VII gene is polymorphic due to variation in repeat copy number in a minisatellite. Gene 1988;66:147-58. [DOI: 10.1016/0378-1119(88)90232-6] [Cited by in Crossref: 23] [Cited by in F6Publishing: 15] [Article Influence: 0.7] [Reference Citation Analysis]
67 Mariat D, De Gouyon B, Julier C, Lathrop M, Vergnaud G. Genetic mapping through the use of synthetic tandem repeats in the mouse genome. Mamm Genome 1993;4:135-40. [PMID: 8094987 DOI: 10.1007/BF00352228] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
68 Bamforth F, Machin G, Innes M. X-chromosome inactivation is mostly random in placental tissues of female monozygotic twins and triplets. Am J Med Genet 1996;61:209-15. [DOI: 10.1002/(sici)1096-8628(19960122)61:3<209::aid-ajmg4>3.0.co;2-p] [Cited by in Crossref: 22] [Cited by in F6Publishing: 3] [Article Influence: 0.9] [Reference Citation Analysis]
69 Carlson DM, Zhou J, Wright PS. Molecular Structure and Transcriptional Regulation of the Salivary Gland Proline-Rich Protein Multigene Families. Elsevier; 1991. pp. 1-22. [DOI: 10.1016/s0079-6603(08)60005-7] [Cited by in Crossref: 14] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
70 Thompson AM, Anderson TJ, Condie A, Prosser J, Chetty U, Carter DC, Evans HJ, Steel CM. p53 allele losses, mutations and expression in breast cancer and their relationship to clinico-pathological parameters. Int J Cancer 1992;50:528-32. [DOI: 10.1002/ijc.2910500405] [Cited by in Crossref: 101] [Cited by in F6Publishing: 106] [Article Influence: 3.5] [Reference Citation Analysis]
71 Rico C, Kuhnlein U, Fitzgerald GJ. Male reproductive tactics in the threespine stickleback– an evaluation by DNA fingerprinting. Mol Ecol 1992;1:79-87. [DOI: 10.1111/j.1365-294x.1992.tb00159.x] [Cited by in Crossref: 57] [Article Influence: 2.0] [Reference Citation Analysis]
72 Eng B, Chui DH, Saunderson J, Olivieri NF, Waye JS. Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletion. Hum Mutat 1993;2:375-9. [PMID: 8257991 DOI: 10.1002/humu.1380020509] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 0.4] [Reference Citation Analysis]
73 Law A, Richard CW, Cottingham RW, Lathrop GM, Cox DR, Myers RM. Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree. Hum Genet 1992;88:562-8. [DOI: 10.1007/bf00219345] [Cited by in Crossref: 15] [Article Influence: 0.5] [Reference Citation Analysis]
74 Sankaranarayanan K. Ionizing radiation and genetic risks I. Epidemiological, population genetic, biochemical and molecular aspects of mendelian diseases. Mutation Research/Reviews in Genetic Toxicology 1991;258:3-49. [DOI: 10.1016/0165-1110(91)90027-s] [Cited by in Crossref: 22] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
75 Zhang K, Nguyen TE, Crandall A, Donoso LA. Genetic and molecular studies of macular dystrophies: recent developments. Survey of Ophthalmology 1995;40:51-61. [DOI: 10.1016/s0039-6257(95)80047-6] [Cited by in Crossref: 19] [Article Influence: 0.7] [Reference Citation Analysis]
76 Tefferi A, Wieben ED, Dewald GW, Whiteman DA, Bernard ME, Spelsberg TC. Primer on Medical Genomics Part II: Background Principles and Methods in Molecular Genetics. Mayo Clinic Proceedings 2002;77:785-808. [DOI: 10.4065/77.8.785] [Cited by in Crossref: 24] [Cited by in F6Publishing: 13] [Article Influence: 1.3] [Reference Citation Analysis]
77 Paetkau D, Strobeck C. Microsatellite analysis of genetic variation in black bear populations. Mol Ecol 1994;3:489-95. [DOI: 10.1111/j.1365-294x.1994.tb00127.x] [Cited by in Crossref: 426] [Cited by in F6Publishing: 37] [Article Influence: 15.8] [Reference Citation Analysis]
78 Gupta R, Mirdha BR, Guleria R, Kumar L, Luthra K, Agarwal SK, Sreenivas V. Genetic characterization of UCS region of Pneumocystis jirovecii and construction of allelic profiles of Indian isolates based on sequence typing at three regions. Infection, Genetics and Evolution 2013;13:180-6. [DOI: 10.1016/j.meegid.2012.07.013] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
79 Rogstad SH, Nybom H, Schaal BA. The tetrapod ?DNA fingerprinting? M13 repeat probe reveals genetic diversity and clonal growth in quaking aspen (Populus tremuloides, Salicaceae). Pl Syst Evol 1991;175:115-23. [DOI: 10.1007/bf00937841] [Cited by in Crossref: 35] [Article Influence: 1.2] [Reference Citation Analysis]
80 de Belleroche J, Leigh PN, Clifford Rose F. Familial Motor Neuron Disease. In: Leigh PN, Swash M, editors. Motor Neuron Disease. London: Springer; 1995. pp. 35-51. [DOI: 10.1007/978-1-4471-1871-8_3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
81 Slavin S, Nagler A, Naparstek E, Aker M, Cividalli G, Varadi G, Ackerstein A, Samuel S, Amar A, Brautbar C, Or R. Minitransplants and cell-based therapies for malignant and nonmalignant disorders: . Current Opinion in Organ Transplantation 1999;4:184-8. [DOI: 10.1097/00075200-199909000-00002] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.2] [Reference Citation Analysis]
82 Boylan KB, Merrill Ayres T, Popko B, Takahashi N, Hood LE, Prusiner SB. Repetitive DNA (TGGA)n 5′ to the human myelin basic protein gene: A new form of oligonucleotide repetitive sequence showing length polymorphism. Genomics 1990;6:16-22. [DOI: 10.1016/0888-7543(90)90443-x] [Cited by in Crossref: 31] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
83 Baine I, Hui P. Practical applications of DNA genotyping in diagnostic pathology. Expert Rev Mol Diagn 2019;19:175-88. [PMID: 30638393 DOI: 10.1080/14737159.2019.1568874] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
84 Brewer DA, Bokey EL, Fung C, Chapuls PH. HEREDITY, MOLECULAR GENETICS AND COLORECTAL CANCER: A REVIEW. ANZ J Surg 1993;63:87-94. [DOI: 10.1111/j.1445-2197.1993.tb00051.x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
85 Farag SS, Srivastava S, Messina-Graham S, Schwartz J, Robertson MJ, Abonour R, Cornetta K, Wood L, Secrest A, Strother RM, Jones DR, Broxmeyer HE. In vivo DPP-4 inhibition to enhance engraftment of single-unit cord blood transplants in adults with hematological malignancies. Stem Cells Dev 2013;22:1007-15. [PMID: 23270493 DOI: 10.1089/scd.2012.0636] [Cited by in Crossref: 88] [Cited by in F6Publishing: 68] [Article Influence: 11.0] [Reference Citation Analysis]
86 Konishi M, Kikuchi-Yanoshita R, Tanaka K, Sato C, Tsuruta K, Maeda Y, Koike M, Tanaka S, Nakamura Y, Hattori N. Genetic changes and histopathological grades in human hepatocellular carcinomas. Jpn J Cancer Res 1993;84:893-9. [PMID: 8407553 DOI: 10.1111/j.1349-7006.1993.tb02063.x] [Cited by in Crossref: 39] [Cited by in F6Publishing: 41] [Article Influence: 1.4] [Reference Citation Analysis]
87 Ross PL, Belgrader P. Analysis of Short Tandem Repeat Polymorphisms in Human DNA by Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry. Anal Chem 1997;69:3966-72. [DOI: 10.1021/ac970312t] [Cited by in Crossref: 45] [Cited by in F6Publishing: 39] [Article Influence: 1.9] [Reference Citation Analysis]
88 Iwasaki H, Stewart PW, Dilley WG, Holt MS, Steinbrueck TD, Wells SA, Donis-keller H. A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95. Genomics 1992;13:7-15. [DOI: 10.1016/0888-7543(92)90194-w] [Cited by in Crossref: 31] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
89 Queller DC, Strassmann JE, Hughes CR. Microsatellites and kinship. Trends Ecol Evol 1993;8:285-8. [PMID: 21236170 DOI: 10.1016/0169-5347(93)90256-O] [Cited by in Crossref: 448] [Cited by in F6Publishing: 34] [Article Influence: 49.8] [Reference Citation Analysis]
90 Gatti RA, Berkel I, Boder E, Braedt G, Charmley P, Concannon P, Ersoy F, Foroud T, Jaspers NG, Lange K. Localization of an ataxia-telangiectasia gene to chromosome 11q22-23. Nature. 1988;336:577-580. [PMID: 3200306 DOI: 10.1038/336577a0] [Cited by in Crossref: 463] [Cited by in F6Publishing: 351] [Article Influence: 14.5] [Reference Citation Analysis]
91 Powell JT, Turner RJ, Henney AM, Miller GJ, Humphries SE. An association between arterial pulse pressure and variation in the fibrillin-1 gene. Heart 1997;78:396-8. [PMID: 9404258 DOI: 10.1136/hrt.78.4.396] [Cited by in Crossref: 21] [Cited by in F6Publishing: 14] [Article Influence: 0.9] [Reference Citation Analysis]
92 Wren JD, Forgacs E, Fondon JW 3rd, Pertsemlidis A, Cheng SY, Gallardo T, Williams RS, Shohet RV, Minna JD, Garner HR. Repeat polymorphisms within gene regions: phenotypic and evolutionary implications. Am J Hum Genet 2000;67:345-56. [PMID: 10889045 DOI: 10.1086/303013] [Cited by in Crossref: 92] [Cited by in F6Publishing: 70] [Article Influence: 4.4] [Reference Citation Analysis]
93 Georges M, Lathrop M, Hilbert P, Marcotte A, Schwers A, Swillens S, Vassart G, Hanset R. On the use of DNA fingerprints for linkage studies in cattle. Genomics 1990;6:461-74. [DOI: 10.1016/0888-7543(90)90476-b] [Cited by in Crossref: 64] [Cited by in F6Publishing: 6] [Article Influence: 2.1] [Reference Citation Analysis]
94 Kaneda S, Nalbantoglu J, Takeishi K, Shimizu K, Gotoh O, Seno T, Ayusawa D. Structural and functional analysis of the human thymidylate synthase gene. Journal of Biological Chemistry 1990;265:20277-84. [DOI: 10.1016/s0021-9258(17)30501-x] [Cited by in Crossref: 43] [Article Influence: 1.4] [Reference Citation Analysis]
95 Stepensky P, Shapira MY, Balashov D, Trakhtman P, Skorobogatova E, Rheingold L, Brooks R, Revel-vilk S, Weintraub M, Stein J, Maschan A, Or R, Resnick IB. Bone Marrow Transplantation for Fanconi Anemia Using Fludarabine-Based Conditioning. Biology of Blood and Marrow Transplantation 2011;17:1282-8. [DOI: 10.1016/j.bbmt.2011.01.001] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 2.8] [Reference Citation Analysis]
96 Giacometti C, Bellan E, Ambrosi A, Dei Tos AP, Cassaro M, Ludwig K. "While there is p57, there is hope." The past and the present of diagnosis in first trimester abortions: Diagnostic dilemmas and algorithmic approaches. A review. Placenta 2021:S0143-4004(21)00060-6. [PMID: 33714612 DOI: 10.1016/j.placenta.2021.02.010] [Reference Citation Analysis]
97 Ho K, Craddock EM, Piano F, Kambysellis MP. Phylogenetic analysis of DNA length mutations in a repetitive region of the Hawaiiandrosophila yolk protein geneYp2. J Mol Evol 1996;43:116-24. [DOI: 10.1007/bf02337356] [Cited by in Crossref: 12] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
98 Leon SP, Zhu J, Black PM. Genetic Aberrations in Human Brain Tumors: . Neurosurgery 1994;34:708-22. [DOI: 10.1227/00006123-199404000-00021] [Cited by in Crossref: 33] [Cited by in F6Publishing: 36] [Article Influence: 1.2] [Reference Citation Analysis]
99 Melmer G. Hybridization of the variable number of tandem repeat core oligonucleotide GNNGTGGG to 350 cosmids from chromosome 7. Electrophoresis 1994;15:175-6. [PMID: 8026431 DOI: 10.1002/elps.1150150130] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
100 de Lange T, Shiue L, Myers RM, Cox DR, Naylor SL, Killery AM, Varmus HE. Structure and variability of human chromosome ends. Mol Cell Biol. 1990;10:518-527. [PMID: 2300052 DOI: 10.1128/mcb.10.2.518] [Cited by in Crossref: 530] [Article Influence: 17.1] [Reference Citation Analysis]
101 Sheen FM, Sherry ST, Risch GM, Robichaux M, Nasidze I, Stoneking M, Batzer MA, Swergold GD. Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition. Genome Res 2000;10:1496-508. [PMID: 11042149 DOI: 10.1101/gr.149400] [Cited by in Crossref: 94] [Cited by in F6Publishing: 88] [Article Influence: 4.7] [Reference Citation Analysis]
102 Takenaka O, Takasaki H, Kawamoto S, Arakawa M, Takenaka A. Polymorphic microsatellite DNA amplification customized for chimpanzee paternity testing. Primates 1993;34:27-35. [DOI: 10.1007/bf02381277] [Cited by in Crossref: 28] [Article Influence: 1.0] [Reference Citation Analysis]
103 Coppieters W, Van De Weghe A, Depicker A, Bouquet Y, Van Zeveren A. A hypervariable pig DNA fragment. Animal Genetics 1990;21:29-38. [DOI: 10.1111/j.1365-2052.1990.tb03204.x] [Cited by in Crossref: 23] [Cited by in F6Publishing: 12] [Article Influence: 2.9] [Reference Citation Analysis]
104 Li C, Yandell DW, Little JB. Evidence for coincident mutations in human lymphoblast clones selected for functional loss of a thymidine kinase gene. Mol Carcinog 1992;5:270-7. [DOI: 10.1002/mc.2940050407] [Cited by in Crossref: 22] [Cited by in F6Publishing: 14] [Article Influence: 0.8] [Reference Citation Analysis]
105 Nakamura Y, Lathrop M, O'connell P, Leppert M, Barker D, Wright E, Skolnick M, Kondoleon S, Litt M, Lalouel J, White R. A mapped set of DNA markers for human chromosome 17. Genomics 1988;2:302-9. [DOI: 10.1016/0888-7543(88)90018-3] [Cited by in Crossref: 83] [Cited by in F6Publishing: 80] [Article Influence: 2.5] [Reference Citation Analysis]
106 Kedmi M, Resnick IB, Dray L, Aker M, Samuel S, Gesundheit B, Slavin S, Or R, Shapira MY. A Retrospective Review of the Outcome after Second or Subsequent Allogeneic Transplantation. Biology of Blood and Marrow Transplantation 2009;15:483-9. [DOI: 10.1016/j.bbmt.2009.01.009] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 2.3] [Reference Citation Analysis]
107 Miny P, Holzgreve W, Horst J. Genetic factors in lissencephaly syndromes: a review. Child's Nerv Syst 1993;9:413-7. [DOI: 10.1007/bf00306195] [Cited by in Crossref: 13] [Article Influence: 0.5] [Reference Citation Analysis]
108 Fondon JW 3rd, Mele GM, Brezinschek RI, Cummings D, Pande A, Wren J, O'Brien KM, Kupfer KC, Wei MH, Lerman M, Minna JD, Garner HR. Computerized polymorphic marker identification: experimental validation and a predicted human polymorphism catalog. Proc Natl Acad Sci U S A 1998;95:7514-9. [PMID: 9636181 DOI: 10.1073/pnas.95.13.7514] [Cited by in Crossref: 39] [Cited by in F6Publishing: 39] [Article Influence: 1.7] [Reference Citation Analysis]
109 Fries R, Beckmann JS, Georges M, Sollero M, Womack J. The bovine gene map. Animal Genetics 1989;20:3-29. [DOI: 10.1111/j.1365-2052.1989.tb00838.x] [Cited by in Crossref: 42] [Cited by in F6Publishing: 21] [Article Influence: 3.5] [Reference Citation Analysis]
110 Feitelson M. Hepatitis B virus infection and primary hepatocellular carcinoma. Clin Microbiol Rev. 1992;5:275-301. [PMID: 1323384 DOI: 10.1128/cmr.5.3.275] [Cited by in Crossref: 56] [Cited by in F6Publishing: 14] [Article Influence: 1.9] [Reference Citation Analysis]
111 Dirks WG, Drexler HG. Online verification of human cell line identity by STR DNA typing. Methods Mol Biol 2011;731:45-55. [PMID: 21516397 DOI: 10.1007/978-1-61779-080-5_5] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 1.7] [Reference Citation Analysis]
112 Armour JA, Jeffreys AJ. Recent advances in minisatellite biology. FEBS Letters 1992;307:113-5. [DOI: 10.1016/0014-5793(92)80912-z] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
113 Barroso G, Sonnenberg AS, Van Griensven LJ, Labarère J. Molecular Cloning of a Widely Distributed Microsatellite Core Sequence from the Cultivated Mushroom Agaricus bisporus. Fungal Genetics and Biology 2000;31:115-23. [DOI: 10.1006/fgbi.2000.1239] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
114 Gendler SJ, Spicer AP, Lalani EN, Duhig T, Peat N, Burchell J, Pemberton L, Boshell M, Taylor-Papadimitriou J. Structure and biology of a carcinoma-associated mucin, MUC1. Am Rev Respir Dis. 1991;144:S42-S47. [PMID: 1892326 DOI: 10.1164/ajrccm/144.3_pt_2.s42] [Cited by in Crossref: 129] [Cited by in F6Publishing: 18] [Article Influence: 4.3] [Reference Citation Analysis]
115 Lothe R, Fosså S, Stenwig A, Nakamura Y, White R, Børresen A, Brøgger A. Loss of 3p or 11p alleles is associated with testicular cancer tumors. Genomics 1989;5:134-8. [DOI: 10.1016/0888-7543(89)90097-9] [Cited by in Crossref: 76] [Cited by in F6Publishing: 71] [Article Influence: 2.4] [Reference Citation Analysis]
116 Da Silva WA, Bortolini MC, Meyer D, Salzano FM, Elion J, Krishnamoorthy R, Schneider MPC, De Guerra DC, Layrisse Z, Castellano HM, Weimer TDA, Zago MA. Genetic diversity of two African and sixteen South American populations determined on the basis of six hypervariable loci. Am J Phys Anthropol 1999;109:425-37. [DOI: 10.1002/(sici)1096-8644(199908)109:4<425::aid-ajpa1>3.0.co;2-d] [Cited by in Crossref: 26] [Cited by in F6Publishing: 3] [Article Influence: 1.2] [Reference Citation Analysis]
117 Brevik ØJ, Ottem KF, Nylund A. Multiple-locus, variable number of tandem repeat analysis (MLVA) of the fish-pathogen Francisella noatunensis. BMC Vet Res 2011;7:5. [PMID: 21261955 DOI: 10.1186/1746-6148-7-5] [Cited by in Crossref: 15] [Cited by in F6Publishing: 8] [Article Influence: 1.5] [Reference Citation Analysis]
118 Rossiter JP, Blakemore KJ, Kickler TS, Kasch LM, Khouzami AN, Pressman EK, Sciscione AC, Kazazian HH. The use of polymerase chain reaction to determine fetal RhD status. American Journal of Obstetrics and Gynecology 1994;171:1047-51. [DOI: 10.1016/0002-9378(94)90032-9] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 0.4] [Reference Citation Analysis]
119 Moyzis RK, Buckingham JM, Cram LS, Dani M, Deaven LL, Jones MD, Meyne J, Ratliff RL, Wu JR. A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes. Proc Natl Acad Sci U S A 1988;85:6622-6. [PMID: 3413114 DOI: 10.1073/pnas.85.18.6622] [Cited by in Crossref: 1398] [Cited by in F6Publishing: 1236] [Article Influence: 42.4] [Reference Citation Analysis]
120 Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M. A second-generation linkage map of the human genome. Nature. 1992;359:794-801. [PMID: 1436057 DOI: 10.1038/359794a0] [Cited by in Crossref: 1064] [Cited by in F6Publishing: 964] [Article Influence: 36.7] [Reference Citation Analysis]
121 Weising K, Beyermann B, Ramser J, Kahl G. Plant DNA fingerprinting with radioactive and digoxigenated oligonucleotide probes complementary to simple repetitive DNA sequences. Electrophoresis 1991;12:159-69. [DOI: 10.1002/elps.1150120211] [Cited by in Crossref: 80] [Cited by in F6Publishing: 36] [Article Influence: 2.7] [Reference Citation Analysis]
122 Korenberg JR, Kawashima H, Pulst SM, Allen L, Magenis E, Epstein CJ. Down syndrome: toward a molecular definition of the phenotype. Am J Med Genet Suppl 1990;7:91-7. [PMID: 2149983 DOI: 10.1002/ajmg.1320370719] [Cited by in Crossref: 6] [Cited by in F6Publishing: 11] [Article Influence: 0.2] [Reference Citation Analysis]
123 Loewy ZG, Pottathil R. Polymerase Chain Reaction and Its Use in Diagnostics. In: Singh P, Sharma BP, Tyle P, editors. Diagnostics in the Year 2000. Dordrecht: Springer Netherlands; 1993. pp. 389-410. [DOI: 10.1007/978-94-011-6976-9_22] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.1] [Reference Citation Analysis]
124 Brinkmann B, Rand S, Bajanowski T. Forensic identification of urine samples. Int J Leg Med 1992;105:59-61. [DOI: 10.1007/bf01371242] [Cited by in Crossref: 42] [Cited by in F6Publishing: 6] [Article Influence: 1.4] [Reference Citation Analysis]
125 Hatano Y, Tamada M, Matsuo M, Hara A. Molecular Trajectory of BRCA1 and BRCA2 Mutations. Front Oncol 2020;10:361. [PMID: 32269964 DOI: 10.3389/fonc.2020.00361] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 17.0] [Reference Citation Analysis]
126 Chen C, Choo K, Cheng WTK. Frequent deletions and sequence aberrations at the transgene junctions of transgenic mice carrying the papillomavirus regulatory and the SV40 TAg gene sequences. Transgenic Research 1995;4:52-9. [DOI: 10.1007/bf01976502] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 0.5] [Reference Citation Analysis]
127 Or R, Hadar E, Bitan M, Resnick IB, Aker M, Ackerstein A, Samuel S, Tsirigotis P, Gesundheit B, Slavin S, Shapira MY. Safety and efficacy of donor lymphocyte infusions following mismatched stem cell transplantation. Biol Blood Marrow Transplant 2006;12:1295-301. [PMID: 17162211 DOI: 10.1016/j.bbmt.2006.07.014] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 1.6] [Reference Citation Analysis]
128 Okuda K. Hepatocellular carcinoma: recent progress. Hepatology. 1992;15:948-963. [PMID: 1314774 DOI: 10.1002/hep.1840150532] [Cited by in Crossref: 367] [Cited by in F6Publishing: 325] [Article Influence: 12.7] [Reference Citation Analysis]
129 Tautz D. Genomic finger printing goes simple. Bioessays 1990;12:44-6. [PMID: 2182003 DOI: 10.1002/bies.950120111] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 0.3] [Reference Citation Analysis]
130 Leibel RL, Bahary N, Friedman JM. Strategies for the molecular genetic analysis of obesity in humans. Crit Rev Food Sci Nutr 1993;33:351-8. [PMID: 8357496 DOI: 10.1080/10408399309527632] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.3] [Reference Citation Analysis]
131 Helminen P, Sajantila A, Johnsson V, Lukka M, Ehnholm C, Peltonen L. Amplification of three hypervariable DNA regions by polymerase chain reaction for paternity determinations: comparison with conventional methods and DNA fingerprinting. Mol Cell Probes 1992;6:21-6. [PMID: 1545830 DOI: 10.1016/0890-8508(92)90067-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
132 Li C, Yandell DW, Little JB. Molecular mechanisms of spontaneous and induced loss of heterozygosity in human cells in vitro. Somat Cell Mol Genet 1992;18:77-87. [DOI: 10.1007/bf01233450] [Cited by in Crossref: 50] [Cited by in F6Publishing: 7] [Article Influence: 1.7] [Reference Citation Analysis]
133 Konopka AK. Compilation of DNA strand exchange sites for non-homologous recombination in somatic cells. Nucleic Acids Res 1988;16:1739-58. [PMID: 2832826 DOI: 10.1093/nar/16.5.1739] [Cited by in Crossref: 52] [Cited by in F6Publishing: 53] [Article Influence: 1.6] [Reference Citation Analysis]
134 O'rahilly S, Wainscoat JS, Turner RC. Type 2 (non-insulin-dependent) diabetes mellitus new genetics for old nightmares. Diabetologia 1988;31:407-14. [DOI: 10.1007/bf00271584] [Cited by in Crossref: 46] [Cited by in F6Publishing: 5] [Article Influence: 1.4] [Reference Citation Analysis]
135 Mignot E, Guilleminault C, Dement WC, Grumet FC. Genetically Determined Animal Models of Narcolepsy, A Disorder of REM Sleep. In: Driscoll P, editor. Genetically Defined Animal Models of Neurobehavioral Dysfunctions. Boston: Birkhäuser; 1992. pp. 89-110. [DOI: 10.1007/978-1-4899-6732-9_5] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.3] [Reference Citation Analysis]
136 Lupski JR, de Oca-luna RM, Slaugenhaupt S, Pentao L, Guzzetta V, Trask BJ, Saucedo-cardenas O, Barker DF, Killian JM, Garcia CA, Chakravarti A, Patel PI. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 1991;66:219-32. [DOI: 10.1016/0092-8674(91)90613-4] [Cited by in Crossref: 889] [Cited by in F6Publishing: 735] [Article Influence: 29.6] [Reference Citation Analysis]
137 Daumer-haas C, Schuffenhauer S, Walther JU, Schipper RD, Porstmann T, Korenberg JR. Tetrasomy 21 pter→q22.1 and Down syndrome: Molecular definition of the region. Am J Med Genet 1994;53:359-65. [DOI: 10.1002/ajmg.1320530411] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 0.6] [Reference Citation Analysis]
138 Deka R, Shriver MD, Yu LM, Ferrell RE, Chakraborty R. Intra- and inter-population diversity at short tandem repeat loci in diverse populations of the world. Electrophoresis 1995;16:1659-64. [PMID: 8582352 DOI: 10.1002/elps.11501601275] [Cited by in Crossref: 46] [Cited by in F6Publishing: 36] [Article Influence: 1.8] [Reference Citation Analysis]
139 Pena SD, de Souza KT, de Andrade M, Chakraborty R. Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene. Proc Natl Acad Sci U S A 1994;91:723-7. [PMID: 8290589 DOI: 10.1073/pnas.91.2.723] [Cited by in Crossref: 20] [Cited by in F6Publishing: 15] [Article Influence: 0.7] [Reference Citation Analysis]
140 Hyytiä-trees E, Smole SC, Fields PA, Swaminathan B, Ribot EM. Second Generation Subtyping: A Proposed PulseNet Protocol for Multiple-Locus Variable-Number Tandem Repeat Analysis of Shiga Toxin–Producing Escherichia coli O157 (STEC O157). Foodborne Pathogens and Disease 2006;3:118-31. [DOI: 10.1089/fpd.2006.3.118] [Cited by in Crossref: 135] [Cited by in F6Publishing: 83] [Article Influence: 9.0] [Reference Citation Analysis]
141 Chang HR, Ishizaki K, Sasaki MS, Toguchida J, Kato M, Nakamura Y, Kawamura S, Moriguchi T, Ikenaga M. Somatic mosaicism for DNA repair capacity in fibroblasts derived from a group A xeroderma pigmentosum patient. J Invest Dermatol 1989;93:460-5. [PMID: 2570806 DOI: 10.1111/1523-1747.ep12284030] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.3] [Reference Citation Analysis]
142 Wu KS, Tanksley SD. Abundance, polymorphism and genetic mapping of microsatellites in rice. Mol Gen Genet 1993;241:225-35. [PMID: 7901751 DOI: 10.1007/BF00280220] [Cited by in Crossref: 179] [Cited by in F6Publishing: 74] [Article Influence: 6.4] [Reference Citation Analysis]
143 Mitani K, Takahashi Y, Kominami R. A GGCAGG motif in minisatellites affecting their germline instability. Journal of Biological Chemistry 1990;265:15203-10. [DOI: 10.1016/s0021-9258(18)77242-6] [Cited by in Crossref: 50] [Article Influence: 1.6] [Reference Citation Analysis]
144 Saha A, Husain S, Bamezai R. Characterization of a Subcloned Fragment (pBA0.6) of pCMM86 Located on 17q21 and Its Potential Use in Generating an Individual-Specific DNA Profile. DNA and Cell Biology 2000;19:219-26. [DOI: 10.1089/104454900314483] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
145 Nagler A, Slavin S, Varadi G, Naparstek E, Samuel S, Or R. Allogeneic peripheral blood stem cell transplantation using a fludarabine-based low intensity conditioning regimen for malignant lymphoma. Bone Marrow Transplant 2000;25:1021-8. [PMID: 10828860 DOI: 10.1038/sj.bmt.1702392] [Cited by in Crossref: 142] [Cited by in F6Publishing: 116] [Article Influence: 6.8] [Reference Citation Analysis]
146 Soller M. Genetic Mapping of the Bovine Genome Using Deoxyribonucleic Acid-Level Markers to Identify Loci Affecting Quantitative Traits of Economic Importance. Journal of Dairy Science 1990;73:2628-46. [DOI: 10.3168/jds.s0022-0302(90)78949-7] [Cited by in Crossref: 31] [Article Influence: 1.0] [Reference Citation Analysis]
147 Yamakawa K, Takahashi E, Saito H, Sato T, Oshimura M, Hori T, Nakamura Y. Isolation and mapping of 75 new DNA markers on human chromosome 3. Genomics 1991;9:536-43. [DOI: 10.1016/0888-7543(91)90421-a] [Cited by in Crossref: 22] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
148 Murtagh JJ Jr, Eddy R, Shows TB, Moss J, Vaughan M. Different forms of Go alpha mRNA arise by alternative splicing of transcripts from a single gene on human chromosome 16. Mol Cell Biol 1991;11:1146-55. [PMID: 1899283 DOI: 10.1128/mcb.11.2.1146-1155.1991] [Cited by in Crossref: 17] [Article Influence: 0.6] [Reference Citation Analysis]
149 de Gouyon B, Julier C, Avner P, Georges M, Lathrop M. Human variable number of tandem repeat probes as a source of polymorphic markers in experimental animals. EXS 1991;58:85-94. [PMID: 1831168 DOI: 10.1007/978-3-0348-7312-3_6] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
150 King MC. "The race" to clone BRCA1. Science 2014;343:1462-5. [PMID: 24675952 DOI: 10.1126/science.1251900] [Cited by in Crossref: 49] [Cited by in F6Publishing: 34] [Article Influence: 7.0] [Reference Citation Analysis]
151 Royle NJ. The proterminal regions and telomeres of human chromosomes. Adv Genet 1995;32:273-315. [PMID: 7741024 DOI: 10.1016/s0065-2660(08)60207-2] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
152 Harding RM. VNTRs in review. Evol Anthropol 1992;1:62-71. [DOI: 10.1002/evan.1360010208] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
153 Knight A, Dyson P. Detection of DNA polymorphisms between two inbred mouse strains—limitations of restriction fragment length polymorphisms (RFLPs). Molecular and Cellular Probes 1990;4:497-504. [DOI: 10.1016/0890-8508(90)90008-n] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
154 Resnick IB, Abdul Hai A, Shapira MY, Bitan M, Hershkovitz E, Schwartz A, Ben-harush M, Or R, Slavin S, Kapelushnik J. Treatment of X-linked childhood cerebral adrenoleukodystrophy by the use of an allogeneic stem cell transplantation with reduced intensity conditioning regimen: Reduced intensity BMT for adrenoleukodystrophy. Clinical Transplantation 2005;19:840-7. [DOI: 10.1111/j.1399-0012.2005.00411.x] [Cited by in Crossref: 19] [Cited by in F6Publishing: 13] [Article Influence: 1.2] [Reference Citation Analysis]
155 Rogstad SH. [20] Surveying plant genomes for variable number of tandem repeat loci. Molecular Evolution: Producing the Biochemical Data. Elsevier; 1993. pp. 278-94. [DOI: 10.1016/0076-6879(93)24021-l] [Cited by in Crossref: 23] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
156 Williams RC. Restriction fragment length polymorphism (RFLP). Am J Phys Anthropol 1989;32:159-84. [DOI: 10.1002/ajpa.1330320508] [Cited by in Crossref: 11] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
157 Goodwin SB, Drenth A, Fry WE. Cloning and genetic analyses of two highly polymorphic, moderately repetitive nuclear DNAs from Phytophthora infestans. Curr Genet 1992;22:107-15. [DOI: 10.1007/bf00351469] [Cited by in Crossref: 216] [Cited by in F6Publishing: 19] [Article Influence: 7.4] [Reference Citation Analysis]
158 Kamatani Y, Nakamura Y. Genetic variations in medical research in the past, at present and in the future. Proc Jpn Acad Ser B Phys Biol Sci 2021;97:324-35. [PMID: 34121043 DOI: 10.2183/pjab.97.018] [Reference Citation Analysis]
159 Frediani M, Maggini F, Gelati M, Cremonini R. Repetitive DNA sequences as probes for phylogenetic analysis in Vicia genus. Caryologia 2014;57:379-86. [DOI: 10.1080/00087114.2004.10589420] [Cited by in Crossref: 10] [Cited by in F6Publishing: 3] [Article Influence: 1.4] [Reference Citation Analysis]
160 Horowitz JM, Park SH, Bogenmann E, Cheng JC, Yandell DW, Kaye FJ, Minna JD, Dryja TP, Weinberg RA. Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells. Proc Natl Acad Sci U S A 1990;87:2775-9. [PMID: 2181449 DOI: 10.1073/pnas.87.7.2775] [Cited by in Crossref: 320] [Cited by in F6Publishing: 301] [Article Influence: 10.3] [Reference Citation Analysis]
161 Sonnante G, Stockton T, Nodari RO, Becerra Velásquez VL, Gepts P. Evolution of genetic diversity during the domestication of common-bean (Phaseolus vulgaris L.). Theor Appl Genet 1994;89:629-35. [PMID: 24177940 DOI: 10.1007/BF00222458] [Cited by in Crossref: 77] [Cited by in F6Publishing: 21] [Article Influence: 9.6] [Reference Citation Analysis]
162 Mohrenweiser HW, D. Larsen R, Neel JV. Development of molecular approaches to estimating germinal mutation rates I. Detection of insertion/deletion/rearrangement variants in the human genome. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 1989;212:241-52. [DOI: 10.1016/0027-5107(89)90075-4] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 0.5] [Reference Citation Analysis]
163 Kass DH, Aleman C, Batzer MA, Deininger PL. Identification of a human specific Alu insertion in the factor XIIIB gene. Genetica 1994;94:1-8. [PMID: 7729692 DOI: 10.1007/BF01429214] [Cited by in Crossref: 18] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
164 Lewis PO, Snow AA. Deterministic paternity exclusion using RAPD markers. Mol Ecol 1992;1:155-60. [DOI: 10.1111/j.1365-294x.1992.tb00171.x] [Cited by in Crossref: 34] [Cited by in F6Publishing: 2] [Article Influence: 1.2] [Reference Citation Analysis]
165 Goy A, Passalaris T, Xiao YH, Miller WH Jr, Siegel DS, Zelenetz AD. The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphism. Genomics 1995;26:327-33. [PMID: 7601459 DOI: 10.1016/0888-7543(95)80217-a] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
166 Makos M, Nelkin BD, Lerman MI, Latif F, Zbar B, Baylin SB. Distinct hypermethylation patterns occur at altered chromosome loci in human lung and colon cancer. Proc Natl Acad Sci U S A 1992;89:1929-33. [PMID: 1347428 DOI: 10.1073/pnas.89.5.1929] [Cited by in Crossref: 95] [Cited by in F6Publishing: 80] [Article Influence: 3.3] [Reference Citation Analysis]
167 Le Roux MG, Pascal O, Andre MT, Herbert O, David A, Moisan JP. Non-paternity and genetic counselling. Lancet 1992;340:607. [PMID: 1355175 DOI: 10.1016/0140-6736(92)92139-7] [Cited by in Crossref: 22] [Cited by in F6Publishing: 11] [Article Influence: 0.8] [Reference Citation Analysis]
168 Uitterlinden AG, Slagboom EP, Mullaart E, Meulenbelt I, Vijg J. Genome scanning by two-dimensional DNA typing: The use of repetitive DNA sequences for rapid mapping of genetic traits. Electrophoresis 1991;12:119-34. [DOI: 10.1002/elps.1150120206] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 0.4] [Reference Citation Analysis]
169 Hanotte O, Burke T, Armour JA, Jeffreys AJ. Hypervariable minisatellite DNA sequences in the Indian peafowl Pavo cristatus. Genomics 1991;9:587-97. [DOI: 10.1016/0888-7543(91)90351-e] [Cited by in Crossref: 48] [Cited by in F6Publishing: 2] [Article Influence: 1.6] [Reference Citation Analysis]
170 Vos P, Hogers R, Bleeker M, Reijans M, van de Lee T, Hornes M, Frijters A, Pot J, Peleman J, Kuiper M. AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res 1995;23:4407-14. [PMID: 7501463 DOI: 10.1093/nar/23.21.4407] [Cited by in Crossref: 7903] [Cited by in F6Publishing: 3736] [Article Influence: 316.1] [Reference Citation Analysis]
171 Meuwissen T, Van Arendonk J. Potential Improvements in Rate of Genetic Gain from Marker-Assisted Selection in Dairy Cattle Breeding Schemes. Journal of Dairy Science 1992;75:1651-9. [DOI: 10.3168/jds.s0022-0302(92)77922-3] [Cited by in Crossref: 63] [Cited by in F6Publishing: 1] [Article Influence: 2.2] [Reference Citation Analysis]
172 Kesawat MS, Das Kumar B. Molecular markers: It’s application in crop improvement. J Crop Sci Biotechnol 2009;12:169-81. [DOI: 10.1007/s12892-009-0124-6] [Cited by in Crossref: 42] [Cited by in F6Publishing: 4] [Article Influence: 3.8] [Reference Citation Analysis]
173 Wang W, Bittles AH. Imperfect units of an extended microsatellite structure involving single nucleotide changes. Electrophoresis 2001;22:1095-7. [PMID: 11358131 DOI: 10.1002/1522-2683()22:6<1095::AID-ELPS1095>3.0.CO;2-A] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
174 Karama M, Gyles CL. Methods for genotyping verotoxin-producing Escherichia coli. Zoonoses Public Health 2010;57:447-62. [PMID: 19912610 DOI: 10.1111/j.1863-2378.2009.01259.x] [Cited by in Crossref: 27] [Cited by in F6Publishing: 16] [Article Influence: 2.7] [Reference Citation Analysis]
175 White P, Tatum OL, Deaven LL, Longmire JL. New, Male-Specific Microsatellite Markers from the Human Y Chromosome. Genomics 1999;57:433-7. [DOI: 10.1006/geno.1999.5782] [Cited by in Crossref: 75] [Cited by in F6Publishing: 45] [Article Influence: 3.4] [Reference Citation Analysis]
176 Ann DK, Smith MK, Carlson DM. Molecular evolution of the mouse proline-rich protein multigene family. Insertion of a long interspersed repeated DNA element. Journal of Biological Chemistry 1988;263:10887-93. [DOI: 10.1016/s0021-9258(18)38053-0] [Cited by in Crossref: 26] [Article Influence: 0.8] [Reference Citation Analysis]
177 Ndifon W, Nkwanta A, Hill D. Some probabilistic results on the nonrandomness of simple sequence repeats in DNA sequences. Bull Math Biol 2006;68:1747-59. [PMID: 16847719 DOI: 10.1007/s11538-005-9029-9] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
178 Martin PD, Schmitter H, Schneider PM. A brief history of the formation of DNA databases in forensic science within Europe. Forensic Science International 2001;119:225-31. [DOI: 10.1016/s0379-0738(00)00436-9] [Cited by in Crossref: 62] [Cited by in F6Publishing: 10] [Article Influence: 3.1] [Reference Citation Analysis]
179 Dudley CR, Giuffra LA, Tippett P, Kidd KK, Reeders ST. The Na+/H+ antiporter: a "melt" polymorphism allows regional mapping to the short arm of chromosome 1. Hum Genet 1990;86:79-83. [PMID: 1979310 DOI: 10.1007/BF00205179] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
180 Bowcock AM, Ray A, Erlich HA, Sehgal PB. The Molecular Genetics of Beta-2 Interferon/Interleukin-6 (IFNβ2/IL6)a. Annals of the New York Academy of Sciences 1989;557:345-52. [DOI: 10.1111/j.1749-6632.1989.tb24027.x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
181 Purdie CA, Piris J, Bird CC, Wyllie AH. 17q allele loss is associated with lymph node metastasis in locally aggressive human colorectal cancer. J Pathol 1995;175:297-302. [DOI: 10.1002/path.1711750307] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 0.3] [Reference Citation Analysis]
182 Georges M, Gunawardana A, Threadgill DW, Lathrop M, Olsaker I, Mishra A, Sargeant LL, Schoeberlein A, Steele MR, Terry C. Characterization of a set of variable number of tandem repeat markers conserved in bovidae. Genomics 1991;11:24-32. [PMID: 1765384 DOI: 10.1016/0888-7543(91)90098-y] [Cited by in Crossref: 43] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
183 Gill P, Woodroffe S, Lygo JE, Millican ES. Population genetics of four hypervariable loci. Int J Legal Med 1991;104:221-7. [PMID: 1931739 DOI: 10.1007/BF01369811] [Cited by in Crossref: 25] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
184 Myers JS, Vincent BJ, Udall H, Watkins WS, Morrish TA, Kilroy GE, Swergold GD, Henke J, Henke L, Moran JV, Jorde LB, Batzer MA. A comprehensive analysis of recently integrated human Ta L1 elements. Am J Hum Genet 2002;71:312-26. [PMID: 12070800 DOI: 10.1086/341718] [Cited by in Crossref: 96] [Cited by in F6Publishing: 105] [Article Influence: 5.1] [Reference Citation Analysis]
185 Oostra BA, de Rijk-van Andel JF, Eussen HJ, van Hemel JO, Halley DJJ, Niermeijer MF. DNA analysis in patients with lissencephaly type I and other cortical dysplasias. Am J Med Genet 1991;40:383-6. [DOI: 10.1002/ajmg.1320400328] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.1] [Reference Citation Analysis]
186 Krajči P, Gedde-dahl T, Høyheim B, Rogde S, Olaisen B, Brandtzaeg P. The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1. Hum Genet 1992;90:215-9. [DOI: 10.1007/bf00220065] [Cited by in Crossref: 13] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
187 Itoh T, Yamaizumi M. UVs syndrome: establishment and characterization of fibroblastic cell lines transformed with simian virus 40 DNA. J Invest Dermatol 2000;114:101-6. [PMID: 10620123 DOI: 10.1046/j.1523-1747.2000.00843.x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.4] [Reference Citation Analysis]
188 Zhou X, Zhu J, Sun H, Shao L, Xu M, Guo H. Family haploidentical donor-derived cytokine-induced killer cell biotherapy combined with bortezomib in two patients with relapsed multiple myeloma in a non-allogeneic transplant setting. Leuk Lymphoma 2013;54:209-11. [PMID: 22734810 DOI: 10.3109/10428194.2012.701741] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 1.1] [Reference Citation Analysis]
189 Ostrer H, Hejtmancik JF. Prenatal diagnosis and carrier detection of genetic diseases by analysis of deoxyribonucleic acid. The Journal of Pediatrics 1988;112:679-87. [DOI: 10.1016/s0022-3476(88)80682-6] [Cited by in Crossref: 15] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
190 Tefferi A. Genomics Basics: DNA Structure, Gene Expression, Cloning, Genetic Mapping, and Molecular Tests. Semin Cardiothorac Vasc Anesth 2006;10:282-90. [DOI: 10.1177/1089253206294343] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
191 Apuya NR, Frazier BL, Keim P, Jill Roth E, Lark KG. Restriction fragment length polymorphisms as genetic markers in soybean, Glycine max (L.) merrill. Theoret Appl Genetics 1988;75:889-901. [DOI: 10.1007/bf00258050] [Cited by in Crossref: 120] [Article Influence: 3.6] [Reference Citation Analysis]
192 Kashi Y, Hallerman E, Soller M. Marker-assisted selection of candidate bulls for progeny testing programmes. Anim Sci 1990;51:63-74. [DOI: 10.1017/s0003356100005158] [Cited by in Crossref: 74] [Article Influence: 6.7] [Reference Citation Analysis]
193 Nakamura Y, Cowen J, Krapcho K, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence pJCZ3.1 on chromosome 19 [D19S20]. Nucleic Acids Res 1988;16:1229. [PMID: 2894014 DOI: 10.1093/nar/16.3.1229] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
194 Villalba M, Ferrari D, Bozza A, Del Senno L, Di Virgilio F. Ionic regulation of endonuclease activity in PC12 cells. Biochem J 1995;311 ( Pt 3):1033-8. [PMID: 7487921 DOI: 10.1042/bj3111033] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.3] [Reference Citation Analysis]
195 Taranenko NI, Potter NT, Allman SL, Golovlev V, Chen C. Detection of trinucleotide expansion in neurodegenerative disease by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Genetic Analysis: Biomolecular Engineering 1999;15:25-31. [DOI: 10.1016/s1050-3862(98)00034-5] [Cited by in Crossref: 15] [Article Influence: 0.7] [Reference Citation Analysis]
196 Thomas MR, Matsumoto S, Cain P, Scott NS. Repetitive DNA of grapevine: classes present and sequences suitable for cultivar identification. Theor Appl Genet 1993;86:173-80. [PMID: 24193457 DOI: 10.1007/BF00222076] [Cited by in Crossref: 95] [Cited by in F6Publishing: 28] [Article Influence: 11.9] [Reference Citation Analysis]
197 Gyllensten UB, Jakobsson S, Temrin H, Wilson AC. Nucleotide sequence and genomic organization of bird minisatellites. Nucleic Acids Res 1989;17:2203-14. [PMID: 2704618 DOI: 10.1093/nar/17.6.2203] [Cited by in Crossref: 42] [Cited by in F6Publishing: 18] [Article Influence: 1.3] [Reference Citation Analysis]
198 Fredholm M, Winter� AK, Christensen K, Kristensen B, Nielsen PB, Davies W, Archibald A. Characterization of 24 porcine (dA-dC)n-(dT-dG)n microsatellites: genotyping of unrelated animals from four breeds and linkage studies. Mammalian Genome 1993;4:187-92. [DOI: 10.1007/bf00417561] [Cited by in Crossref: 60] [Cited by in F6Publishing: 4] [Article Influence: 2.1] [Reference Citation Analysis]
199 Neitzel H, Digweed M, Nürnberg P, Pöpperl A, Schmidt CA, Tinschert S, Sperling K. Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5. Clinical Genetics 1991;39:97-103. [DOI: 10.1111/j.1399-0004.1991.tb02994.x] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
200 O'connell P, Lathrop G, Nakamura Y, Leppert M, Ardinger R, Murray J, Lalouel J, White R. Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. Genomics 1989;4:12-20. [DOI: 10.1016/0888-7543(89)90308-x] [Cited by in Crossref: 56] [Cited by in F6Publishing: 5] [Article Influence: 1.8] [Reference Citation Analysis]
201 Longmire JL, Lewis AK, Brown NC, Buckingham JM, Clark LM, Jones MD, Meincke LJ, Meyne J, Ratliff RL, Ray F, Wagner RP, Moyzis RK. Isolation and molecular characterization of a highly polymorphic centromeric tandem repeat in the family falconidae. Genomics 1988;2:14-24. [DOI: 10.1016/0888-7543(88)90104-8] [Cited by in Crossref: 211] [Cited by in F6Publishing: 87] [Article Influence: 6.4] [Reference Citation Analysis]
202 Cebula TA, Jackson SA, Brown EW, Goswami B, Leclerc JE. Chips and SNPs, Bugs and Thugs: A Molecular Sleuthing Perspective. Journal of Food Protection 2005;68:1271-84. [DOI: 10.4315/0362-028x-68.6.1271] [Cited by in Crossref: 20] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
203 Nancarrow DJ, Palmer JM, Walters MK, Kerr BM, Hafner GJ, Garske L, Mcleod G, Hayward NK. Exclusion of the familial melanoma locus (MLM) from the PNDD1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees. Genomics 1992;12:18-25. [DOI: 10.1016/0888-7543(92)90401-d] [Cited by in Crossref: 31] [Cited by in F6Publishing: 4] [Article Influence: 1.1] [Reference Citation Analysis]
204 Weissenbach J. Microsatellite polymorphisms and the genetic linkage map of the human genome. Current Opinion in Genetics & Development 1993;3:414-7. [DOI: 10.1016/0959-437x(93)90114-5] [Cited by in Crossref: 23] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
205 Tang JQ, Korab-laskowska M, Jarnik M, Cardinal G, Vanasse M, Melan�on SB, Labuda D. Alu-PCR combined with non-Alu primers reveals multiple polymorphic loci. Mammalian Genome 1995;6:345-9. [DOI: 10.1007/bf00364798] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
206 Shekar M, Acharya S, Karunasagar I, Karunasagar I. Variable repeat regions in the genome of Vibrio vulnificus and polymorphism in one of the loci in strains isolated from oysters. Int J Food Microbiol 2008;123:240-5. [PMID: 18374439 DOI: 10.1016/j.ijfoodmicro.2008.02.008] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
207 Inukai T. Role of transposable elements in the propagation of minisatellites in the rice genome. Mol Genet Genomics 2004;271:220-7. [PMID: 14760520 DOI: 10.1007/s00438-003-0973-5] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 0.5] [Reference Citation Analysis]
208 Jeffreys AJ, Pena SDJ. Brief introduction to human DNA fingerprinting. In: Pena SDJ, Chakraborty R, Epplen JT, Jeffreys AJ, editors. DNA Fingerprinting: State of the Science. Basel: Birkhäuser; 1993. pp. 1-20. [DOI: 10.1007/978-3-0348-8583-6_1] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 0.4] [Reference Citation Analysis]
209 Tynan KM, Hoar DI. Primate evolution of a human chromosome 1 hypervariable repetitive element. J Mol Evol 1989;28:212-9. [DOI: 10.1007/bf02102478] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
210 Vergnaud G, Mariat D, Apiou F, Aurias A, Lathrop M, Lauthier V. The use of synthetic tandem repeats to isolate new VNTR loci: Cloning of a human hypermutable sequence. Genomics 1991;11:135-44. [DOI: 10.1016/0888-7543(91)90110-z] [Cited by in Crossref: 87] [Cited by in F6Publishing: 16] [Article Influence: 2.9] [Reference Citation Analysis]
211 Kanai Y, Ushijima S, Ochiai A, Eguchi K, Hui A, Hirohashi S. DNA hypermethylation at the D17S5 locus is associated with gastric carcinogenesis. Cancer Lett. 1998;122:135-141. [PMID: 9464502 DOI: 10.1016/s0304-3835(97)00380-7] [Cited by in Crossref: 41] [Cited by in F6Publishing: 14] [Article Influence: 1.8] [Reference Citation Analysis]
212 MacLeod A, Turner CM, Tait A. A high level of mixed Trypanosoma brucei infections in tsetse flies detected by three hypervariable minisatellites. Mol Biochem Parasitol 1999;102:237-48. [PMID: 10498180 DOI: 10.1016/s0166-6851(99)00101-2] [Cited by in Crossref: 51] [Cited by in F6Publishing: 17] [Article Influence: 2.3] [Reference Citation Analysis]
213 Nakamura Y, Fujimoto E, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence pEFD126.3 on chromosome 9q (D9S7). Nucleic Acids Res 1987;15:10607. [PMID: 2892177 DOI: 10.1093/nar/15.24.10607] [Cited by in Crossref: 7] [Cited by in F6Publishing: 11] [Article Influence: 0.2] [Reference Citation Analysis]
214 Sun R, Spain TA, Lin SF, Miller G. Autoantigenic proteins that bind recombinogenic sequences in Epstein-Barr virus and cellular DNA. Proc Natl Acad Sci U S A 1994;91:8646-50. [PMID: 8078938 DOI: 10.1073/pnas.91.18.8646] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 0.4] [Reference Citation Analysis]
215 Inoue M, Takenaka A, Tanaka S, Kominami R, Takenaka O. Paternity discrimination in a Japanese macaque group by DNA fingerprinting. Primates 1990;31:563-70. [DOI: 10.1007/bf02382539] [Cited by in Crossref: 34] [Article Influence: 1.1] [Reference Citation Analysis]
216 . Evolutionary transience of hypervariable minisatellites in man and the primates. Proc R Soc Lond B 1997;243:241-53. [DOI: 10.1098/rspb.1991.0038] [Cited by in Crossref: 46] [Cited by in F6Publishing: 33] [Article Influence: 1.9] [Reference Citation Analysis]
217 O'Dell SD, Chen X, Day IN. Higher resolution microplate array diagonal gel electrophoresis: application to a multiallelic minisatellite. Hum Mutat 2000;15:565-76. [PMID: 10862086 DOI: 10.1002/1098-1004(200006)15:6<565::AID-HUMU8>3.0.CO;2-7] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
218 Rahat MA, Fry M. Purification and characterization of p27, a protein from hepatocyte chromatin. Evidence suggesting that it binds selectively to guanine-rich single-stranded DNA. FEBS Lett 1993;334:60-4. [PMID: 8224228 DOI: 10.1016/0014-5793(93)81680-x] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
219 Consalez G, Stayton CL, Freimer NB, Goonewardena P, Brown W, Gilliam T, Warren ST. Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28. Genomics 1992;12:710-4. [DOI: 10.1016/0888-7543(92)90299-8] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.2] [Reference Citation Analysis]
220 Derom C, Vlietinck R, Derom R, Boklage C, Thiery M, Van den Berghe H. Genotyping of macerated stillborn fetuses. American Journal of Obstetrics and Gynecology 1991;164:797-800. [DOI: 10.1016/0002-9378(91)90518-v] [Cited by in Crossref: 18] [Article Influence: 0.6] [Reference Citation Analysis]
221 Bora PS, Lange LG. Molecular Mechanism of Ethanol Metabolism by Human Brain to Fatty Acid Ethyl Esters. Alcoholism Clin Exp Res 1993;17:28-30. [DOI: 10.1111/j.1530-0277.1993.tb00721.x] [Cited by in Crossref: 35] [Cited by in F6Publishing: 31] [Article Influence: 1.3] [Reference Citation Analysis]
222 Schmitz N, Suttorp M, Schlegelberger B, Weber-matthiesen K, Tiemann M, Sonnen R. THE ROLE OF THE SPLEEN AFTER BONE MARROW TRANSPLANTATION FOR PRIMARY MYELOFIBROSIS. Br J Haematol 1992;81:616-8. [DOI: 10.1111/j.1365-2141.1992.tb03004.x] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.2] [Reference Citation Analysis]
223 Osada H, Kawata M, Yamada M, Okumura K, Takamizawa H. Genetic identification of pregnancies responsible for choriocarcinomas after multiple pregnancies by restriction fragment length polymorphism analysis. American Journal of Obstetrics and Gynecology 1991;165:682-8. [DOI: 10.1016/0002-9378(91)90309-f] [Cited by in Crossref: 22] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
224 Meltzer SJ, Yin J, Huang Y, McDaniel TK, Newkirk C, Iseri O, Vogelstein B, Resau JH. Reduction to homozygosity involving p53 in esophageal cancers demonstrated by the polymerase chain reaction. Proc Natl Acad Sci U S A 1991;88:4976-80. [PMID: 2052580 DOI: 10.1073/pnas.88.11.4976] [Cited by in Crossref: 78] [Cited by in F6Publishing: 76] [Article Influence: 2.6] [Reference Citation Analysis]
225 Slavin S, Nagler A, Naparstek E, Kapelushnik Y, Aker M, Cividalli G, Varadi G, Kirschbaum M, Ackerstein A, Samuel S, Amar A, Brautbar C, Ben-tal O, Eldor A, Or R. Nonmyeloablative Stem Cell Transplantation and Cell Therapy as an Alternative to Conventional Bone Marrow Transplantation With Lethal Cytoreduction for the Treatment of Malignant and Nonmalignant Hematologic Diseases. Blood 1998;91:756-63. [DOI: 10.1182/blood.v91.3.756] [Cited by in Crossref: 1620] [Article Influence: 70.4] [Reference Citation Analysis]
226 Asensio Gil L. PCR-based methods for fish and fishery products authentication. Trends in Food Science & Technology 2007;18:558-66. [DOI: 10.1016/j.tifs.2007.04.016] [Cited by in Crossref: 78] [Cited by in F6Publishing: 40] [Article Influence: 5.6] [Reference Citation Analysis]
227 Nakamura Y, Fujimoto E, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pEFD64.2) on chromosome 3 [D3S46]. Nucleic Acids Res 1988;16:9354. [PMID: 2902581 DOI: 10.1093/nar/16.19.9354] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
228 Fey MF, Hesketh C, Wainscoat JS, Gendler S, Thein SL. Clonal allele loss in gastrointestinal cancers. Br J Cancer 1989;59:750-4. [PMID: 2736209 DOI: 10.1038/bjc.1989.157] [Cited by in Crossref: 26] [Cited by in F6Publishing: 35] [Article Influence: 0.8] [Reference Citation Analysis]
229 Epstein ND, Fananapazir L, Lin HJ, Mulvihill J, White R, Lalouel JM, Lifton RP, Nienhuis AW, Leppert M. Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy. Circulation 1992;85:635-47. [PMID: 1735158 DOI: 10.1161/01.cir.85.2.635] [Cited by in Crossref: 37] [Cited by in F6Publishing: 13] [Article Influence: 1.3] [Reference Citation Analysis]
230 Feuk L, Marshall CR, Wintle RF, Scherer SW. Structural variants: changing the landscape of chromosomes and design of disease studies. Hum Mol Genet 2006;15 Spec No 1:R57-66. [PMID: 16651370 DOI: 10.1093/hmg/ddl057] [Cited by in Crossref: 174] [Cited by in F6Publishing: 132] [Article Influence: 11.6] [Reference Citation Analysis]
231 Silberman JD, Sarver SK, Walsh PJ. Mitochondrial DNA variation and population structure in the spiny lobster Panulirus argus. Marine Biology 1994;120:601-8. [DOI: 10.1007/bf00350081] [Cited by in Crossref: 76] [Article Influence: 2.8] [Reference Citation Analysis]
232 Griffin TJ, Smith LM. Genetic identification by mass spectrometric analysis of single-nucleotide polymorphisms: ternary encoding of genotypes. Anal Chem 2000;72:3298-302. [PMID: 10939403 DOI: 10.1021/ac991390e] [Cited by in Crossref: 28] [Cited by in F6Publishing: 16] [Article Influence: 1.3] [Reference Citation Analysis]
233 Shapira MY, Abdul-hai A, Resnick IB, Bitan M, Tsirigotis P, Aker M, Gesundheit B, Slavin S, Or R. Alefacept treatment for refractory chronic extensive GVHD. Bone Marrow Transplant 2009;43:339-43. [DOI: 10.1038/bmt.2008.324] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 1.9] [Reference Citation Analysis]
234 Akane A, Matsubara K, Shiono H, Yamada M, Nakagome Y. Diagnosis of twin zygosity by hypervariable RFLP markers. Am J Med Genet 1991;41:96-8. [DOI: 10.1002/ajmg.1320410123] [Cited by in Crossref: 19] [Cited by in F6Publishing: 11] [Article Influence: 0.6] [Reference Citation Analysis]
235 Schwartz RC, Blanton SH, Hyde CA, Sottile TR Jr, Hudgins L, Sarfarazi M, Tsipouras P. Linkage analysis in Marfan syndrome. J Med Genet 1990;27:86-90. [PMID: 1969490 DOI: 10.1136/jmg.27.2.86] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.2] [Reference Citation Analysis]
236 Slavin S, Ackerstein A, Or R, Shapira MY, Gesundheit B, Askenasy N, Morecki S. Immunotherapy in high-risk chemotherapy-resistant patients with metastatic solid tumors and hematological malignancies using intentionally mismatched donor lymphocytes activated with rIL-2: a phase I study. Cancer Immunol Immunother 2010;59:1511-9. [PMID: 20563804 DOI: 10.1007/s00262-010-0878-1] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 1.2] [Reference Citation Analysis]
237 Nakamura Y, Cowen J, Myers R, Ballard L, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pJCZ67) on chromosome 7 [D7S396]. Nucleic Acids Res 1988;16:4191. [PMID: 2453851 DOI: 10.1093/nar/16.9.4191] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
238 King MP, Attardi G. Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA. Cell 1988;52:811-9. [DOI: 10.1016/0092-8674(88)90423-0] [Cited by in Crossref: 174] [Cited by in F6Publishing: 153] [Article Influence: 5.3] [Reference Citation Analysis]
239 Järvelä I, Santavuori P, Puhakka L, Haltia M, Peltonen L. Linkage map of the chromosomal region surrounding the infantile neuronal ceroid lipofuscinosis on 1p. Am J Med Genet 1992;42:546-8. [DOI: 10.1002/ajmg.1320420425] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 0.6] [Reference Citation Analysis]
240 Ogata M, Mattern R, Schneider PM, Schacker U, Kaufmann T, Rittner C. Quantitative and qualitative analysis of DNA extracted from postmortem muscle tissues. Z Rechtsmed 1990;103:397-406. [PMID: 1974101 DOI: 10.1007/BF01263148] [Cited by in Crossref: 16] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
241 Smith M, Smalley S, Cantor R, Pandolfo M, Gomez M, Baumann R, Flodman P, Yoshiyama K, Nakamura Y, Julier C, Dumars K, Haines J, Trofatter J, Spence M, Weeks D, Conneally M. Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23. Genomics 1990;6:105-14. [DOI: 10.1016/0888-7543(90)90454-3] [Cited by in Crossref: 77] [Cited by in F6Publishing: 61] [Article Influence: 2.5] [Reference Citation Analysis]
242 Nakamura Y, Martin C, Myers R, Ballard L, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pCMM86) on chromosome 17q [D17S74]. Nucleic Acids Res 1988;16:5223. [PMID: 2898763 DOI: 10.1093/nar/16.11.5223] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 0.4] [Reference Citation Analysis]
243 Fang DC, Yang SM, Zhou XD, Wang DX, Luo YH. Telomere erosion is independent of microsatellite instability but related to loss of heterozygosity in gastric cancer. World J Gastroenteol. 2001;7:522-526. [DOI: 10.3748/wjg.v7.i4.522] [Cited by in CrossRef: 25] [Cited by in F6Publishing: 26] [Article Influence: 1.3] [Reference Citation Analysis]
244 Pinkel D, Landegent J, Collins C, Fuscoe J, Segraves R, Lucas J, Gray J. Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. Proc Natl Acad Sci U S A 1988;85:9138-42. [PMID: 2973607 DOI: 10.1073/pnas.85.23.9138] [Cited by in Crossref: 777] [Cited by in F6Publishing: 667] [Article Influence: 23.5] [Reference Citation Analysis]
245 Arnheim N. A New Approach to Constructing Genetic Maps: PCR Analysis of DNA Sequences in Individual Gametes. In: Erlich HA, editor. PCR Technology. London: Palgrave Macmillan UK; 1989. pp. 119-35. [DOI: 10.1007/978-1-349-20235-5_12] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
246 Chandler LA, Ghazi H, Jones PA, Boukamp P, Fusenig NE. Allele-specific methylation of the human c-Ha-ras-1 gene. Cell 1987;50:711-7. [PMID: 2441871 DOI: 10.1016/0092-8674(87)90329-1] [Cited by in Crossref: 50] [Cited by in F6Publishing: 53] [Article Influence: 1.5] [Reference Citation Analysis]
247 Sinnott P, Collier S, Costigan C, Dyer PA, Harris R, Strachan T. Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency. Proc Natl Acad Sci U S A 1990;87:2107-11. [PMID: 2315306 DOI: 10.1073/pnas.87.6.2107] [Cited by in Crossref: 36] [Cited by in F6Publishing: 36] [Article Influence: 1.2] [Reference Citation Analysis]
248 Cheng JM, Hiemstra JL, Schneider SS, Naumova A, Cheung NV, Cohn SL, Diller L, Sapienza C, Brodeur GM. Preferential amplification of the paternal allele of the N–myc gene in human neuroblastomas. Nat Genet 1993;4:191-4. [DOI: 10.1038/ng0693-191] [Cited by in Crossref: 43] [Cited by in F6Publishing: 37] [Article Influence: 1.5] [Reference Citation Analysis]
249 Brenig B, Brem G. Genetic Engineering Approaches to Pig Production. Reprod Domest Anim 1991;26:14-21. [DOI: 10.1111/j.1439-0531.1991.tb01506.x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
250 Odelberg S, Plaetke R, Eldridge J, Ballard L, O'connell P, Nakamura Y, Leppert M, Lalouel J, White R. Characterization of eight VNTR loci by agarose gel electrophoresis. Genomics 1989;5:915-24. [DOI: 10.1016/0888-7543(89)90134-1] [Cited by in Crossref: 62] [Cited by in F6Publishing: 30] [Article Influence: 1.9] [Reference Citation Analysis]
251 Deapen D, Escalante A, Weinrib L, Horwitz D, Bachman B, Roy-Burman P, Walker A, Mack TM. A revised estimate of twin concordance in systemic lupus erythematosus. Arthritis Rheum 1992;35:311-8. [PMID: 1536669 DOI: 10.1002/art.1780350310] [Cited by in Crossref: 516] [Cited by in F6Publishing: 425] [Article Influence: 17.8] [Reference Citation Analysis]
252 Nishikawa N, Oishi M, Kiyama R. Construction of a Human Genomic Library of Clones Containing Poly(dG-dA)•Poly(dT-dC) Tracts by Mg2+-dependent Triplex Affinity Capture. Journal of Biological Chemistry 1995;270:9258-64. [DOI: 10.1074/jbc.270.16.9258] [Cited by in Crossref: 27] [Cited by in F6Publishing: 20] [Article Influence: 1.0] [Reference Citation Analysis]
253 Duncan G, Thomas E, Gallol JC, Baird LS, Garrison J, Herrera RJ. Human phylogenetic relationships according to the D1S80 locus. Genetica 1996;98:277-87. [DOI: 10.1007/bf00057592] [Cited by in Crossref: 17] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
254 Winter P, Kahl G. Molecular marker technologies for plant improvement. World J Microbiol Biotechnol 1995;11:438-48. [PMID: 24414752 DOI: 10.1007/BF00364619] [Cited by in Crossref: 77] [Cited by in F6Publishing: 8] [Article Influence: 11.0] [Reference Citation Analysis]
255 Pena SD, Chakraborty R. Paternity testing in the DNA era. Trends Genet 1994;10:204-9. [PMID: 8073534 DOI: 10.1016/0168-9525(94)90257-7] [Cited by in Crossref: 71] [Cited by in F6Publishing: 32] [Article Influence: 2.6] [Reference Citation Analysis]
256 Silva R, Moura-neto RS. Allelic frequency distribution for three VNTR markers—D6S132, D7S467, D17S26—in Rio de Janeiro population, Brazil. Forensic Science International 1998;94:33-8. [DOI: 10.1016/s0379-0738(98)00028-0] [Cited by in Crossref: 4] [Article Influence: 0.2] [Reference Citation Analysis]
257 Park J, Han H, Kang M, Nakamura Y. Presymptomatic diagnosis of familial adenomatous polyposis coli. Diseases of the Colon & Rectum 1994;37:700-7. [DOI: 10.1007/bf02054415] [Cited by in Crossref: 13] [Article Influence: 0.5] [Reference Citation Analysis]
258 Nakamura Y, Holm T, Gillilan S, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pTHH59) on chromosome 17q [D17S4]. Nucleic Acids Res 1988;16:3598. [PMID: 2897667 DOI: 10.1093/nar/16.8.3598] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 0.2] [Reference Citation Analysis]
259 Gerdes AM, Petersen MB, Schrøder HD, Wulff K, Brøndum-nielsen K. Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10; 17) may indicate candidate gene regions. Clinical Genetics 1994;45:11-6. [DOI: 10.1111/j.1399-0004.1994.tb03982.x] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
260 Carroll PE, Okuda M, Horn HF, Biddinger P, Stambrook PJ, Gleich LL, Li YQ, Tarapore P, Fukasawa K. Centrosome hyperamplification in human cancer: chromosome instability induced by p53 mutation and/or Mdm2 overexpression. Oncogene 1999;18:1935-44. [PMID: 10208415 DOI: 10.1038/sj.onc.1202515] [Cited by in Crossref: 177] [Cited by in F6Publishing: 169] [Article Influence: 8.0] [Reference Citation Analysis]
261 Weiss ML, Wilson V, Chan C, Turner T, Jeffreys AJ. Application of DNA fingerprinting probes to old world monkeys. Am J Primatol 1988;16:73-9. [DOI: 10.1002/ajp.1350160109] [Cited by in Crossref: 23] [Cited by in F6Publishing: 11] [Article Influence: 0.7] [Reference Citation Analysis]
262 Bitan M, Or R, Shapira MY, Resnick IB, Gesundheit B, Ackerstein A, Samuel S, Elad S, Slavin S. Time to engraftment following allogeneic stem cell transplantation is significantly longer in patients with myelodysplastic syndrome than with acute myeloid leukemia. Bone Marrow Transplant 2008;41:69-78. [DOI: 10.1038/sj.bmt.1705878] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
263 Song JM, Mobley J, Vo-dinh T. Integrated circuit microchip system with multiplex capillary electrophoresis module for DNA analysis. Analytica Chimica Acta 2002;466:187-92. [DOI: 10.1016/s0003-2670(02)00552-4] [Cited by in Crossref: 7] [Article Influence: 0.4] [Reference Citation Analysis]
264 Tokino T, Imai T, Tanigami A, Takiguchi S, Nakamura Y. Physical mapping of a 950-kb region surrounding a locus (D10S102) tightly linked to the MEN2A gene. Genomics 1992;12:394-400. [DOI: 10.1016/0888-7543(92)90390-e] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
265 Jeffreys AJ, Neumann R, Wilson V. Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis. Cell 1990;60:473-85. [PMID: 2406022 DOI: 10.1016/0092-8674(90)90598-9] [Cited by in Crossref: 290] [Cited by in F6Publishing: 233] [Article Influence: 9.4] [Reference Citation Analysis]
266 Jena RC, Chand PK. Multiple DNA marker-assisted diversity analysis of Indian mango (Mangifera indica L.) populations. Sci Rep 2021;11:10345. [PMID: 33990638 DOI: 10.1038/s41598-021-89470-3] [Reference Citation Analysis]
267 Brenner JC, Graham MP, Kumar B, Saunders LM, Kupfer R, Lyons RH, Bradford CR, Carey TE. Genotyping of 73 UM-SCC head and neck squamous cell carcinoma cell lines. Head Neck 2010;32:417-26. [PMID: 19760794 DOI: 10.1002/hed.21198] [Cited by in Crossref: 44] [Cited by in F6Publishing: 155] [Article Influence: 4.0] [Reference Citation Analysis]
268 Woo PC, Lau SK, Yip CC, Huang Y, Tsoi HW, Chan KH, Yuen KY. Comparative analysis of 22 coronavirus HKU1 genomes reveals a novel genotype and evidence of natural recombination in coronavirus HKU1. J Virol 2006;80:7136-45. [PMID: 16809319 DOI: 10.1128/JVI.00509-06] [Cited by in Crossref: 141] [Cited by in F6Publishing: 109] [Article Influence: 9.4] [Reference Citation Analysis]
269 Dixon LK, Bristow C, Wilkinson PJ, Sumption KJ. Identification of a variable region of the African swine fever virus genome that has undergone separate DNA rearrangements leading to expansion of minisatellite-like sequences. Journal of Molecular Biology 1990;216:677-88. [DOI: 10.1016/0022-2836(90)90391-x] [Cited by in Crossref: 13] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
270 Harada Y, Katagiri T, Ito I, Nakamura Y, Emi M, Akiyama F, Sakamoto G, Kasumi F. Genetic studies of 457 breast cancers. Clinicopathologic parameters compared with genetic alterations. Cancer 1994;74:2281-6. [DOI: 10.1002/1097-0142(19941015)74:8<2281::aid-cncr2820740812>3.0.co;2-i] [Cited by in Crossref: 47] [Cited by in F6Publishing: 10] [Article Influence: 1.7] [Reference Citation Analysis]
271 Sadowsky MJ, Call DR, Santo Domingo JW. The Future of Microbial Source Tracking Studies. In: Santo Domingo JW, Sadowsky MJ, Doyle MP, editors. Microbial Source Tracking. Washington: ASM Press; 2006. pp. 235-77. [DOI: 10.1128/9781555815769.ch8] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 1.1] [Reference Citation Analysis]
272 Chakraborty R, Deka R, Jin L, Ferrell RE. Allele sharing at six VNTR loci and genetic distances among three ethnically defined human populations. Am J Hum Biol 1992;4:387-97. [DOI: 10.1002/ajhb.1310040315] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 0.4] [Reference Citation Analysis]
273 Franco B, Lai LW, Patterson D, Ledbetter DH, Trask BJ, van den Engh G, Iannaccone S, Frances S, Patel PI, Lupski JR. Molecular characterization of a patient with del(1)(q23-q25). Hum Genet 1991;87:269-77. [PMID: 1677922 DOI: 10.1007/BF00200903] [Cited by in Crossref: 20] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
274 Alvarez-Cubero MJ, Saiz M, Martinez-Gonzalez LJ, Alvarez JC, Eisenberg AJ, Budowle B, Lorente JA. Genetic identification of missing persons: DNA analysis of human remains and compromised samples. Pathobiology 2012;79:228-38. [PMID: 22722562 DOI: 10.1159/000334982] [Cited by in Crossref: 33] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
275 Coon H, Jensen S, Holik J, Hoff M, Myles-worsley M, Reimherr F, Wender P, Waldo M, Freedman R, Leppert M, Byerley W. Genomic scan for genes predisposing to schizophrenia. Am J Med Genet 1994;54:59-71. [DOI: 10.1002/ajmg.1320540111] [Cited by in Crossref: 130] [Cited by in F6Publishing: 123] [Article Influence: 4.8] [Reference Citation Analysis]
276 Romano-spica V, Vijg J. Two-dimensional DNA electrophoresis: state of the art and applications. Elsevier; 1997. pp. 1-30. [DOI: 10.1016/s1387-2656(08)70028-0] [Cited by in Crossref: 2] [Article Influence: 0.1] [Reference Citation Analysis]
277 Lin Z, Ohshima T, Gao S, Kondo T, Takayasu T, Sato Y, Sun K. Genetic variation and relationships at five STR loci in five distinct ethnic groups in China. Forensic Science International 2000;112:179-89. [DOI: 10.1016/s0379-0738(00)00272-3] [Cited by in Crossref: 8] [Article Influence: 0.4] [Reference Citation Analysis]
278 Jeffreys AJ, Royle NJ, Patel I, Armour JAL, Macleod A, Collick A, Gray IC, Neumann R, Gibbs M, Crosier M, Hill M, Signer E, Monckton D. Principles and Recent Advances in Human DNA Fingerprinting. In: Burke T, Dolf G, Jeffreys AJ, Wolff R, editors. DNA Fingerprinting: Approaches and Applications. Basel: Birkhäuser; 1991. pp. 1-19. [DOI: 10.1007/978-3-0348-7312-3_1] [Cited by in Crossref: 19] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
279 Park LK, Moran P. Developments in molecular genetic techniques in fisheries. Rev Fish Biol Fisheries 1994;4:272-99. [DOI: 10.1007/bf00042906] [Cited by in Crossref: 58] [Article Influence: 2.1] [Reference Citation Analysis]
280 Kidd KK, Pakstis AJ, Speed WC, Kidd JR. Understanding Human DNA Sequence Variation. Journal of Heredity 2004;95:406-20. [DOI: 10.1093/jhered/esh060] [Cited by in Crossref: 52] [Cited by in F6Publishing: 39] [Article Influence: 3.1] [Reference Citation Analysis]
281 Herman GE, Berry M, Munro E, Craig IW, Levy ER. The construction of human somatic cell hybrids containing portions of the mouse X chromosome and their use to generate DNA probes via interspersed repetitive sequence polymerase chain reaction. Genomics 1991;10:961-70. [DOI: 10.1016/0888-7543(91)90186-i] [Cited by in Crossref: 15] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
282 O'brien SJ. Mammalian genome mapping: lessons and prospects. Current Opinion in Genetics & Development 1991;1:105-11. [DOI: 10.1016/0959-437x(91)80050-v] [Cited by in Crossref: 80] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
283 Giacalone J, Friedes J, Francke U. A novel GC-rich human macrosatellite VNTR in Xq24 is differentially methylated on active and inactive X chromosomes. Nat Genet 1992;1:137-43. [PMID: 1302007 DOI: 10.1038/ng0592-137] [Cited by in Crossref: 59] [Cited by in F6Publishing: 52] [Article Influence: 2.1] [Reference Citation Analysis]
284 Cornélis F, Hashimoto L, Loveridge J, MacCarthy A, Buckle V, Julier C, Bell J. Identification of a CA repeat at the TCRA locus using yeast artificial chromosomes: a general method for generating highly polymorphic markers at chosen loci. Genomics 1992;13:820-5. [PMID: 1386339 DOI: 10.1016/0888-7543(92)90159-p] [Cited by in Crossref: 26] [Cited by in F6Publishing: 5] [Article Influence: 0.9] [Reference Citation Analysis]
285 Jin L, Chakraborty R. Population dynamics of DNA fingerprint patterns within and between populations. Genet Res 1994;63:1-9. [DOI: 10.1017/s001667230003202x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
286 Nellemann LJ, Møller A, Morling N. PCR typing of DNA fragments of the short tandem repeat (STR) system HUMTH01 in Danes and Greenland Eskimos. Forensic Sci Int 1994;68:45-51. [PMID: 7959480 DOI: 10.1016/0379-0738(94)90378-6] [Cited by in Crossref: 15] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
287 Clarke TH, Gomez A, Singh H, Nelson KE, Brinkac LM. Integrating the microbiome as a resource in the forensics toolkit. Forensic Science International: Genetics 2017;30:141-7. [DOI: 10.1016/j.fsigen.2017.06.008] [Cited by in Crossref: 40] [Cited by in F6Publishing: 27] [Article Influence: 10.0] [Reference Citation Analysis]
288 Tian S, Luo LC, Ge S, Zhang ZY. Clear genetic structure of Pinus kwangtungensis (Pinaceae) revealed by a plastid DNA fragment with a novel minisatellite. Ann Bot 2008;102:69-78. [PMID: 18463112 DOI: 10.1093/aob/mcn068] [Cited by in Crossref: 29] [Cited by in F6Publishing: 14] [Article Influence: 2.2] [Reference Citation Analysis]
289 Madreperla SA, Bookstein R, Jones OW, Lee WH. Retinoblastoma cell lines Y79, RB355 and WERI-Rb27 are genetically related. Ophthalmic Paediatr Genet 1991;12:49-56. [PMID: 1679230 DOI: 10.3109/13816819109023085] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 0.3] [Reference Citation Analysis]
290 Park S, Kang Y, Kim B, Lee S, Lee E, Lee K, Park K, Lee J. Loss of heterozygosity on the short arm of chromosome 17 in uterine cervical carcinomas. Cancer Genetics and Cytogenetics 1995;79:74-8. [DOI: 10.1016/0165-4608(94)00103-i] [Cited by in Crossref: 16] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
291 Ames D, Murphy N, Helentjaris T, Sun N, Chandler V. Comparative analyses of human single- and multilocus tandem repeats. Genetics 2008;179:1693-704. [PMID: 18562644 DOI: 10.1534/genetics.108.087882] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 1.2] [Reference Citation Analysis]
292 Paul P, Jagelman DG, Fazio VW, Mcgannon E. Evaluation of polymorphic genetic markers for linkage to the familial adenomatous polyposis locus on chromosome 5. Diseases of the Colon & Rectum 1990;33:740-4. [DOI: 10.1007/bf02052318] [Cited by in Crossref: 2] [Article Influence: 0.1] [Reference Citation Analysis]
293 Nagler A, Or R, Naparstek E, Varadi G, Slavin S. Second allogeneic stem cell transplantation using nonmyeloablative conditioning for patients who relapsed or developed secondary malignancies following autologous transplantation. Experimental Hematology 2000;28:1096-104. [DOI: 10.1016/s0301-472x(00)00511-7] [Cited by in Crossref: 56] [Cited by in F6Publishing: 6] [Article Influence: 2.7] [Reference Citation Analysis]
294 Nakamura Y, Holm T, White R. Isolation and mapping of a polymorphic DNA sequence (pTHH33) on chromosome 1q [D1S81]. Nucleic Acids Res 1988;16:9363. [PMID: 2902590 DOI: 10.1093/nar/16.19.9363] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.1] [Reference Citation Analysis]
295 White R, Nakamura Y, O'Connell P, Leppert M, Lalouel JM, Barker D, Goldgar D, Skolnick M, Carey J, Wallis CE. Tightly linked markers for the neurofibromatosis type 1 gene. Genomics 1987;1:364-7. [PMID: 2896632 DOI: 10.1016/0888-7543(87)90040-1] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 0.5] [Reference Citation Analysis]
296 Desmarais E, Vigneron S, Buresi C, Cambien F, Cambou JP, Roizes G. Variant mapping of the Apo(B) AT rich minisatellite. Dependence on nucleotide sequence of the copy number variations. Instability of the non-canonical alleles. Nucleic Acids Res 1993;21:2179-84. [PMID: 8502559 DOI: 10.1093/nar/21.9.2179] [Cited by in Crossref: 18] [Cited by in F6Publishing: 11] [Article Influence: 0.6] [Reference Citation Analysis]
297 Estivill X, Armengol L. Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies. PLoS Genet 2007;3:1787-99. [PMID: 17953491 DOI: 10.1371/journal.pgen.0030190] [Cited by in Crossref: 140] [Cited by in F6Publishing: 114] [Article Influence: 10.0] [Reference Citation Analysis]
298 Mowery-rushton PA, Driscoll DJ, Nicholls RD, Locker J, Surti U. DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region. Am J Med Genet 1996;61:140-6. [DOI: 10.1002/(sici)1096-8628(19960111)61:2<140::aid-ajmg7>3.0.co;2-0] [Cited by in Crossref: 14] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
299 Fukuda M, Viitala J, Matteson J, Carlsson SR. Cloning of cDNAs encoding human lysosomal membrane glycoproteins, h-lamp-1 and h-lamp-2. Comparison of their deduced amino acid sequences. Journal of Biological Chemistry 1988;263:18920-8. [DOI: 10.1016/s0021-9258(18)37370-8] [Cited by in Crossref: 108] [Article Influence: 3.3] [Reference Citation Analysis]
300 Goddard KA, Wijsman EM. Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers. Genet Epidemiol 2002;22:205-20. [PMID: 11921081 DOI: 10.1002/gepi.0177] [Cited by in Crossref: 21] [Cited by in F6Publishing: 16] [Article Influence: 1.1] [Reference Citation Analysis]
301 Haberfeld A, Kalay D, Weisberger P, Gal O, Hilliel J. Application of Multilocus Molecular Markers in Cattle Breeding. 1. Minisatellites and Microsatellites. Journal of Dairy Science 1993;76:645-52. [DOI: 10.3168/jds.s0022-0302(93)77386-5] [Cited by in Crossref: 4] [Article Influence: 0.1] [Reference Citation Analysis]
302 Shen N, Li Z, Waye JS, Francis G, Chang PL. Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiency. Am J Med Genet 1993;45:631-7. [DOI: 10.1002/ajmg.1320450523] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 0.6] [Reference Citation Analysis]
303 Sun R, Spain TA, Lin SF, Miller G. Sp1 binds to the precise locus of end processing within the terminal repeats of Epstein-Barr virus DNA. J Virol 1997;71:6136-43. [DOI: 10.1128/jvi.71.8.6136-6143.1997] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 0.5] [Reference Citation Analysis]
304 Yumoto Y, Hanafusa T, Hada H, Morita T, Ooguchi S, Shinji N, Mitani T, Hamaya K, Koide N, Tsuji T. Loss of heterozygosity and analysis of mutation of p53 in hepatocellular carcinoma. J Gastroenterol Hepatol. 1995;10:179-185. [PMID: 7540433 DOI: 10.1111/j.1440-1746.1995.tb01075.x] [Cited by in Crossref: 53] [Cited by in F6Publishing: 48] [Article Influence: 2.0] [Reference Citation Analysis]
305 Barros P, Blanco MG, Boán F, Gómez-márquez J. Heteroduplex analysis of minisatellite variability. Electrophoresis 2005;26:4304-9. [DOI: 10.1002/elps.200500296] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
306 Dheer P, Rautela I, Sharma V, Dhiman M, Sharma A, Sharma N, Sharma MD. Evolution in crop improvement approaches and future prospects of molecular markers to CRISPR/Cas9 system. Gene 2020;753:144795. [PMID: 32450202 DOI: 10.1016/j.gene.2020.144795] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
307 Nakagama H, Kaneko S, Shima H, Inamori H, Fukuda H, Kominami R, Sugimura T, Nagao M. Induction of minisatellite mutation in NIH 3T3 cells by treatment with the tumor promoter okadaic acid. Proc Natl Acad Sci U S A 1997;94:10813-6. [PMID: 9380716 DOI: 10.1073/pnas.94.20.10813] [Cited by in Crossref: 42] [Cited by in F6Publishing: 33] [Article Influence: 1.8] [Reference Citation Analysis]
308 Schaal BA, O'kane SL, Rogstad SH. DNA variation in plant populations. Trends in Ecology & Evolution 1991;6:329-33. [DOI: 10.1016/0169-5347(91)90041-u] [Cited by in Crossref: 27] [Article Influence: 0.9] [Reference Citation Analysis]
309 Leonard NJ, Bernier FP, Rudd N, Machin GA, Bamforth F, Bamforth S, Grundy P, Johnson C. Two pairs of male monozygotic twins discordant for Wiedemann-Beckwith syndrome. Am J Med Genet 1996;61:253-7. [DOI: 10.1002/(sici)1096-8628(19960122)61:3<253::aid-ajmg9>3.0.co;2-v] [Cited by in Crossref: 27] [Cited by in F6Publishing: 5] [Article Influence: 1.1] [Reference Citation Analysis]
310 Latif F, Modi WS, Duh FM, Schmidt L, Li H, Geil L, Orcutt ML, Heppell-Parton A, Rabbitts PH, Linehan WM. Molecular and genetic characterization and physical mapping of 11 new markers detecting multiallele restriction fragment length polymorphisms on the short arm of human chromosome 3. Hum Genet 1992;90:17-22. [PMID: 1358787 DOI: 10.1007/BF00210739] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
311 Danpure CJ, Birdsey GM, Rumsby G, Lumb MJ, Purdue PE, Allsop J. Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine: Glyoxylate aminotransferase gene. Hum Genet 1994;94:55-64. [DOI: 10.1007/bf02272842] [Cited by in Crossref: 26] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
312 Rosetti N, Remis MI. Spatial genetic structure and mitochondrial DNA phylogeography of Argentinean populations of the grasshopper Dichroplus elongatus. PLoS One 2012;7:e40807. [PMID: 22859953 DOI: 10.1371/journal.pone.0040807] [Cited by in Crossref: 25] [Cited by in F6Publishing: 9] [Article Influence: 2.8] [Reference Citation Analysis]
313 Korneluk R, Mackenzie A, Nakamura Y, Dubé I, Jacob P, Hunter A. A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus. Genomics 1989;5:596-604. [DOI: 10.1016/0888-7543(89)90028-1] [Cited by in Crossref: 36] [Cited by in F6Publishing: 33] [Article Influence: 1.1] [Reference Citation Analysis]
314 Nakamura Y, Ballard L, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30]. Nucleic Acids Res 1988;16:5707. [PMID: 2455284 DOI: 10.1093/nar/16.12.5707] [Cited by in Crossref: 31] [Cited by in F6Publishing: 44] [Article Influence: 0.9] [Reference Citation Analysis]
315 Carnaby S, Butcher P, Summerbell C, Naeem A, Farthing M. Minisatellites corresponding to the human polycore probes 33.6 and 33.15 in the genome of the most ‘primitive’ known eukaryote Giardia lamblia. Gene 1995;166:167-72. [DOI: 10.1016/0378-1119(95)00572-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.2] [Reference Citation Analysis]
316 Schneider P, Fimmers R, Woodroffe S, Werrett D, Bär W, Brinkmann B, Eriksen B, Jones S, Kloosterman A, Mevåg B, Pascali V, Rittner C, Schmitter H, Thomson J, Gill P. Report of a european collaborative exercise comparing DNA typing results using a single locus VNTR probe. Forensic Science International 1991;49:1-15. [DOI: 10.1016/0379-0738(91)90166-g] [Cited by in Crossref: 41] [Cited by in F6Publishing: 1] [Article Influence: 1.4] [Reference Citation Analysis]
317 Weber WW, Cronin MT. Pharmacogenetic Testing. In: Meyers RA, editor. Encyclopedia of Analytical Chemistry. Wiley; 2006. [DOI: 10.1002/9780470027318.a0537] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
318 Lathrop M, Nakamura Y, Cartwright P, O'connell P, Leppert M, Jones C, Tateishi H, Bragg T, Lalouel J, White R. A primary genetic map of markers for human chromosome 10. Genomics 1988;2:157-64. [DOI: 10.1016/0888-7543(88)90098-5] [Cited by in Crossref: 62] [Cited by in F6Publishing: 54] [Article Influence: 1.9] [Reference Citation Analysis]
319 O'reilly P, Wright JM. The evolving technology of DNA fingerprinting and its application to fisheries and aquaculture. J Fish Biology 1995;47:29-55. [DOI: 10.1111/j.1095-8649.1995.tb06042.x] [Cited by in Crossref: 104] [Cited by in F6Publishing: 38] [Article Influence: 4.0] [Reference Citation Analysis]
320 Coleman MG, Gough AC, Bunyan DJ, Braham D, Eccles DM, Primrose JN. Minisatellite instability is found in colorectal tumours with mismatch repair deficiency. Br J Cancer 2001;85:1486-91. [PMID: 11720433 DOI: 10.1054/bjoc.2001.2058] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
321 Hayward N, Chen P, Nancarrow D, Kearsley J, Smith P, Kidson C, Ellem K. Detection of somatic mutations in tumours of diverse types by DNA fingerprinting with M13 phage DNA. Int J Cancer 1990;45:687-90. [DOI: 10.1002/ijc.2910450420] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 0.3] [Reference Citation Analysis]
322 Allingham-hawkins DJ, Tomkins DJ. Somatic cell hybridization of roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes. Somat Cell Mol Genet 1991;17:455-62. [DOI: 10.1007/bf01233169] [Cited by in Crossref: 7] [Article Influence: 0.2] [Reference Citation Analysis]
323 Kobayashi E, Ikadai H, Imamichi T, Kunieda T. A polymorphism detected in a variable number of tandem repeats (VNTR) of the seminal vesicle secretion (SVS) IV gene in inbred rats. Biochem Genet 1992;30:339-46. [PMID: 1445179 DOI: 10.1007/BF00569324] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
324 Caetano-anollés G, Bassam BJ, Gresshoff PM. DNA amplification fingerprinting: A strategy for genome analysis. Plant Mol Biol Rep 1991;9:294-307. [DOI: 10.1007/bf02672006] [Cited by in Crossref: 64] [Article Influence: 2.1] [Reference Citation Analysis]
325 Luhm RA, Bellissimo DB, Uzgiris AJ, Drobyski WR, Hessner MJ. Quantitative evaluation of post-bone marrow transplant engraftment status using fluorescent-labeled variable number of tandem repeats. Mol Diagn 2000;5:129-38. [PMID: 11066014 DOI: 10.1007/BF03262031] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
326 Nagler A, Aker M, Or R, Naparstek E, Varadi G, Brautbar C, Slavin S. Low-intensity conditioning is sufficient to ensure engraftment in matched unrelated bone marrow transplantation. Exp Hematol 2001;29:362-70. [PMID: 11274765 DOI: 10.1016/s0301-472x(00)00655-x] [Cited by in Crossref: 82] [Cited by in F6Publishing: 9] [Article Influence: 4.1] [Reference Citation Analysis]
327 Rappold GA, Henke A, Pohlschmid M, Huisman THJ. Pseudoautosomal repeat displays higher variability in Blacks than in Caucasians. Hum Genet 1992;88:573-8. [DOI: 10.1007/bf00219347] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
328 Baba Y. Analysis of disease-causing genes and DNA-based drugs by capillary electrophoresis towards DNA diagnosis and gene therapy for human diseases. Journal of Chromatography B: Biomedical Sciences and Applications 1996;687:271-302. [DOI: 10.1016/s0378-4347(96)00262-9] [Cited by in Crossref: 56] [Article Influence: 2.2] [Reference Citation Analysis]
329 Beckmann JS, Soller M. Detection of linkage between marker loci and loci affecting quantitative traits in crosses between segregating populations. Theoret Appl Genetics 1988;76:228-36. [DOI: 10.1007/bf00257850] [Cited by in Crossref: 54] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
330 Brooks JD, Bova GS, Marshall FF, Isaacs WB. Tumor Suppressor Gene Allelic Loss in Human Renal Cancers. Journal of Urology 1993;150:1278-83. [DOI: 10.1016/s0022-5347(17)35760-9] [Cited by in Crossref: 37] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
331 Fraser NJ, Boyd Y, Craig I. Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22. Genomics 1989;5:144-8. [DOI: 10.1016/0888-7543(89)90099-2] [Cited by in Crossref: 52] [Cited by in F6Publishing: 51] [Article Influence: 1.6] [Reference Citation Analysis]
332 Queller DC, Goodnight KF. ESTIMATING RELATEDNESS USING GENETIC MARKERS. Evolution 1989;43:258-75. [DOI: 10.1111/j.1558-5646.1989.tb04226.x] [Cited by in Crossref: 1233] [Cited by in F6Publishing: 754] [Article Influence: 308.3] [Reference Citation Analysis]
333 Righetti PG, Gelfi C. Capillary electrophoresis of DNA for molecular diagnostics. Electrophoresis 1997;18:1709-14. [DOI: 10.1002/elps.1150181003] [Cited by in Crossref: 32] [Cited by in F6Publishing: 24] [Article Influence: 1.3] [Reference Citation Analysis]
334 Edwards A, Hammond HA, Jin L, Caskey CT, Chakraborty R. Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics 1992;12:241-53. [PMID: 1740333 DOI: 10.1016/0888-7543(92)90371-x] [Cited by in Crossref: 924] [Cited by in F6Publishing: 122] [Article Influence: 31.9] [Reference Citation Analysis]
335 Sauer S, Kliem M. Mass spectrometry tools for the classification and identification of bacteria. Nat Rev Microbiol 2010;8:74-82. [PMID: 20010952 DOI: 10.1038/nrmicro2243] [Cited by in Crossref: 309] [Cited by in F6Publishing: 204] [Article Influence: 28.1] [Reference Citation Analysis]
336 Richard GF, Kerrest A, Dujon B. Comparative genomics and molecular dynamics of DNA repeats in eukaryotes. Microbiol Mol Biol Rev 2008;72:686-727. [PMID: 19052325 DOI: 10.1128/MMBR.00011-08] [Cited by in Crossref: 343] [Cited by in F6Publishing: 151] [Article Influence: 28.6] [Reference Citation Analysis]
337 Hoffman JD, Ward K. Genetic Factors in Preterm Delivery: . Obstetrical & Gynecological Survey 1999;54:203-10. [DOI: 10.1097/00006254-199903000-00025] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 0.8] [Reference Citation Analysis]
338 Putze J, Hennequin C, Nougayrède JP, Zhang W, Homburg S, Karch H, Bringer MA, Fayolle C, Carniel E, Rabsch W. Genetic structure and distribution of the colibactin genomic island among members of the family Enterobacteriaceae. Infect Immun. 2009;77:4696-4703. [PMID: 19720753 DOI: 10.1128/iai.00522-09] [Cited by in Crossref: 182] [Cited by in F6Publishing: 96] [Article Influence: 15.2] [Reference Citation Analysis]
339 Gyllensten UB, Jakobsson S, Temrin H. No evidence for illegitimate young in monogamous and polygynous warblers. Nature 1990;343:168-70. [DOI: 10.1038/343168a0] [Cited by in Crossref: 89] [Cited by in F6Publishing: 44] [Article Influence: 2.9] [Reference Citation Analysis]
340 Chen C, Guo Y, Jin X, Cui W, Wei Y, Fang Y, Lan Q, Kong T, Xie T, Zhu B. Forensic characteristics and population genetics of Chinese Kazakh ethnic minority with an efficient STR panel. PeerJ 2019;7:e6802. [PMID: 31086740 DOI: 10.7717/peerj.6802] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
341 Bustamante AV, Sanso AM, Segura DO, Parma AE, Lucchesi PM. Dynamic of mutational events in variable number tandem repeats of Escherichia coli O157:H7. Biomed Res Int 2013;2013:390354. [PMID: 24093095 DOI: 10.1155/2013/390354] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
342 Neuman WL, Wasylyshyn ML, Jacoby R, Erroi F, Angriman I, Montag A, Brasitus T, Michelassi F, Westbrook CA. Evidence for a common molecular pathogenesis in colorectal, gastric, and pancreatic cancer. Genes Chromosomes Cancer. 1991;3:468-473. [PMID: 1663781 DOI: 10.1002/gcc.2870030609] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 1.1] [Reference Citation Analysis]
343 Jarman AP, Wells RA. Hypervariable minisatellites: recombinators or innocent bystanders? Trends in Genetics 1989;5:367-71. [DOI: 10.1016/0168-9525(89)90171-6] [Cited by in Crossref: 84] [Cited by in F6Publishing: 58] [Article Influence: 2.6] [Reference Citation Analysis]
344 Sperber GH, Machin GA, Bamforth FJ. Mirror-image dental fusion and discordance in monozygotic twins. Am J Med Genet 1994;51:41-5. [DOI: 10.1002/ajmg.1320510110] [Cited by in Crossref: 36] [Cited by in F6Publishing: 17] [Article Influence: 1.3] [Reference Citation Analysis]
345 Nakamura Y, Cowen J, Martin C, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pJCZ30) on chromosome 6 [D6S37]. Nucleic Acids Res 1988;16:4743. [PMID: 2898129 DOI: 10.1093/nar/16.10.4743] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
346 Crawford MH, Williams JT, Duggirala R. Genetic structure of the indigenous populations of Siberia. Am J Phys Anthropol 1997;104:177-92. [DOI: 10.1002/(sici)1096-8644(199710)104:2<177::aid-ajpa4>3.0.co;2-w] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
347 Wallace AM, Sandford AJ. Genetic Polymorphisms of Matrix Metalloproteinases: Functional Importance in the Development of Chronic Obstructive Pulmonary Disease? American Journal of PharmacoGenomics 2002;2:167-75. [DOI: 10.2165/00129785-200202030-00002] [Cited by in Crossref: 25] [Cited by in F6Publishing: 18] [Article Influence: 1.3] [Reference Citation Analysis]
348 Strauss BH, MacLeod DC, de Feyter PJ, van Suylen RJ, Uitterlinden AG, de Leeuw WJ, van Trommelen GJ, Serruys PW. Analysis of VNTR loci amplified by the polymerase chain reaction for investigating the origin of intimal smooth muscle cells in a coronary artery lesion developing after heart transplantation in man. Am Heart J 1993;125:1176-80. [PMID: 8465751 DOI: 10.1016/0002-8703(93)90137-x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
349 Rumore JL, Tschetter L, Nadon C. The Impact of Multilocus Variable-Number Tandem-Repeat Analysis on PulseNet Canada Escherichia coli O157:H7 Laboratory Surveillance and Outbreak Support, 2008-2012. Foodborne Pathog Dis 2016;13:255-61. [PMID: 26990274 DOI: 10.1089/fpd.2015.2066] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.4] [Reference Citation Analysis]
350 Mays PK, Tromp G, Kuivaniemi H, Ryynänen M, Prockop DJ. A 15 base-pair AT-Rich Variable Number Tandem Repeat in the Type III Procollagen Gene (COL3A1) as an Informative Marker for 2q31-2q32.3. Matrix 1992;12:44-9. [DOI: 10.1016/s0934-8832(11)80103-4] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
351 Bid HK, Kumar A, Mishra PK, Mittal RD. Study of interleukin-1 receptor antagonist (IL-1Ra) gene polymorphism in healthy individuals from Northern India. Indian J Clin Biochem 2004;19:119-23. [PMID: 23105468 DOI: 10.1007/BF02894269] [Cited by in Crossref: 6] [Article Influence: 0.7] [Reference Citation Analysis]
352 Boán F, González AI, Rodríguez JM, Gómez-Márquez J. Molecular characterization of a new human minisatellite that is able to form single-stranded loops in vitro and is recognized by nuclear proteins. FEBS Lett 1997;418:251-7. [PMID: 9428723 DOI: 10.1016/s0014-5793(97)01389-6] [Cited by in Crossref: 9] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
353 Takahashi E, Koyama K, Hitomi A, Nakamura Y. A high-resolution cytogenetic map of human chromosome 12: localization of 195 new cosmid markers by direct R-banding fluorescence in situ hybridization. Hum Genet 1993;92:405-9. [PMID: 8225322 DOI: 10.1007/BF01247345] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
354 Watanabe K, Nagai M, Wakai S, Arai T, Kawashima K. Loss of constitutional heterozygosity in chromosome 10 in human glioblastoma. Acta Neuropathol 1990;80:251-4. [PMID: 1975968 DOI: 10.1007/BF00294641] [Cited by in Crossref: 31] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
355 Levinson G, Gutman GA. High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. Nucleic Acids Res 1987;15:5323-38. [PMID: 3299269 DOI: 10.1093/nar/15.13.5323] [Cited by in Crossref: 243] [Cited by in F6Publishing: 206] [Article Influence: 7.1] [Reference Citation Analysis]
356 Dover GA. DNA fingerprints: Victims or perpetrators of DNA turnover? Nature 1989;342:347-8. [PMID: 2586607 DOI: 10.1038/342347a0] [Cited by in Crossref: 21] [Cited by in F6Publishing: 11] [Article Influence: 0.7] [Reference Citation Analysis]
357 Salem A, Ray D, Batzer M. Identity by descent and DNA sequence variation of human SINE and LINE elements. Cytogenet Genome Res 2004;108:63-72. [DOI: 10.1159/000080803] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 1.3] [Reference Citation Analysis]
358 Gottlieb J, Muzyczka N. Substrate specificity of HeLa endonuclease R. A G-specific mammalian endonuclease. Journal of Biological Chemistry 1990;265:10842-50. [DOI: 10.1016/s0021-9258(19)38523-0] [Cited by in Crossref: 5] [Article Influence: 0.2] [Reference Citation Analysis]
359 Nicol Keith W, Brown R, Tan KB. Amplification of the topoisomerase ii α gene in a non-small cell lung cancer cell line and characterisation of polymorphisms at the human topoisomerase ii α and β loci in normal tissue. Genes Chromosom Cancer 1992;4:169-75. [DOI: 10.1002/gcc.2870040211] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 0.6] [Reference Citation Analysis]
360 Monteiro C, Marcelino LA, Conde AR, Saraiva C, Giphart-Gassler M, De Nooij-van Dalen AG, Van Buuren-van Seggelen V, Van der Keur M, May CA, Cole J, Lehmann AR, Steinsgrimsdottir H, Beare D, Capulas E, Armour JA. Molecular methods for the detection of mutations. Teratog Carcinog Mutagen 2000;20:357-86. [PMID: 11074520 DOI: 10.1002/1520-6866(2000)20:6<357::aid-tcm5>3.0.co;2-g] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
361 Lagoda P, Seitz G, Epplen J, Issinger O. Increased detectability of somatic changes in the DNA from human tumours after probing with ?synthetic? and ?genome-derived? hypervariable multilocus probes. Hum Genet 1989;84:35-40. [DOI: 10.1007/bf00210667] [Cited by in Crossref: 37] [Cited by in F6Publishing: 2] [Article Influence: 1.2] [Reference Citation Analysis]
362 Kolpakov R, Bana G, Kucherov G. mreps: Efficient and flexible detection of tandem repeats in DNA. Nucleic Acids Res 2003;31:3672-8. [PMID: 12824391 DOI: 10.1093/nar/gkg617] [Cited by in Crossref: 271] [Cited by in F6Publishing: 161] [Article Influence: 15.1] [Reference Citation Analysis]
363 Kumar S, Kumaria S, Sharma SK, Rao SR, Tandon P. Genetic diversity assessment of Jatropha curcas L. germplasm from Northeast India. Biomass and Bioenergy 2011;35:3063-70. [DOI: 10.1016/j.biombioe.2011.04.025] [Cited by in Crossref: 22] [Cited by in F6Publishing: 4] [Article Influence: 2.2] [Reference Citation Analysis]
364 Kuipers J, Vaandrager JW, Weghuis DO, Pearson PL, Scheres J, Lokhorst HM, Clevers H, Bast BJ. Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regions in myeloma cell lines. Cancer Genet Cytogenet 1999;109:99-107. [PMID: 10087940 DOI: 10.1016/s0165-4608(98)00157-5] [Cited by in Crossref: 40] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
365 Tautz D. Notes on the definition and nomenclature of tandemly repetitive DNA sequences. In: Pena SDJ, Chakraborty R, Epplen JT, Jeffreys AJ, editors. DNA Fingerprinting: State of the Science. Basel: Birkhäuser; 1993. pp. 21-8. [DOI: 10.1007/978-3-0348-8583-6_2] [Cited by in Crossref: 76] [Cited by in F6Publishing: 35] [Article Influence: 2.7] [Reference Citation Analysis]
366 Mathema B, Mediavilla J, Kreiswirth BN. Sequence analysis of the variable number tandem repeat in Staphylococcus aureus protein A gene: spa typing. Methods Mol Biol 2008;431:285-305. [PMID: 18287764 DOI: 10.1007/978-1-60327-032-8_22] [Cited by in Crossref: 7] [Cited by in F6Publishing: 30] [Article Influence: 0.5] [Reference Citation Analysis]
367 Zehnbauer B, Griffin C, Santos G, Wagner J. Comparison of molecular and cytogenetic methods in the evaluation of engraftment following allogeneic bone marrow transplantation. Cancer Genetics and Cytogenetics 1991;55:181-90. [DOI: 10.1016/0165-4608(91)90076-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
368 Venter DJ, Thomas DG. Multiple sequential molecular abnormalities in the evolution of human gliomas. Br J Cancer 1991;63:753-7. [PMID: 1674878 DOI: 10.1038/bjc.1991.168] [Cited by in Crossref: 42] [Cited by in F6Publishing: 38] [Article Influence: 1.4] [Reference Citation Analysis]
369 Tamura A, Tsuji H, Nishio H, Suzuki K. Haplotype analysis of a de novo allele at a vWF STR locus using flanking STR loci. Legal Medicine 1999;1:188-92. [DOI: 10.1016/s1344-6223(99)80036-4] [Cited by in Crossref: 2] [Article Influence: 0.1] [Reference Citation Analysis]
370 Beckmann JS, Estivill X, Antonarakis SE. Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability. Nat Rev Genet. 2007;8:639-646. [PMID: 17637735 DOI: 10.1038/nrg2149] [Cited by in Crossref: 290] [Cited by in F6Publishing: 226] [Article Influence: 20.7] [Reference Citation Analysis]
371 Bois PR. Hypermutable minisatellites, a human affair? Genomics 2003;81:349-55. [PMID: 12676558 DOI: 10.1016/s0888-7543(03)00021-1] [Cited by in Crossref: 24] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
372 Vogt P. Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code". Hum Genet 1990;84:301-36. [PMID: 2407640 DOI: 10.1007/BF00196228] [Cited by in Crossref: 63] [Cited by in F6Publishing: 49] [Article Influence: 2.0] [Reference Citation Analysis]
373 Lynch HT, Lampa SJ, Boman BM, Smyrk T, Watson P, Lynch JF, Lynch PM, Cristofaro G, Bufo P, Tauro AV, Mingazzini P, Digiulio E. Hereditary Nonpolyposis Colorectal Cancer—Lynch Syndromes I and II. Gastroenterology Clinics of North America 1988;17:679-712. [DOI: 10.1016/s0889-8553(21)00399-x] [Cited by in Crossref: 55] [Article Influence: 1.7] [Reference Citation Analysis]
374 Ei PW, Aung WW, Lee JS, Choi GE, Chang CL. Molecular Strain Typing of Mycobacterium tuberculosis: a Review of Frequently Used Methods. J Korean Med Sci 2016;31:1673-83. [PMID: 27709842 DOI: 10.3346/jkms.2016.31.11.1673] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 5.0] [Reference Citation Analysis]
375 Armour JA, Anttinen T, May CA, Vega EE, Sajantila A, Kidd JR, Kidd KK, Bertranpetit J, Pääbo S, Jeffreys AJ. Minisatellite diversity supports a recent African origin for modern humans. Nat Genet 1996;13:154-60. [DOI: 10.1038/ng0696-154] [Cited by in Crossref: 95] [Cited by in F6Publishing: 71] [Article Influence: 3.8] [Reference Citation Analysis]
376 Honma M, Kataoka E, Ohnishi K, Kikuno T, Hayashi M, Sofuni T, Mizusawa H. Detection of recombinational mutations in cultured human cells by Southern blot analysis with minisatellite DNA probes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 1993;286:165-72. [DOI: 10.1016/0027-5107(93)90180-n] [Cited by in Crossref: 11] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
377 Buetow K, Nishimura D, Green P, Nakamura Y, Jiang O, Murray J. A detailed multipoint gene map of chromosome 1q. Genomics 1990;8:13-21. [DOI: 10.1016/0888-7543(90)90220-o] [Cited by in Crossref: 11] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
378 Krane DE, Allen RW, Sawyer SA, Petrov DA, Hartl DL. Genetic differences at four DNA typing loci in Finnish, Italian, and mixed Caucasian populations. Proc Natl Acad Sci U S A 1992;89:10583-7. [PMID: 1438254 DOI: 10.1073/pnas.89.22.10583] [Cited by in Crossref: 27] [Cited by in F6Publishing: 15] [Article Influence: 0.9] [Reference Citation Analysis]
379 Brdic̆ka R, Nürnberg P. Checking of individuality by DNA profiling. Journal of Chromatography B: Biomedical Sciences and Applications 1993;618:167-79. [DOI: 10.1016/0378-4347(93)80033-z] [Cited by in Crossref: 4] [Article Influence: 0.1] [Reference Citation Analysis]
380 Righetti PG, Gelfi C. Analysis of clinically relevant, diagnostic DNA by capillary zone and double-gradient gel slab electrophoresis. Journal of Chromatography A 1998;806:97-112. [DOI: 10.1016/s0021-9673(97)00304-x] [Cited by in Crossref: 14] [Article Influence: 0.6] [Reference Citation Analysis]
381 Edwards M, Allen RW. Characteristics of mutations at the D5S818 locus studied with a tightly linked marker. Transfusion 2004;44:83-90. [PMID: 14692972 DOI: 10.1111/j.0041-1132.2004.00621.x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
382 Chow-Shaffer E, Sina B, Hawley WA, De Benedictis J, Scott TW. Laboratory and field evaluation of polymerase chain reaction-based forensic DNA profiling for use in identification of human blood meal sources of Aedes aegypti (Diptera: Culicidae). J Med Entomol 2000;37:492-502. [PMID: 10916289 DOI: 10.1603/0022-2585-37.4.492] [Cited by in Crossref: 46] [Cited by in F6Publishing: 31] [Article Influence: 2.2] [Reference Citation Analysis]
383 Kelly R, Bulfield G, Collick A, Gibbs M, Jeffreys AJ. Characterization of a highly unstable mouse minisatellite locus: Evidence for somatic mutation during early development. Genomics 1989;5:844-56. [DOI: 10.1016/0888-7543(89)90126-2] [Cited by in Crossref: 143] [Cited by in F6Publishing: 123] [Article Influence: 4.5] [Reference Citation Analysis]
384 Shapira MY, Resnick IB, Bitan M, Ackerstein A, Tsirigotis P, Gesundheit B, Zilberman I, Miron S, Leubovic A, Slavin S, Or R. Rapid response to alefacept given to patients with steroid resistant or steroid dependent acute graft-versus-host disease: a preliminary report. Bone Marrow Transplant 2005;36:1097-101. [DOI: 10.1038/sj.bmt.1705185] [Cited by in Crossref: 34] [Cited by in F6Publishing: 23] [Article Influence: 2.1] [Reference Citation Analysis]
385 Skolnick M, Ponder B, Seizinger B. Linkage of NF1 to 12 chromosome 17 markers: A summary of eight concurrent reports. Genomics 1987;1:382-3. [DOI: 10.1016/0888-7543(87)90043-7] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 0.4] [Reference Citation Analysis]
386 Imamura T, Arima T, Kato H, Miyamoto S, Sasazuki T, Wake N. Chromosomal deletions and K-ras gene mutations in human endometrial carcinomas. Int J Cancer 1992;51:47-52. [DOI: 10.1002/ijc.2910510110] [Cited by in Crossref: 53] [Cited by in F6Publishing: 51] [Article Influence: 1.8] [Reference Citation Analysis]
387 Nakamura Y, Culver M, Gill J, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence pMLJ14 on chromosome 14 [D14S13]. Nucleic Acids Res 1988;16:381. [PMID: 2893345 DOI: 10.1093/nar/16.1.381] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
388 Zhao QZ, Liang XL, Mitra S, Gourdon G, Alter BP. Cloning and characterization of the mouse alpha globin cluster and a new hypervariable marker. Mammalian Genome 1996;7:749-53. [DOI: 10.1007/s003359900225] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
389 Rogers J, Ruano G, Kidd KK. Variability in nuclear DNA among nonhuman primates: Application of molecular genetic techniques to intra- and inter-species genetic analyses. Am J Primatol 1992;27:93-105. [DOI: 10.1002/ajp.1350270205] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
390 Verma SK, Singh L. Novel universal primers establish identity of an enormous number of animal species for forensic application: PRIMER NOTE. Molecular Ecology Notes 2003;3:28-31. [DOI: 10.1046/j.1471-8286.2003.00340.x] [Cited by in Crossref: 140] [Cited by in F6Publishing: 48] [Article Influence: 7.4] [Reference Citation Analysis]
391 Dansey RD, Baynes RD. Nonablative allogeneic hematopoietic stem cell transplantation: . Current Opinion in Oncology 2001;13:27-32. [DOI: 10.1097/00001622-200101000-00006] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
392 Sato Y, Mitomi K, Sunami T, Kondo J, Takénaka A. DNA octaplex formation with an I-motif of water-mediated A-quartets: reinterpretation of the crystal structure of d(GCGAAAGC). J Biochem 2006;140:759-62. [PMID: 17062599 DOI: 10.1093/jb/mvj213] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
393 Emi M, Takahashi E, Koyama K, Okui K, Oshimura M, Nakamura Y. Isolation and mapping of 88 new RFLP markers on human chromosome 8. Genomics 1992;13:1261-6. [DOI: 10.1016/0888-7543(92)90044-s] [Cited by in Crossref: 15] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
394 Renges H, Peacock K, Dunning AM, Talmud P, Humphries SE. Genetic relationship between the 3?-VNTR and diallelic apolipoprotein B gene polymorphisms: Haplotype analysis in individuals of European and South Asian origin. Ann Human Genet 1992;56:11-33. [DOI: 10.1111/j.1469-1809.1992.tb01126.x] [Cited by in Crossref: 37] [Cited by in F6Publishing: 26] [Article Influence: 1.3] [Reference Citation Analysis]
395 Jeffreys AJ, Royle NJ, Wilson V, Wong Z. Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. Nature 1988;332:278-81. [PMID: 3347271 DOI: 10.1038/332278a0] [Cited by in Crossref: 481] [Cited by in F6Publishing: 376] [Article Influence: 14.6] [Reference Citation Analysis]
396 Cropp CS. Mutations in breast cancer. Cancer Letters 1995;90:51-6. [DOI: 10.1016/0304-3835(94)03677-b] [Cited by in Crossref: 5] [Article Influence: 0.2] [Reference Citation Analysis]
397 O'connell P, Lathrop G, Law M, Leppert M, Nakamura Y, Hoff M, Kumlin E, Thomas W, Elsner T, Ballard L, Goodman P, Azen E, Sadler J, Cai G, Lalouel J, White R. A primary genetic linkage map for human chromosome 12. Genomics 1987;1:93-102. [DOI: 10.1016/0888-7543(87)90110-8] [Cited by in Crossref: 68] [Cited by in F6Publishing: 64] [Article Influence: 2.0] [Reference Citation Analysis]
398 Resnick IB, Aker M, Shapira MY, Tsirigotis PD, Bitan M, Abdul-hai A, Samuel S, Ackerstein A, Gesundheit B, Zilberman I, Miron S, Yoffe L, Lvovich A, Slavin S, Or R. Allogeneic stem cell transplantation for severe acquired aplastic anaemia using a fludarabine-based preparative regimen. Br J Haematol 2006;133:649-54. [DOI: 10.1111/j.1365-2141.2006.06084.x] [Cited by in Crossref: 40] [Cited by in F6Publishing: 32] [Article Influence: 2.7] [Reference Citation Analysis]
399 Murtagh JJ Jr, Eddy R, Shows TB, Moss J, Vaughan M. Different forms of Go alpha mRNA arise by alternative splicing of transcripts from a single gene on human chromosome 16. Mol Cell Biol 1991;11:1146-55. [PMID: 1899283 DOI: 10.1128/mcb.11.2.1146-1155.1991] [Cited by in F6Publishing: 7] [Reference Citation Analysis]
400 Amundson SA, Xia F, Wolfson K, Liber HL. Different cytotoxic and mutagenic responses induced by X-rays in two human lymphoblastoid cell lines derived from a single donor. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 1993;286:233-41. [DOI: 10.1016/0027-5107(93)90188-l] [Cited by in Crossref: 58] [Cited by in F6Publishing: 13] [Article Influence: 2.1] [Reference Citation Analysis]
401 Ledbetter SA, Wallace MR, Collins FS, Ledbetter DH. Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3. Genomics 1990;7:264-9. [DOI: 10.1016/0888-7543(90)90549-a] [Cited by in Crossref: 13] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
402 Sternlicht MD, Safarians S, Calcaterra TC, Barsky SH. Establishment and characterization of a novel human myoepithelial cell line and matrix-producing xenograft from a parotid basal cell adenocarcinoma. In Vitro Cell Dev Biol -Animal 1996;32:550-63. [DOI: 10.1007/bf02722982] [Cited by in Crossref: 18] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
403 van Belkum A, Scherer S, van Alphen L, Verbrugh H. Short-Sequence DNA Repeats in Prokaryotic Genomes. Microbiol Mol Biol Rev 1998;62:275-93. [DOI: 10.1128/mmbr.62.2.275-293.1998] [Cited by in Crossref: 471] [Cited by in F6Publishing: 200] [Article Influence: 20.5] [Reference Citation Analysis]
404 Caetano-anollés G, Brant J. B, Peter M. G. DNA Amplification Fingerprinting Using Very Short Arbitrary Oligonucleotide Primers. Nat Biotechnol 1991;9:553-7. [DOI: 10.1038/nbt0691-553] [Cited by in Crossref: 246] [Cited by in F6Publishing: 140] [Article Influence: 8.2] [Reference Citation Analysis]
405 Rogaev EI. Simple human DNA-repeats associated with genomic hypervariability, flanking the genomic retroposons and similar to retroviral sites. Nucleic Acids Res 1990;18:1879-85. [PMID: 2159624 DOI: 10.1093/nar/18.7.1879] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.3] [Reference Citation Analysis]
406 Bitan M, Or R, Shapira M, Aker M, Resnick I, Ackerstein A, Samuel S, Elad S, Slavin S. Fludarabine-Based Reduced Intensity Conditioning for Stem Cell Transplantation of Fanconi Anemia Patients from Fully Matched Related and Unrelated Donors. Biology of Blood and Marrow Transplantation 2006;12:712-8. [DOI: 10.1016/j.bbmt.2006.03.002] [Cited by in Crossref: 37] [Cited by in F6Publishing: 34] [Article Influence: 2.5] [Reference Citation Analysis]
407 Uitterlinden AG, Slagboom PE, Knook DL, Vijg J. Two-dimensional DNA fingerprinting of human individuals. Proc Natl Acad Sci U S A 1989;86:2742-6. [PMID: 2565037 DOI: 10.1073/pnas.86.8.2742] [Cited by in Crossref: 48] [Cited by in F6Publishing: 37] [Article Influence: 1.5] [Reference Citation Analysis]
408 Machin GA, Bamforth F. Zygosity and placental anatomy in 15 consecutive sets of spontaneously conceived triplets. Am J Med Genet 1996;61:247-52. [DOI: 10.1002/(sici)1096-8628(19960122)61:3<247::aid-ajmg8>3.0.co;2-r] [Cited by in Crossref: 26] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
409 Ewart AK, Morris CA, Atkinson D, Jin W, Sternes K, Spallone P, Stock AD, Leppert M, Keating MT. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nat Genet 1993;5:11-6. [DOI: 10.1038/ng0993-11] [Cited by in Crossref: 736] [Cited by in F6Publishing: 517] [Article Influence: 26.3] [Reference Citation Analysis]
410 Buffery C, Burridge F, Greenhalgh M, Jones S, Willow G. Allele frequency distributions of four variable number tandem repeat (VNTR) loci in the London. Forensic Science International 1991;52:53-64. [DOI: 10.1016/0379-0738(91)90096-2] [Cited by in Crossref: 24] [Cited by in F6Publishing: 9] [Article Influence: 0.8] [Reference Citation Analysis]
411 Dausset J, Cann H, Cohen D, Lathrop M, Lalouel JM, White R. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. Genomics 1990;6:575-7. [PMID: 2184120 DOI: 10.1016/0888-7543(90)90491-c] [Cited by in Crossref: 368] [Cited by in F6Publishing: 137] [Article Influence: 11.9] [Reference Citation Analysis]
412 Gelfi C, Cossu G, Carta P, Serra M, Righetti PG. Gene dosage in capillary electrophoresis: Pre-natal diagnosis of Down's syndrome. Journal of Chromatography A 1995;718:405-12. [DOI: 10.1016/0021-9673(95)00828-4] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 0.7] [Reference Citation Analysis]
413 Järvelä I, Schleutker J, Haataja L, Santavuori P, Puhakka L, Manninen T, Palotie A, Sandkuijl LA, Renlund M, White R. Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1. Genomics 1991;9:170-3. [PMID: 1672288 DOI: 10.1016/0888-7543(91)90235-7] [Cited by in Crossref: 94] [Cited by in F6Publishing: 71] [Article Influence: 3.1] [Reference Citation Analysis]
414 St George-hyslop PH, Myers RH, Haines JL, Farrer LA, Tanzi RE, Abe K, James MF, Conneally P, Polinsky RJ, Gusella JF. Familial Alzheimer's disease: Progress and problems. Neurobiology of Aging 1989;10:417-25. [DOI: 10.1016/0197-4580(89)90082-1] [Cited by in Crossref: 53] [Cited by in F6Publishing: 38] [Article Influence: 1.7] [Reference Citation Analysis]
415 Ledbetter SA, Nelson DL, Warren ST, Ledbetter DH. Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction. Genomics 1990;6:475-81. [DOI: 10.1016/0888-7543(90)90477-c] [Cited by in Crossref: 120] [Cited by in F6Publishing: 23] [Article Influence: 3.9] [Reference Citation Analysis]
416 Evans JD. Parentage analyses in ant colonies using simple sequence repeat loci. Mol Ecol 1993;2:393-7. [DOI: 10.1111/j.1365-294x.1993.tb00032.x] [Cited by in Crossref: 88] [Cited by in F6Publishing: 9] [Article Influence: 3.1] [Reference Citation Analysis]
417 Kunieda T, Kobayashi E, Tachibana M, Ikadai H, Imamichi T. Localization of the interleukin-3 gene to rat chromosome 10 by linkage analyses with a variable number of tandem repeats (VNTR). Mamm Genome 1992;3:464-6. [PMID: 1643309 DOI: 10.1007/BF00356158] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
418 Brouwer OF, Wijmenga C, Frants RR, Padberg GW. Facioscapulohumeral muscular dystrophy: the impact of genetic research. Clin Neurol Neurosurg 1993;95:9-21. [PMID: 8095870 DOI: 10.1016/0303-8467(93)90086-v] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
419 Sandberg AA, Meloni AM, Suijkerbuijk RF. Reviews of Chromosome Studies in Urological Tumors. III. Cytogenetics and Genes in Testicular Tumors. Journal of Urology 1996;155:1531-56. [DOI: 10.1016/s0022-5347(01)66124-x] [Cited by in Crossref: 91] [Article Influence: 3.6] [Reference Citation Analysis]
420 Denomme GA, Waye JS, Borrows RF, Hayward CPM, Warkentin TE, Horsewood P, Smith JW, Jelsema RD, Zuidema LJ, Kelton JG. The prenatal identification of fetal compatibility in neonatal alloimmune thrombocytopenia using amniotic fluid and variable number of tandem repeat (VNTR) analysis. Br J Haematol 1995;91:742-6. [DOI: 10.1111/j.1365-2141.1995.tb05379.x] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 0.5] [Reference Citation Analysis]
421 Nakamura Y, Martin C, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pCMM6) on chromosome 20 [D20S19]. Nucleic Acids Res 1988;16:5222. [PMID: 2898762 DOI: 10.1093/nar/16.11.5222] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 0.3] [Reference Citation Analysis]
422 Johnson JP. Genetic counseling using linked DNA probes: Cystic fibrosis as a prototype. The Journal of Pediatrics 1988;113:957-64. [DOI: 10.1016/s0022-3476(88)80563-8] [Cited by in Crossref: 6] [Article Influence: 0.2] [Reference Citation Analysis]
423 Devor EJ. Why there is no gene for alcoholism. Behav Genet 1993;23:145-51. [DOI: 10.1007/bf01067419] [Cited by in Crossref: 12] [Article Influence: 0.4] [Reference Citation Analysis]
424 Gualandi G, Santolini E, Calef E. Epstein-Barr virus DNA recombines via latent origin of replication with the human genome in the lymphoblastoid cell line RGN1. J Virol 1992;66:5677-81. [DOI: 10.1128/jvi.66.9.5677-5681.1992] [Cited by in Crossref: 10] [Article Influence: 0.3] [Reference Citation Analysis]
425 Uitterlinden AG, Vijg J. Denaturing gradient gel electrophoretic analysis of minisatellite alleles. Electrophoresis 1991;12:12-6. [DOI: 10.1002/elps.1150120104] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 0.4] [Reference Citation Analysis]
426 Nakamura Y. DNA variations in human and medical genetics: 25 years of my experience. J Hum Genet 2009;54:1-8. [PMID: 19158818 DOI: 10.1038/jhg.2008.6] [Cited by in Crossref: 44] [Cited by in F6Publishing: 25] [Article Influence: 3.7] [Reference Citation Analysis]
427 Levitt RC. Polymorphisms in the transcribed 3′ untranslated region of eukaryotic genes. Genomics 1991;11:484-9. [DOI: 10.1016/0888-7543(91)90168-e] [Cited by in Crossref: 19] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
428 MacLeod RA, Dirks WG, Matsuo Y, Kaufmann M, Milch H, Drexler HG. Widespread intraspecies cross-contamination of human tumor cell lines arising at source. Int J Cancer 1999;83:555-63. [PMID: 10508494 DOI: 10.1002/(sici)1097-0215(19991112)83:4<555::aid-ijc19>3.0.co;2-2] [Cited by in Crossref: 237] [Cited by in F6Publishing: 86] [Article Influence: 10.8] [Reference Citation Analysis]
429 Byerley WF. Genetic linkage revisited. Nature 1989;340:340-1. [DOI: 10.1038/340340a0] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 0.5] [Reference Citation Analysis]
430 Deka R, Chakroborty R, Ferrell RE. A population genetic study of six VNTR loci in three ethnically defined populations. Genomics 1991;11:83-92. [PMID: 1765387 DOI: 10.1016/0888-7543(91)90104-m] [Cited by in Crossref: 47] [Cited by in F6Publishing: 8] [Article Influence: 1.6] [Reference Citation Analysis]
431 Carvalho GR, Hauser L. Advances in the molecular analysis of fish population structure. Italian Journal of Zoology 1998;65:21-33. [DOI: 10.1080/11250009809386791] [Cited by in Crossref: 57] [Cited by in F6Publishing: 18] [Article Influence: 2.5] [Reference Citation Analysis]
432 Gleich LL, Li YQ, Biddinger PW, Gartside PS, Stambrook PJ, Pavelic ZP, Gluckman JL. The loss of heterozygosity in retinoblastoma and p53 suppressor genes as a prognostic indicator for head and neck cancer. Laryngoscope. 1996;106:1378-1381. [PMID: 8914904 DOI: 10.1097/00005537-199611000-00013] [Cited by in Crossref: 24] [Cited by in F6Publishing: 18] [Article Influence: 1.0] [Reference Citation Analysis]
433 Tourmente S, Deragon JM, Lafleuriel J, Tutois S, Pélissier T, Cuvillier C, Espagnol MC, Picard G. Characterization of minisatellites in Arabidopsis thaliana with sequence similarity to the human minisatellite core sequence. Nucleic Acids Res 1994;22:3317-21. [PMID: 8078766 DOI: 10.1093/nar/22.16.3317] [Cited by in Crossref: 14] [Cited by in F6Publishing: 8] [Article Influence: 0.5] [Reference Citation Analysis]
434 Cropp CS, Lidereau R, Campbell G, Champene MH, Callahan R. Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified. Proc Natl Acad Sci USA. 1990;87:7737-7741. [PMID: 1977164 DOI: 10.1073/pnas.87.19.7737] [Cited by in Crossref: 72] [Cited by in F6Publishing: 75] [Article Influence: 2.3] [Reference Citation Analysis]
435 Friar E, Kochert G. Bamboo germplasm screening with nuclear restriction fragment length polymorphisms. Theor Appl Genet 1991;82:697-703. [PMID: 24213443 DOI: 10.1007/BF00227313] [Cited by in Crossref: 24] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
436 Smith J, Anwar R, Riley J, Jenner D, Markham A, Jeffreys A. Highly polymorphic minisatellite sequences: allele frequencies and mutation rates for five locus-specific probes in a Caucasian population. Journal of the Forensic Science Society 1990;30:19-32. [DOI: 10.1016/s0015-7368(90)73298-7] [Cited by in Crossref: 50] [Cited by in F6Publishing: 4] [Article Influence: 1.6] [Reference Citation Analysis]
437 Vosman B, Arens P, Rus-Kortekaas W, Smulders MJ. Identification of highly polymorphic DNA regions in tomato. Theor Appl Genet 1992;85:239-44. [PMID: 24197310 DOI: 10.1007/BF00222865] [Cited by in Crossref: 39] [Cited by in F6Publishing: 8] [Article Influence: 4.9] [Reference Citation Analysis]
438 Knowlton RG, Nelson CA, Brown VA, Page DC, Donis-Keller H. An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome. Nucleic Acids Res 1989;17:423-37. [PMID: 2911472 DOI: 10.1093/nar/17.1.423] [Cited by in Crossref: 37] [Cited by in F6Publishing: 34] [Article Influence: 1.2] [Reference Citation Analysis]
439 de Lange T, Shiue L, Myers RM, Cox DR, Naylor SL, Killery AM, Varmus HE. Structure and variability of human chromosome ends. Mol Cell Biol 1990;10:518-27. [PMID: 2300052 DOI: 10.1128/mcb.10.2.518-527.1990] [Cited by in Crossref: 4] [Cited by in F6Publishing: 212] [Article Influence: 0.1] [Reference Citation Analysis]
440 Dracopoli NC, Harnett P, Bale SJ, Stanger BZ, Tucker MA, Housman DE, Kefford RF. Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression. Proc Natl Acad Sci U S A 1989;86:4614-8. [PMID: 2734311 DOI: 10.1073/pnas.86.12.4614] [Cited by in Crossref: 144] [Cited by in F6Publishing: 135] [Article Influence: 4.5] [Reference Citation Analysis]
441 Collick A, Dunn MG, Jeffreys AJ. Minisatellite binding protein Msbp-1 is a sequence-specific single-stranded DNA-binding protein. Nucleic Acids Res 1991;19:6399-404. [PMID: 1754375 DOI: 10.1093/nar/19.23.6399] [Cited by in Crossref: 23] [Cited by in F6Publishing: 25] [Article Influence: 0.8] [Reference Citation Analysis]
442 Kurosawa K, Kuromaru R, Imaizumi K, Nakamura Y, Ishikawa F, Ueda K, Kuroki Y. Monozygotic Twins with Discordant Sex. Acta genet med gemellol : twin res 1992;41:301-10. [DOI: 10.1017/s0001566000002154] [Cited by in Crossref: 19] [Article Influence: 2.7] [Reference Citation Analysis]
443 Steele MR, Georges M. Generation of bovine multisite haplotypes using random cosmid clones. Genomics 1991;10:889-904. [DOI: 10.1016/0888-7543(91)90177-g] [Cited by in Crossref: 16] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
444 Khan FA, Varma GM, Vijay IK. Genomic organization and promoter activity of glucosidase I gene. Glycobiology 1999;9:797-806. [PMID: 10406845 DOI: 10.1093/glycob/9.8.797] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
445 Sajantila A, Budowle B. Identification of Individuals with DNA Testing. Annals of Medicine 2009;23:637-42. [DOI: 10.3109/07853899109148096] [Cited by in Crossref: 16] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
446 Fujii H, Shimada T. Isolation and characterization of cDNA clones derived from the divergently transcribed gene in the region upstream from the human dihydrofolate reductase gene. Journal of Biological Chemistry 1989;264:10057-64. [DOI: 10.1016/s0021-9258(18)81766-5] [Cited by in Crossref: 79] [Article Influence: 2.5] [Reference Citation Analysis]
447 Lupski JR, Weinstock GM. Short, interspersed repetitive DNA sequences in prokaryotic genomes. J Bacteriol 1992;174:4525-9. [PMID: 1624445 DOI: 10.1128/jb.174.14.4525-4529.1992] [Cited by in Crossref: 228] [Cited by in F6Publishing: 151] [Article Influence: 7.9] [Reference Citation Analysis]
448 Thiart R, Varret M, Lintott C, Scott R, Loubser O, du Plessis L, de Villiers J, Boileau C, Kotze M. Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia. Molecular and Cellular Probes 2000;14:299-304. [DOI: 10.1006/mcpr.2000.0318] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
449 Bruford MW, Altmann J. DNA fingerprinting and the problems of paternity determination in an inbred captive population of guinea baboons (Papio hamadryas papio). Primates 1993;34:403-11. [DOI: 10.1007/bf02382636] [Cited by in Crossref: 3] [Article Influence: 0.1] [Reference Citation Analysis]
450 Minelli A, Floridia G, Rossi E, Clementi M, Tenconi R, Camurri L, Bernardi F, Hoeller H, Previde Re C, Maraschio P, Wood S, Zuffardi O, Danesino C. D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Hum Genet 1993;92:391-6. [DOI: 10.1007/bf01247342] [Cited by in Crossref: 23] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
451 Miki Y, Nishisho I, Nakamura Y, Miyoshi Y, Utsunomiya J. Interstitial loss of the same region of 5q in multiple adenomas and a carcinoma derived from an adenomatous polyposis coli (apc) patient. Genes Chromosom Cancer 1992;4:81-3. [DOI: 10.1002/gcc.2870040112] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.3] [Reference Citation Analysis]
452 Kashi Y, Lipkin E, Darvasi A, Nave A, Gruenbaum Y, Beckmann J, Soller M. Parentage Identification in the Bovine Using “Deoxyribonucleic Acid Fingerprints”. Journal of Dairy Science 1990;73:3306-11. [DOI: 10.3168/jds.s0022-0302(90)79024-8] [Cited by in Crossref: 11] [Article Influence: 0.4] [Reference Citation Analysis]
453 Longmire JL, Brown NC, Meincke LJ, Campbell ML, Albright KL, Fawcett JJ, Campbell EW, Moyzis RK, Hildebrand CE, Evans GA, Deaven LL. Construction and characterization of partial digest DNA libraries made from flow-sorted human chromosome 16. Genetic Analysis: Biomolecular Engineering 1993;10:69-76. [DOI: 10.1016/1050-3862(93)90037-j] [Cited by in Crossref: 24] [Cited by in F6Publishing: 5] [Article Influence: 0.9] [Reference Citation Analysis]
454 Mills K, Buetow K, Xu Y, Weber J, Altherr M, Wasmuth J, Murray J. Genetic and physical maps of human chromosome 4 based on dinucleotide repeats. Genomics 1992;14:209-19. [DOI: 10.1016/s0888-7543(05)80208-3] [Cited by in Crossref: 26] [Cited by in F6Publishing: 9] [Article Influence: 0.9] [Reference Citation Analysis]
455 Ball AO, Beard CW, Villegas P, Spindler KR. Early region 4 sequence and biological comparison of two isolates of mouse adenovirus type 1. Virology 1991;180:257-65. [DOI: 10.1016/0042-6822(91)90030-f] [Cited by in Crossref: 22] [Cited by in F6Publishing: 14] [Article Influence: 0.7] [Reference Citation Analysis]
456 Mancuso DJ, Tuley EA, Westfield LA, Worrall NK, Shelton-inloes BB, Sorace JM, Alevy YG, Sadler JE. Structure of the gene for human von Willebrand factor. Journal of Biological Chemistry 1989;264:19514-27. [DOI: 10.1016/s0021-9258(19)47144-5] [Cited by in Crossref: 186] [Article Influence: 5.8] [Reference Citation Analysis]
457 Batzer MA, Stoneking M, Alegria-Hartman M, Bazan H, Kass DH, Shaikh TH, Novick GE, Ioannou PA, Scheer WD, Herrera RJ. African origin of human-specific polymorphic Alu insertions. Proc Natl Acad Sci USA. 1994;91:12288-12292. [PMID: 7991620 DOI: 10.1073/pnas.91.25.12288] [Cited by in Crossref: 197] [Cited by in F6Publishing: 150] [Article Influence: 7.6] [Reference Citation Analysis]
458 Gonnaud PM, Sturtz F, Fourbil Y, Bonnebouche C, Tranchant C, Warter JM, Chazot G, Bady B, Vial C, Brechard AS. DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations. Acta Neurol Scand 1995;92:313-8. [PMID: 8848937 DOI: 10.1111/j.1600-0404.1995.tb00135.x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
459 Valverde E, Cabrero C, Cao R, Rodríguez-Calvo MS, Díez A, Barros F, Alemany J, Carracedo A. Population genetics of three VNTR polymorphisms in two different Spanish populations. Int J Legal Med 1993;105:251-6. [PMID: 8471542 DOI: 10.1007/BF01370381] [Cited by in Crossref: 26] [Cited by in F6Publishing: 2] [Article Influence: 0.9] [Reference Citation Analysis]
460 Chandley AC. Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man. J Med Genet 1989;26:546-52. [PMID: 2681783 DOI: 10.1136/jmg.26.9.546] [Cited by in Crossref: 33] [Cited by in F6Publishing: 28] [Article Influence: 1.0] [Reference Citation Analysis]
461 Yamakawa K, Takahashi E, Murata M, Okui K, Yokoyama S, Nakamura Y. Detailed mapping around the breakpoint of (3;8) translocation in familial renal cell carcinoma and FRA3B. Genomics 1992;14:412-6. [PMID: 1427857 DOI: 10.1016/s0888-7543(05)80234-4] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
462 Pötsch L, Meyer U, Rothschild S, Schneider PM, Rittner C. Application of DNA techniques for identification using human dental pulp as a source of DNA. Int J Legal Med 1992;105:139-43. [PMID: 1419874 DOI: 10.1007/BF01625165] [Cited by in Crossref: 56] [Cited by in F6Publishing: 5] [Article Influence: 1.9] [Reference Citation Analysis]
463 King M. An Application of DNA Sequencing to a Human Rights Problem. Molecular Genetic Medicine. Elsevier; 1991. pp. 117-31. [DOI: 10.1016/b978-0-12-462001-8.50009-0] [Cited by in Crossref: 13] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
464 Shapira MY, Resnick IB, Dray L, Aker M, Stepensky P, Elad S, Gesundeheidt B, Samuel S, Or R. A new induction protocol for the control of steroid refractory/dependent acute graft versus host disease with alefacept and tacrolimus. Cytotherapy 2009;11:61-7. [PMID: 19191054 DOI: 10.1080/14653240802644669] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 0.9] [Reference Citation Analysis]
465 Gill P, Woodroffe S, Bär W, Brinkmann B, Carracedo A, Eriksen B, Jones S, Kloosterman A, Ludes B, Mevag B, Pascali V, Rudler M, Schmitter H, Schneider P, Thomson J. A report of an international collaborative experiment to demonstrate the uniformity obtainable using DNA profiling techniques. Forensic Science International 1992;53:29-43. [DOI: 10.1016/0379-0738(92)90130-o] [Cited by in Crossref: 35] [Cited by in F6Publishing: 1] [Article Influence: 1.2] [Reference Citation Analysis]
466 Kim W, Hong YP, Yoo JH, Lee WB, Choi CS, Chung SI. Genetic relationships of Bacillus anthracis and closely related species based on variable-number tandem repeat analysis and BOX-PCR genomic fingerprinting. FEMS Microbiol Lett 2002;207:21-7. [PMID: 11886745 DOI: 10.1111/j.1574-6968.2002.tb11022.x] [Cited by in Crossref: 29] [Cited by in F6Publishing: 26] [Article Influence: 1.5] [Reference Citation Analysis]
467 Kato MV, Ishizaki K, Shimizu T, Ejima Y, Tanooka H, Takayama J, Kaneko A, Toguchida J, Sasaki MS, Kato MV. Parental origin of germ-line and somatic mutations in the retinoblastoma gene. Hum Genet 1994;94:31-8. [DOI: 10.1007/bf02272838] [Cited by in Crossref: 34] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
468 Shapero MH, Kundu SK, Engleman E, Laus R, Van Schooten WCA, Merigan TC. In Vivo Persistence of Donor Cells following Adoptive Transfer of Allogeneic Dendritic Cells in HIV-Infected Patients. Cell Transplant 2000;9:307-17. [DOI: 10.1177/096368970000900302] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
469 Lathrop G, Lalouel J. 4 Statistical methods for linkage analysis. Statistical Methods in Biological and Medical Sciences. Elsevier; 1991. pp. 81-123. [DOI: 10.1016/s0169-7161(05)80160-9] [Cited by in Crossref: 6] [Article Influence: 0.2] [Reference Citation Analysis]
470 Wildrick DM. Molecular Genetic Studies of Colon Cancer. Hematology/Oncology Clinics of North America 1989;3:1-18. [DOI: 10.1016/s0889-8588(18)30564-1] [Cited by in Crossref: 5] [Article Influence: 0.2] [Reference Citation Analysis]
471 Nakamura Y, Lathrop M, O'connell P, Leppert M, Kamboh M, Lalouel J, White R. Frequent recombination is observed in the distal end of the long arm of chromosome 14. Genomics 1989;4:76-81. [DOI: 10.1016/0888-7543(89)90317-0] [Cited by in Crossref: 33] [Cited by in F6Publishing: 37] [Article Influence: 1.0] [Reference Citation Analysis]
472 Haberfeld A, Hillel J. Development of DNA fingerprint probes: An approach and its application. Animal Biotechnology 1991;2:61-73. [DOI: 10.1080/10495399109525748] [Cited by in Crossref: 18] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
473 Fong CT, Dracopoli NC, White PS, Merrill PT, Griffith RC, Housman DE, Brodeur GM. Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification. Proc Natl Acad Sci U S A 1989;86:3753-7. [PMID: 2566996 DOI: 10.1073/pnas.86.10.3753] [Cited by in Crossref: 248] [Cited by in F6Publishing: 228] [Article Influence: 7.8] [Reference Citation Analysis]
474 van Tuinen P, Rich DC, Summers KM, Ledbetter DH. Regional mapping panel for human chromosome 17: application to neurofibromatosis type 1. Genomics 1987;1:374-81. [PMID: 3130306 DOI: 10.1016/0888-7543(87)90042-5] [Cited by in Crossref: 64] [Cited by in F6Publishing: 65] [Article Influence: 1.9] [Reference Citation Analysis]
475 Gendler S, Lancaster C, Taylor-papadimitriou J, Duhig T, Peat N, Burchell J, Pemberton L, Lalani E, Wilson D. Molecular cloning and expression of human tumor-associated polymorphic epithelial mucin. Journal of Biological Chemistry 1990;265:15286-93. [DOI: 10.1016/s0021-9258(18)77254-2] [Cited by in Crossref: 397] [Article Influence: 12.8] [Reference Citation Analysis]
476 Keating M. Genetics of the Long QT Syndrome. J Cardiovasc Electrophysiol 1994;5:146-53. [DOI: 10.1111/j.1540-8167.1994.tb01155.x] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 0.4] [Reference Citation Analysis]
477 Strathdee CA, Duncan AM, Buchwald M. Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nat Genet. 1992;1:196-198. [PMID: 1303234 DOI: 10.1038/ng0692-196] [Cited by in Crossref: 214] [Cited by in F6Publishing: 181] [Article Influence: 7.6] [Reference Citation Analysis]
478 Mckusick VA, Harper PS. History of Medical Genetics. Emery and Rimoin's Principles and Practice of Medical Genetics. Elsevier; 2013. pp. 1-39. [DOI: 10.1016/b978-0-12-383834-6.00001-x] [Cited by in Crossref: 3] [Article Influence: 0.4] [Reference Citation Analysis]
479 N�rnberg P, Roewer L, Neitzel H, Sperling K, P�pperl A, Hundrieser J, P�che H, Epplen C, Zischler H, Epplen J. DNA Fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations. Hum Genet 1989;84:75-8. [DOI: 10.1007/bf00210676] [Cited by in Crossref: 72] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
480 Srivastava J, Premi S, Pathak D, Ahsan Z, Tiwari M, Garg LC, Ali S. Transcriptional Status of Known and Novel Genes Tagged with Consensus of 33.15 Repeat Loci Employing Minisatellite-Associated Sequence Amplification (MASA) and Real-Time PCR in Water Buffalo, Bubalus bubalis. DNA and Cell Biology 2006;25:31-48. [DOI: 10.1089/dna.2006.25.31] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 0.7] [Reference Citation Analysis]
481 Hinds HL, Hendriks RW, Craig IW, Chen ZY. Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif. Genomics 1992;13:896-7. [PMID: 1639424 DOI: 10.1016/0888-7543(92)90181-q] [Cited by in Crossref: 51] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
482 Nakamura Y, Culver M, Gillilan S, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence pYNZ23 to chromosome 1 (DIS58). Nucleic Acids Res 1987;15:9620. [PMID: 2446266 DOI: 10.1093/nar/15.22.9620] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 0.1] [Reference Citation Analysis]
483 Or R, Shapira MY, Resnick I, Amar A, Ackerstein A, Samuel S, Aker M, Naparstek E, Nagler A, Slavin S. Nonmyeloablative allogeneic stem cell transplantation for the treatment of chronic myeloid leukemia in first chronic phase. Blood. 2003;101:441-445. [PMID: 12393604 DOI: 10.1182/blood-2002-02-0535] [Cited by in Crossref: 152] [Cited by in F6Publishing: 109] [Article Influence: 8.0] [Reference Citation Analysis]
484 Turri MG, Cuin KA, Porter AC. Characterisation of a novel minisatellite that provides multiple splice donor sites in an interferon-induced transcript. Nucleic Acids Res 1995;23:1854-61. [PMID: 7596809 DOI: 10.1093/nar/23.11.1854] [Cited by in Crossref: 27] [Cited by in F6Publishing: 20] [Article Influence: 1.0] [Reference Citation Analysis]
485 Saito H, Moses RE. Immortalization of Werner syndrome and progeria fibroblasts. Experimental Cell Research 1991;192:373-9. [DOI: 10.1016/0014-4827(91)90054-x] [Cited by in Crossref: 26] [Cited by in F6Publishing: 10] [Article Influence: 0.9] [Reference Citation Analysis]
486 Treiman LJ. Genetics of Epilepsy: An Overview. Epilepsia 1993;34:S1-S11. [DOI: 10.1111/j.1528-1167.1993.tb06254.x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
487 Smith J, Newton C, Alves A, Anwar R, Jenner D, Markham A. Highly polymorphic minisatellite DNA probes. Further evaluation for individual identification and paternity testing. Journal of the Forensic Science Society 1990;30:3-18. [DOI: 10.1016/s0015-7368(90)73297-5] [Cited by in Crossref: 39] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
488 van Leeuwen JEM, van Tol MJD, Bodzinga BG, Wijnen JT, Keur MVD, Joosten AM, Tanke HJ, Vossen JM, Khan PM. Detection of mixed chimaerism in flow-sorted cell subpopulations by PCR-amplified VNTR markers after allogeneic bone marrow transplantation. Br J Haematol 1991;79:218-25. [DOI: 10.1111/j.1365-2141.1991.tb04525.x] [Cited by in Crossref: 38] [Cited by in F6Publishing: 29] [Article Influence: 1.3] [Reference Citation Analysis]
489 von Beroldingen CH, Blake ET, Higuchi R, Sensabaugh GF, Erlich H. Applications of PCR to the Analysis of Biological Evidence. In: Erlich HA, editor. PCR Technology. London: Palgrave Macmillan UK; 1989. pp. 209-23. [DOI: 10.1007/978-1-349-20235-5_17] [Cited by in Crossref: 29] [Cited by in F6Publishing: 9] [Article Influence: 0.9] [Reference Citation Analysis]
490 Li H, Hood L. Multiplex genotype determination at a DNA sequence polymorphism cluster in the human immunoglobulin heavy-chain region. Genomics 1995;26:199-206. [PMID: 7601443 DOI: 10.1016/0888-7543(95)80201-v] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 0.3] [Reference Citation Analysis]
491 Eubanks JH, Selleri L, Hart R, Rosette C, Evans GA. Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13. Genomics 1991;11:720-9. [DOI: 10.1016/0888-7543(91)90080-x] [Cited by in Crossref: 22] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
492 Ryan AM, Womack JE. Type I interferon genes in cattle: restriction fragment length polymorphisms, gene numbers and physical organization on bovine chromosome 8. Animal Genetics 1993;24:9-16. [DOI: 10.1111/j.1365-2052.1993.tb00912.x] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 1.4] [Reference Citation Analysis]
493 Stacey GN, Bolton BJ, Doyle A. DNA fingerprinting transforms the art of cell authentication. Nature 1992;357:261-2. [DOI: 10.1038/357261a0] [Cited by in Crossref: 39] [Cited by in F6Publishing: 26] [Article Influence: 1.3] [Reference Citation Analysis]
494 Destro-bisol G, Belledi M, Capelli C, Maviglia R, Spedini G. Genetic variation at the ApoB 3? HVR minisatellite locus in the Mbenzele Pygmies from the Central African Republic. Am J Hum Biol 2000;12:588-92. [DOI: 10.1002/1520-6300(200009/10)12:5<588::aid-ajhb2>3.0.co;2-v] [Cited by in Crossref: 3] [Article Influence: 0.1] [Reference Citation Analysis]
495 Resnick IB, Aker M, Tsirigotis P, Shapira MY, Abdul-hai A, Bitan M, Gesundheit B, Amar A, Ackerstein A, Samuel S, Slavin S, Or R. Allogeneic stem cell transplantation from matched related and unrelated donors in thalassemia major patients using a reduced toxicity fludarabine-based regimen. Bone Marrow Transplant 2007;40:957-64. [DOI: 10.1038/sj.bmt.1705826] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 1.2] [Reference Citation Analysis]
496 Malkhosyan S, Yasuda J, Soto JL, Sekiya T, Yokota J, Perucho M. Molecular karyotype (amplotype) of metastatic colorectal cancer by unbiased arbitrarily primed PCR DNA fingerprinting. Proc Natl Acad Sci U S A 1998;95:10170-5. [PMID: 9707619 DOI: 10.1073/pnas.95.17.10170] [Cited by in Crossref: 39] [Cited by in F6Publishing: 37] [Article Influence: 1.7] [Reference Citation Analysis]
497 Hanotte O, Bruford MW, Burke T. Multilocus DNA fingerprints in gallinaceous birds: general approach and problems. Heredity 1992;68:481-94. [DOI: 10.1038/hdy.1992.71] [Cited by in Crossref: 32] [Cited by in F6Publishing: 9] [Article Influence: 1.1] [Reference Citation Analysis]
498 Nakamura Y, Fujimoto E, Ballard L, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence pEFD4.2 on chromosome 19 [D19S22]. Nucleic Acids Res 1988;16:1228. [PMID: 2894013 DOI: 10.1093/nar/16.3.1228] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
499 Domaniç NO, Preparata FP. A novel approach to the detection of genomic approximate tandem repeats in the Levenshtein metric. J Comput Biol 2007;14:873-91. [PMID: 17803368 DOI: 10.1089/cmb.2007.0018] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
500 Schafer AJ, Hawkins JR. DNA variation and the future of human genetics. Nat Biotechnol 1998;16:33-9. [DOI: 10.1038/nbt0198-33] [Cited by in Crossref: 143] [Cited by in F6Publishing: 125] [Article Influence: 6.2] [Reference Citation Analysis]
501 Nelson RP, Yu M, Schwartz JE, Robertson MJ, Hromas R, Fausel CA, Vance GH, Dlouhy SR, Baute JA, Cox EA, Wood LL, Srivastava S, Robertson KA, Haut PR, Farag SS, Abonour R, Cornetta K, Cripe LD. Long-term disease-free survival after nonmyeloablative cyclophosphamide/fludarabine conditioning and related/unrelated allotransplantation for acute myeloid leukemia/myelodysplasia. Bone Marrow Transplant 2010;45:1300-8. [DOI: 10.1038/bmt.2009.348] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 1.2] [Reference Citation Analysis]
502 Beckmann JS, Soller M. Toward a unified approach to genetic mapping of eukaryotes based on sequence tagged microsatellite sites. Biotechnology (N Y) 1990;8:930-2. [PMID: 1366775 DOI: 10.1038/nbt1090-930] [Cited by in Crossref: 71] [Cited by in F6Publishing: 49] [Article Influence: 2.4] [Reference Citation Analysis]
503 Heath DD, Iwama GK, Devlin RH. PCR primed with VNTR core sequences yields species specific patterns and hypervariable probes. Nucleic Acids Res 1993;21:5782-5. [PMID: 8284229 DOI: 10.1093/nar/21.24.5782] [Cited by in Crossref: 120] [Cited by in F6Publishing: 50] [Article Influence: 4.4] [Reference Citation Analysis]
504 Fahsold R, Rott HD, Lorenz P. A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locus. Hum Genet 1991;88:85-90. [PMID: 1959929 DOI: 10.1007/BF00204934] [Cited by in Crossref: 35] [Cited by in F6Publishing: 4] [Article Influence: 1.2] [Reference Citation Analysis]
505 . The human gene map. Phil Trans R Soc Lond B 1988;319:229-37. [DOI: 10.1098/rstb.1988.0045] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
506 Vergnaud G, Mariat D, Zoroastro M, Lauthier V. Detection of single and multiple polymorphic loci by synthetic tandem repeats of short oligonucleotides. Electrophoresis 1991;12:134-40. [DOI: 10.1002/elps.1150120207] [Cited by in Crossref: 17] [Cited by in F6Publishing: 11] [Article Influence: 0.6] [Reference Citation Analysis]
507 Fowler C, Drinkwater R, Skinner J, Burgoyne L. Human satellite-III DNA: an example of a "macrosatellite" polymorphism. Hum Genet 1988;79:265-72. [PMID: 2841225 DOI: 10.1007/BF00366249] [Cited by in Crossref: 12] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
508 Bochud M. Genetics for clinicians: from candidate genes to whole genome scans (technological advances). Best Pract Res Clin Endocrinol Metab 2012;26:119-32. [PMID: 22498243 DOI: 10.1016/j.beem.2011.09.001] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
509 Atluri S, Neville K, Davis M, Robertson KA, Marshalleck FE, O'malley DP, Buckley RH, Nelson RP. Epstein-Barr–associated Leiomyomatosis and T-cell Chimerism After Haploidentical Bone Marrow Transplantation for Severe Combined Immunodeficiency Disease. Journal of Pediatric Hematology/Oncology 2007;29:166-72. [DOI: 10.1097/mph.0b013e31803b95b3] [Cited by in Crossref: 10] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
510 Partridge M, Kiguwa S, Langdon J. Frequent deletion of chromosome 3p in oral squamous cell carcinoma. European Journal of Cancer Part B: Oral Oncology 1994;30:248-51. [DOI: 10.1016/0964-1955(94)90006-x] [Cited by in Crossref: 22] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
511 Yamakawa K, Morita R, Takahashi E, Hori T, Lathrop M, Nakamura Y. A genetic linkage map of 41 restriction fragment length polymorphism markers for human chromosome 3. Genomics 1991;11:565-72. [PMID: 1685476 DOI: 10.1016/0888-7543(91)90063-k] [Cited by in Crossref: 17] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
512 Nørby S, Schwartz M. Possible locus for polycystic kidney disease on chromosome 2. Lancet 1990;336:323-4. [PMID: 1974020 DOI: 10.1016/0140-6736(90)91870-g] [Cited by in Crossref: 20] [Cited by in F6Publishing: 6] [Article Influence: 0.6] [Reference Citation Analysis]
513 Pena SD, Macedo AM, Gontijo NF, Medeiros AM, Ribeiro JC. DNA bioprints: simple nonisotopic DNA fingerprints with biotinylated probes. Electrophoresis 1991;12:146-52. [PMID: 2040262 DOI: 10.1002/elps.1150120209] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 0.6] [Reference Citation Analysis]
514 Maquet A, Bi IZ, Rocha OJ, Baudoin JP. Case studies on breeding systems and its consequences for germplasm conservation: I. Isoenzyme diversity in wild Lima bean populations in central Costa Rica. Genet Resour Crop Evol 1996;43:309-18. [DOI: 10.1007/bf00132950] [Cited by in Crossref: 7] [Article Influence: 0.3] [Reference Citation Analysis]
515 Julier C, Nakamura Y, Lathrop M, O'connell P, Leppert M, Mohandas T, Lalouel J, White R. A primary map of 24 loci on human chromosome 16. Genomics 1990;6:419-27. [DOI: 10.1016/0888-7543(90)90471-6] [Cited by in Crossref: 28] [Cited by in F6Publishing: 27] [Article Influence: 0.9] [Reference Citation Analysis]
516 Naga Chaithanya MV, Sailaja D, Dinesh MR, Vasugi C, Lakshmana Reddy DC, Aswath C. Microsatellite-Based DNA Fingerprinting of Guava (Psidium guajava) Genotypes. Proc Natl Acad Sci , India, Sect B Biol Sci 2017;87:859-67. [DOI: 10.1007/s40011-015-0660-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
517 Sertedaki A, Lindsay S. CAC - the neglected repeat. Bioessays 1996;18:237-42. [DOI: 10.1002/bies.950180311] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
518 Denoeud F, Vergnaud G, Benson G. Predicting human minisatellite polymorphism. Genome Res 2003;13:856-67. [PMID: 12695323 DOI: 10.1101/gr.574403] [Cited by in Crossref: 32] [Cited by in F6Publishing: 28] [Article Influence: 1.8] [Reference Citation Analysis]
519 Mouhamadou B, Férandon C, Chazoule S, Barroso G. Unusual accumulation of polymorphic microsatellite loci in a specific region of the mitochondrial genome of two mushroom-forming Agrocybe species. FEMS Microbiol Lett 2007;272:276-81. [PMID: 17559401 DOI: 10.1111/j.1574-6968.2007.00771.x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
520 Sugano K, Nakashima Y, Yamaguchi K, Fukayama N, Maekawa M, Ohkura H, Kakizoe T, Sekiya T. Sensitive detection of loss of heterozygosity in theTP53 gene in pancreatic adenocarcinoma by fluorescence-based single-strand conformation polymorphism analysis using blunt-end DNA fragments. Genes Chromosom Cancer 1996;15:157-64. [DOI: 10.1002/(sici)1098-2264(199603)15:3<157::aid-gcc2>3.0.co;2-1] [Cited by in Crossref: 25] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
521 Hudson TJ, Engelstein M, Lee MK, Ho EC, Rubenfield MJ, Adams CP, Housman DE, Dracopoli NC. Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics 1992;13:622-9. [DOI: 10.1016/0888-7543(92)90133-d] [Cited by in Crossref: 155] [Cited by in F6Publishing: 35] [Article Influence: 5.3] [Reference Citation Analysis]
522 Ohara K, Xu H, Matsunaga T, Xu D, Huang X, Gu G, Ohara K, Wang Z. Cerebral ventricle-brain ratio in monozygotic twins discordant and concordant for schizophrenia. Progress in Neuro-Psychopharmacology and Biological Psychiatry 1998;22:1043-50. [DOI: 10.1016/s0278-5846(98)00048-7] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
523 Agematsu K, Nakahori Y. Recipient origin of bone marrow-derived fibroblastic stromal cells during all periods following bone marrow transplantation in humans. Br J Haematol. 1991;79:359-365. [PMID: 1751363 DOI: 10.1111/j.1365-2141.1991.tb08041.x] [Cited by in Crossref: 50] [Cited by in F6Publishing: 44] [Article Influence: 1.7] [Reference Citation Analysis]
524 Chakraborty R, Fornage M, Gueguen R, Boerwinkle E. Population Genetics of Hypervariable Loci: Analysis of PCR Based VNTR Polymorphism Within a Population. In: Burke T, Dolf G, Jeffreys AJ, Wolff R, editors. DNA Fingerprinting: Approaches and Applications. Basel: Birkhäuser; 1991. pp. 127-43. [DOI: 10.1007/978-3-0348-7312-3_10] [Cited by in Crossref: 85] [Cited by in F6Publishing: 27] [Article Influence: 2.8] [Reference Citation Analysis]
525 Chen P, Hurst T, Khoo SK. Detection of somatic DNA alterations in ovarian cancer by DNA fingerprint analysis. Cancer 1991;67:1551-5. [PMID: 2001544 DOI: 10.1002/1097-0142(19910315)67:6<1551::aid-cncr2820670615>3.0.co;2-5] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
526 Collick A, Jeffreys AJ. Detection of a novel minisatellite-specific DNA-binding protein. Nucleic Acids Res 1990;18:625-9. [PMID: 2308848 DOI: 10.1093/nar/18.3.625] [Cited by in Crossref: 37] [Cited by in F6Publishing: 36] [Article Influence: 1.2] [Reference Citation Analysis]
527 Takahashi E, Yamakawa K, Nakamura Y, Hori T. A high-resolution cytogenetic map of human chromosome 3: localization of 291 new cosmid markers by direct R-banding fluorescence in situ hybridization. Genomics 1992;13:1047-55. [PMID: 1354637 DOI: 10.1016/0888-7543(92)90018-n] [Cited by in Crossref: 28] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
528 Timmons CF, Dawson DB, Richards CS, Andrews WS, Katz JA. Epstein-Barr virus-associated leiomyosarcomas in liver transplantation recipients. Origin from either donor or recipient tissue. Cancer 1995;76:1481-9. [PMID: 8620427 DOI: 10.1002/1097-0142(19951015)76:8<1481::aid-cncr2820760828>3.0.co;2-k] [Cited by in Crossref: 71] [Cited by in F6Publishing: 8] [Article Influence: 2.8] [Reference Citation Analysis]
529 Ranzani GN, Renault B, Pellegata NS, Fattorini P, Magni E, Bacci F, Amadori D. Loss of heterozygosity and K-ras gene mutations in gastric cancer. Hum Genet. 1993;92:244-249. [PMID: 8406432 DOI: 10.1007/bf00244466] [Cited by in Crossref: 30] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
530 Perlman EJ, Stetten G, Tuck-Müller CM, Farber RA, Neuman WL, Blakemore KJ, Hutchins GM. Sexual discordance in monozygotic twins. Am J Med Genet 1990;37:551-7. [PMID: 1979713 DOI: 10.1002/ajmg.1320370427] [Cited by in Crossref: 31] [Cited by in F6Publishing: 19] [Article Influence: 1.0] [Reference Citation Analysis]
531 Rosenbaum HC, Deinard AS. Caution before claim: an overview of microsatellite analysis in ecology and evolutionary biology. In: Desalle R, Schierwater B, editors. Molecular Approaches to Ecology and Evolution. Basel: Birkhäuser; 1998. pp. 87-106. [DOI: 10.1007/978-3-0348-8948-3_5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
532 Holm T, Nakamura Y, Ballard L, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pTHI54) on chromosome 1p [D1S62]. Nucleic Acids Res 1988;16:3115. [PMID: 2897108 DOI: 10.1093/nar/16.7.3115] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.1] [Reference Citation Analysis]
533 Lupski JR, Garcia CA, Zoghbi HY, Hoffman EP, Fenwick RG. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy. Am J Med Genet 1991;40:354-64. [PMID: 1683155 DOI: 10.1002/ajmg.1320400323] [Cited by in Crossref: 54] [Cited by in F6Publishing: 41] [Article Influence: 1.8] [Reference Citation Analysis]
534 Nanda I, Zischler H, Epplen C, Guttenbach M, Schmid M. Chromosomal organization of simple repeated DNA sequences used for DNA fingerprinting. Electrophoresis 1991;12:193-203. [PMID: 2040266 DOI: 10.1002/elps.1150120216] [Cited by in Crossref: 29] [Cited by in F6Publishing: 18] [Article Influence: 1.0] [Reference Citation Analysis]
535 Porrini SC, Sciarra A, Sulli N, Piane M, Gualtieri R, Porto GD. Variable Number of Tandem Repeats in Zygosity Diagnosis in Twins. Acta genet med gemellol : twin res 1990;39:473-7. [DOI: 10.1017/s000156600000369x] [Cited by in Crossref: 5] [Article Influence: 0.7] [Reference Citation Analysis]
536 Procaccini G, Olsen JL, Reusch TB. Contribution of genetics and genomics to seagrass biology and conservation. Journal of Experimental Marine Biology and Ecology 2007;350:234-59. [DOI: 10.1016/j.jembe.2007.05.035] [Cited by in Crossref: 110] [Cited by in F6Publishing: 30] [Article Influence: 7.9] [Reference Citation Analysis]
537 Armour JA, Povey S, Jeremiah S, Jeffreys AJ. Systematic cloning of human minisatellites from ordered array charomid libraries. Genomics 1990;8:501-12. [DOI: 10.1016/0888-7543(90)90037-u] [Cited by in Crossref: 97] [Cited by in F6Publishing: 19] [Article Influence: 3.1] [Reference Citation Analysis]
538 Budowle B, Baechtel FS, Comey CT, Giusti AM, Klevan L. Simple protocols for typing forensic biological evidence: Chemiluminescent detection for human DNA quantitation and restriction fragment length polymorphism (RELP) analyses and manual typing of polymerase chain reaction (PCR) amplified polymorphisms. Electrophoresis 1995;16:1559-67. [DOI: 10.1002/elps.11501601259] [Cited by in Crossref: 50] [Cited by in F6Publishing: 19] [Article Influence: 1.9] [Reference Citation Analysis]
539 Keable H, Bourhis J, Brison O, Lehn P, Schenmetzler C, Devergie A, Gluckman E. Long-term study of chimaerism in bone marrow transplantation recipients for severe aplastic anaemia. Br J Haematol 1989;71:525-33. [DOI: 10.1111/j.1365-2141.1989.tb06313.x] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 0.3] [Reference Citation Analysis]
540 Ryan SG. Genetic susceptibility to neurodevelopmental disorders. J Child Neurol 1999;14:187-95. [PMID: 10190270 DOI: 10.1177/088307389901400310] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
541 Signer EN, Gu F, Gustavsson I, Andersson L, Jeffreys AJ. A pseudoautosomal minisatellite in the pig. Mammalian Genome 1994;5:48-51. [DOI: 10.1007/bf00360569] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
542 Weston A, Godbold JH. Polymorphisms of H-ras-1 and p53 in breast cancer and lung cancer: a meta-analysis. Environ Health Perspect 1997;105 Suppl 4:919-26. [PMID: 9255581 DOI: 10.1289/ehp.97105s4919] [Cited by in Crossref: 43] [Cited by in F6Publishing: 40] [Article Influence: 1.8] [Reference Citation Analysis]
543 Mellon CD, Byerley WF. Strategies for linkage studies in schizophrenia. Schizophrenia Research 1989;2:277-85. [DOI: 10.1016/0920-9964(89)90004-2] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.2] [Reference Citation Analysis]
544 Kraemer C, Schmidt ER. The sex determining region of Chironomus thummi is associated with highly repetitive DNA and transposable elements. Chromosoma 1993;102:553-62. [DOI: 10.1007/bf00368348] [Cited by in Crossref: 29] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
545 Epplen JT, Melmer G, Schmidt P, Roewer L, Hundrieser J, Epplen C, Buitkamp J. On the potential of simple repetitive DNA for fingerprinting in clinical, forensic, and evolutionary dynamic studies. Clin Investig 1992;70:1043-51. [PMID: 1472835 DOI: 10.1007/BF00180316] [Cited by in Crossref: 13] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
546 Roberts R, Steer CJ. Disease Genes and Gene Regulation by microRNAs. J of Cardiovasc Trans Res 2010;3:169-72. [DOI: 10.1007/s12265-010-9186-6] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
547 Prindiville T, Cantrell M, Gershwin M. Characterization and Heterogeneity of Monoclonal Antibodies Directed to Intestinal Mucin Derived from Crohn's Disease Small Bowel. Hybridoma 1991;10:269-80. [DOI: 10.1089/hyb.1991.10.269] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
548 Lynch HT, Watson P, Kriegler M, Lynch JF, Lanspa SJ, Marcus J, Smyrk T, Fitzgibbons RJ, Cristofaro G. Differential diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome I and Lynch syndrome II). Dis Colon Rectum. 1988;31:372-377. [PMID: 3366037 DOI: 10.1007/BF02564888] [Cited by in Crossref: 76] [Cited by in F6Publishing: 14] [Article Influence: 2.3] [Reference Citation Analysis]
549 Marino MA, Turni LA, Del Rio SA, Williams PE. Molecular size determinations of DNA restriction fragments and polymerase chain reaction products using capillary gel electrophoresis. Journal of Chromatography A 1994;676:185-9. [DOI: 10.1016/0021-9673(94)80460-5] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 0.4] [Reference Citation Analysis]
550 Shapira MY, Resnick IB, Bitan M, Ackerstein A, Samuel S, Elad S, Miron S, Zilberman I, Slavin S, Or R. Low transplant-related mortality with allogeneic stem cell transplantation in elderly patients. Bone Marrow Transplant 2004;34:155-9. [DOI: 10.1038/sj.bmt.1704540] [Cited by in Crossref: 26] [Cited by in F6Publishing: 19] [Article Influence: 1.5] [Reference Citation Analysis]
551 Byerley W, Mellon C, O'Connell P, Lalouel JM, Nakamura Y, Leppert M, White R. Mapping genes for manic-depression and schizophrenia with DNA markers. Trends Neurosci 1989;12:46-8. [PMID: 2469209 DOI: 10.1016/0166-2236(89)90134-3] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
552 Musarella MA. Gene mapping of ocular diseases. Survey of Ophthalmology 1992;36:285-312. [DOI: 10.1016/0039-6257(92)90096-c] [Cited by in Crossref: 69] [Cited by in F6Publishing: 1] [Article Influence: 2.4] [Reference Citation Analysis]
553 Ahn EK, Kim WJ, Kwon JA, Choi PJ, Kim WJ, Sunwoo Y, Heo J, Leem SH. Variants of MUC5B minisatellites and the susceptibility of bladder cancer. DNA Cell Biol 2009;28:169-76. [PMID: 19191526 DOI: 10.1089/dna.2008.0827] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
554 Thompson EA. 8 Estimation of relationships from genetic data. Statistical Methods in Biological and Medical Sciences. Elsevier; 1991. pp. 255-69. [DOI: 10.1016/s0169-7161(05)80164-6] [Cited by in Crossref: 6] [Article Influence: 0.2] [Reference Citation Analysis]
555 Kaplan J, Hukku B. Chapter 11 Cell Line Characterization and Authentication. Animal Cell Culture Methods. Elsevier; 1998. pp. 203-16. [DOI: 10.1016/s0091-679x(08)61579-4] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
556 Ramel C. Mini- and microsatellites. Environ Health Perspect 1997;105 Suppl 4:781-9. [PMID: 9255562 DOI: 10.1289/ehp.97105s4781] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 0.4] [Reference Citation Analysis]
557 van Haeringen A, Bergman W, Nelen MR, van der Kooij-meijs E, Hendrikse I, Wijnen JT, Khan PM, Klasen EC, Frants RR. Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in dutch families. Genomics 1989;5:61-4. [DOI: 10.1016/0888-7543(89)90086-4] [Cited by in Crossref: 65] [Cited by in F6Publishing: 46] [Article Influence: 2.0] [Reference Citation Analysis]
558 Kim J, Ashworth L, Branscomb E, Stubbs L. The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4. Genome Res 1997;7:532-40. [PMID: 9149948 DOI: 10.1101/gr.7.5.532] [Cited by in Crossref: 84] [Cited by in F6Publishing: 77] [Article Influence: 3.5] [Reference Citation Analysis]
559 Gokool S, Smith D, Curtis C. The use of PCR to help quantify the protection provided by impregnated bednets. Parasitology Today 1992;8:347-50. [DOI: 10.1016/0169-4758(92)90072-a] [Cited by in Crossref: 21] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
560 Boyle JM, Hey Y, Myers K, Stern PL, Grzeschik FH, Ikehara Y, Misumi Y, Fox M. Regional localization of a trophoblast antigen-related sequence and 16 other sequences to human chromosomes 6q using somatic cell hybrids. Genomics 1992;12:693-8. [PMID: 1572643 DOI: 10.1016/0888-7543(92)90296-5] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 0.4] [Reference Citation Analysis]
561 Morling N, Hansen HE. Paternity testing with VNTR DNA systems: I. Matching criteria and population frequencies of the VNTR systems D2S44, D5S43, D7S21, D7S22, and D12S11 in Danes. Int J Leg Med 1993;105:189-96. [DOI: 10.1007/bf01642792] [Cited by in Crossref: 12] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
562 Ince AG, Karaca M, Onus AN. Development and utilization of diagnostic DAMD-PCR markers for Capsicum accessions. Genet Resour Crop Evol 2009;56:211-21. [DOI: 10.1007/s10722-008-9356-4] [Cited by in Crossref: 26] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
563 O'connell P, Lathrop G, Nakamura Y, Leppert M, Lalouel J, White R. Twenty loci form a continuous linkage map of markers for human chromosome 2. Genomics 1989;5:738-45. [DOI: 10.1016/0888-7543(89)90115-8] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 0.6] [Reference Citation Analysis]
564 Shapira MY, Or R, Resnick IB, Bitan M, Ackerstein A, Samuel S, Elad S, Zilberman I, Miron S, Slavin S. A new minimally ablative stem cell transplantation procedure in high-risk patients not eligible for nonmyeloablative allogeneic bone marrow transplantation. Bone Marrow Transplant 2003;32:557-61. [DOI: 10.1038/sj.bmt.1704190] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
565 Skolnick MH, Wallace RB. Simultaneous analysis of multiple polymorphic loci using amplified sequence polymorphisms (ASPs). Genomics 1988;2:273-9. [PMID: 2906038 DOI: 10.1016/0888-7543(88)90014-6] [Cited by in Crossref: 30] [Cited by in F6Publishing: 26] [Article Influence: 0.9] [Reference Citation Analysis]
566 Tremblay J, Hum DH, Sanchez R, Dumas P, Pravenec M, Krenova D, Kren V, Kunes J, Pausova Z, Gossard F, Hamet P. TA repeat variation, Npr1 expression, and blood pressure: impact of the Ace locus. Hypertension 2003;41:16-24. [PMID: 12511524 DOI: 10.1161/01.hyp.0000042664.75193.1b] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 0.9] [Reference Citation Analysis]
567 Nakamura Y, Carlson M, Krapcho K, Gill J, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence pMCK2 on chromosome 10 [D10S15]. Nucleic Acids Res 1988;16:374. [PMID: 2448751 DOI: 10.1093/nar/16.1.374] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 0.3] [Reference Citation Analysis]
568 Macleod RA, Drexler HG. Authentication and Characterization. In: Masters JRW, Palsson BO, editors. Human Cell Culture. Dordrecht: Kluwer Academic Publishers; 2002. pp. 371-97. [DOI: 10.1007/0-306-46877-8_13] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
569 Nickerson DA, Kaiser R, Lappin S, Stewart J, Hood L, Landegren U. Automated DNA diagnostics using an ELISA-based oligonucleotide ligation assay. Proc Natl Acad Sci U S A 1990;87:8923-7. [PMID: 2247466 DOI: 10.1073/pnas.87.22.8923] [Cited by in Crossref: 164] [Cited by in F6Publishing: 130] [Article Influence: 5.5] [Reference Citation Analysis]
570 Costa T, Greer W, Rysiecki G, Buncic JR, Ray PN. Monozygotic twins discordant for Aicardi syndrome. J Med Genet 1997;34:688-91. [PMID: 9279766 DOI: 10.1136/jmg.34.8.688] [Cited by in Crossref: 21] [Cited by in F6Publishing: 13] [Article Influence: 0.9] [Reference Citation Analysis]
571 Jeffreys A. DNA typing: approaches and applications. Journal of the Forensic Science Society 1993;33:204-11. [DOI: 10.1016/s0015-7368(93)73016-9] [Cited by in Crossref: 18] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
572 Slavin S, Nagler A, Naparstek E, Kapelushnik Y, Aker M, Cividalli G, Varadi G, Kirschbaum M, Ackerstein A, Samuel S, Amar A, Brautbar C, Ben-tal O, Eldor A, Or R. Nonmyeloablative Stem Cell Transplantation and Cell Therapy as an Alternative to Conventional Bone Marrow Transplantation With Lethal Cytoreduction for the Treatment of Malignant and Nonmalignant Hematologic Diseases. Blood 1998;91:756-63. [DOI: 10.1182/blood.v91.3.756.756_756_763] [Cited by in Crossref: 18] [Article Influence: 0.8] [Reference Citation Analysis]
573 Xiong F, Liu J, Jiang J, Zhong R, He L, Han Z, Li Z, Tang X, Tang R. Molecular profiling of genetic variability in domesticated groundnut (Arachis hypogaea L.) based on ISJ, URP, and DAMD markers. Biochem Genet 2013;51:889-900. [PMID: 23835917 DOI: 10.1007/s10528-013-9615-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
574 Nakamura Y, Martin C, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence pYNM3 on chromosome 8 (D8S38). Nucleic Acids Res 1987;15:10080. [PMID: 2892174 DOI: 10.1093/nar/15.23.10080] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
575 Rassmann K, Schlötterer C, Tautz D. Isolation of simple-sequence loci for use in polymerase chain reaction-based DNA fingerprinting. Electrophoresis 1991;12:113-8. [DOI: 10.1002/elps.1150120205] [Cited by in Crossref: 141] [Cited by in F6Publishing: 78] [Article Influence: 4.7] [Reference Citation Analysis]
576 Westneat DF, Webster MS. Molecular analysis of kinship in birds: Interesting questions and useful techniques. In: Schierwater B, Streit B, Wagner GP, Desalle R, editors. Molecular Ecology and Evolution: Approaches and Applications. Basel: Birkhäuser; 1994. pp. 91-126. [DOI: 10.1007/978-3-0348-7527-1_7] [Cited by in Crossref: 42] [Cited by in F6Publishing: 18] [Article Influence: 1.6] [Reference Citation Analysis]
577 Sinnett D, Deragon J, Simard LR, Labuda D. Alumorphs—Human DNA polymorphisms detected by polymerase chain reaction using Alu-specific primers. Genomics 1990;7:331-4. [DOI: 10.1016/0888-7543(90)90166-r] [Cited by in Crossref: 41] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
578 Lundwall A. The Structure of the Semenogelin Gene Locus. Nucleotide Sequence of the Intergenic and the Flanking DNA. Eur J Biochem 1996;235:466-70. [DOI: 10.1111/j.1432-1033.1996.00466.x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.2] [Reference Citation Analysis]
579 St. Clair DM, St. Clair JB, Swainson CP, Bamforth F, Machin GA. Twin zygosity testing for medical purposes. Am J Med Genet 1998;77:412-4. [DOI: 10.1002/(sici)1096-8628(19980605)77:5<412::aid-ajmg11>3.0.co;2-l] [Cited by in Crossref: 27] [Cited by in F6Publishing: 1] [Article Influence: 1.2] [Reference Citation Analysis]
580 . Spontaneous mutation at the hypervariable mouse minisatellite locus Ms6-hm : flanking DNA sequence and analysis of germline and early somatic mutation events. Proc R Soc Lond B 1997;245:235-45. [DOI: 10.1098/rspb.1991.0115] [Cited by in Crossref: 34] [Cited by in F6Publishing: 31] [Article Influence: 1.4] [Reference Citation Analysis]
581 Cooper DN, Clayton JF. DNA polymorphism and the study of disease associations. Hum Genet 1988;78:299-312. [PMID: 2896152 DOI: 10.1007/BF00291724] [Cited by in Crossref: 65] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
582 Imyanitov EN, Chernitsa OI, Nikiforova IF. Loss of heterozygosity at chromosome 17p is associated with HER-2 amplification and lack of nodal involvement in breast cancer. Int J Cancer 1993;53:11-6. [DOI: 10.1002/ijc.2910530104] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 0.3] [Reference Citation Analysis]
583 Häne BG, Jäger K, Drexler HG. The Pearson product-moment correlation coefficient is better suited for identification of DNA fingerprint profiles than band matching algorithms. Electrophoresis 1993;14:967-72. [PMID: 8125064 DOI: 10.1002/elps.11501401154] [Cited by in Crossref: 130] [Cited by in F6Publishing: 92] [Article Influence: 4.8] [Reference Citation Analysis]
584 Pergolizzi RG, Erster SH. Analysis of chromosome 22 loci in meningioma: Alterations in the leukemia inhibitory factor (LIF) locus. Molecular and Chemical Neuropathology 1994;21:189-217. [DOI: 10.1007/bf02815351] [Cited by in Crossref: 8] [Article Influence: 0.3] [Reference Citation Analysis]
585 Orrego C, King MC. DETERMINATION OF FAMILIAL RELATIONSHIPS. PCR Protocols. Elsevier; 1990. pp. 416-26. [DOI: 10.1016/b978-0-12-372180-8.50054-8] [Cited by in Crossref: 16] [Article Influence: 0.5] [Reference Citation Analysis]
586 Jurka J. Approaches to Identification and Analysis of Interspersed Repetitive DNA Sequences. Automated DNA Sequencing and Analysis. Elsevier; 1994. pp. 294-8. [DOI: 10.1016/b978-0-08-092639-1.50043-5] [Cited by in Crossref: 10] [Article Influence: 0.4] [Reference Citation Analysis]
587 Cederberg H, Agurell E, Hedenskog M, Rannug U. Amplification and loss of repeat units of the human minisatellite MS1 integrated in chromosome III of a haploid yeast strain. Mol Gen Genet 1993;238:38-42. [PMID: 8479438 DOI: 10.1007/BF00279528] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
588 Bikker H, Baas F, de Vijlder J. Structure and characterization of a 50 bp repeat in intron 10 of the human thyroid peroxidase gene. Molecular and Cellular Endocrinology 1992;83:21-8. [DOI: 10.1016/0303-7207(92)90191-8] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
589 Gottlieb J, Muzyczka N. In vitro excision of adeno-associated virus DNA from recombinant plasmids: isolation of an enzyme fraction from HeLa cells that cleaves DNA at poly(G) sequences. Mol Cell Biol 1988;8:2513-22. [PMID: 2841582 DOI: 10.1128/mcb.8.6.2513-2522.1988] [Cited by in Crossref: 1] [Cited by in F6Publishing: 7] [Article Influence: 0.0] [Reference Citation Analysis]
590 Ravel C, Wincker P, Bastien P, Blaineau C, Pagès M. A polymorphic minisatellite sequence in the subtelomeric regions of chromosomes I and V in Leishmania infantum. Molecular and Biochemical Parasitology 1995;74:31-41. [DOI: 10.1016/0166-6851(95)02480-8] [Cited by in Crossref: 20] [Cited by in F6Publishing: 23] [Article Influence: 0.8] [Reference Citation Analysis]
591 Ip NY, Nicholas L, Baum H, Balazs I. Discovery of a novel multilocus DNA polymorphism [DNF24]. Nucleic Acids Res 1989;17:4427. [PMID: 2567990 DOI: 10.1093/nar/17.11.4427] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
592 Culver HR, Sinha J, Prieto TR, Calo CJ, Fairbanks BD, Bowman CN. Click Nucleic Acid–DNA Binding Behavior: Dependence on Length, Sequence, and Ionic Strength. Biomacromolecules 2020;21:4205-11. [DOI: 10.1021/acs.biomac.0c00996] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
593 Cooper DN, Hall C. Down's syndrome and the molecular biology of chromosome 21. Progress in Neurobiology 1988;30:507-30. [DOI: 10.1016/0301-0082(88)90033-0] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 0.6] [Reference Citation Analysis]
594 Allingham-Hawkins DJ, Tomkins DJ. Heterogeneity in Roberts syndrome. Am J Med Genet 1995;55:188-94. [PMID: 7536395 DOI: 10.1002/ajmg.1320550208] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
595 Weller J, Kashi Y, Soller M. Power of Daughter and Granddaughter Designs for Determining Linkage Between Marker Loci and Quantitative Trait Loci in Dairy Cattle. Journal of Dairy Science 1990;73:2525-37. [DOI: 10.3168/jds.s0022-0302(90)78938-2] [Cited by in Crossref: 255] [Cited by in F6Publishing: 28] [Article Influence: 8.2] [Reference Citation Analysis]
596 Abdul-Muneer PM. Application of microsatellite markers in conservation genetics and fisheries management: recent advances in population structure analysis and conservation strategies. Genet Res Int 2014;2014:691759. [PMID: 24808959 DOI: 10.1155/2014/691759] [Cited by in Crossref: 70] [Cited by in F6Publishing: 27] [Article Influence: 10.0] [Reference Citation Analysis]
597 Berman E, Jhanwar S, Mcbride M, Strife A, Wisniewski D, Lambek C, Clarkson B. Characterization of two novel sublines established from a human megakaryoblastic leukemia cell line transfected with p210BCR-ABL. Leukemia Research 2000;24:289-97. [DOI: 10.1016/s0145-2126(99)00179-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
598 Zhu ZB, Hsieh SL, Bentley DR, Campbell RD, Volanakis JE. A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus. J Exp Med 1992;175:1783-7. [PMID: 1350302 DOI: 10.1084/jem.175.6.1783] [Cited by in Crossref: 44] [Cited by in F6Publishing: 37] [Article Influence: 1.5] [Reference Citation Analysis]
599 Batzer MA, Gudi VA, Mena JC, Foltz DW, Herrera RJ, Deininger PL. Amplification dynamics of human-specific (HS) Alu family members. Nucleic Acids Res 1991;19:3619-23. [PMID: 1649453 DOI: 10.1093/nar/19.13.3619] [Cited by in Crossref: 70] [Cited by in F6Publishing: 74] [Article Influence: 2.3] [Reference Citation Analysis]
600 Laing CR, Zhang Y, Thomas JE, Gannon VP. Everything at once: comparative analysis of the genomes of bacterial pathogens. Vet Microbiol 2011;153:13-26. [PMID: 21764529 DOI: 10.1016/j.vetmic.2011.06.014] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.8] [Reference Citation Analysis]
601 Hunt JD, Tereba A. Molecular evaluation of abnormalities of the short arm of chromosome I in neuroblastoma. Genes Chromosom Cancer 1990;2:137-46. [DOI: 10.1002/gcc.2870020210] [Cited by in Crossref: 26] [Cited by in F6Publishing: 24] [Article Influence: 0.8] [Reference Citation Analysis]
602 Skowasch K, Wiegand P, Brinkmann B. pMCT 118 (D1S80): a new allelic ladder and an improved electrophoretic separation lead to the demonstration of 28 alleles. Int J Leg Med 1992;105:165-8. [DOI: 10.1007/bf01625170] [Cited by in Crossref: 34] [Article Influence: 1.2] [Reference Citation Analysis]
603 Shin E, Fujita S, Takami K, Kurahashi H, Kurita Y, Kobayashi T, Mori T, Nishisho I, Takai S. Deletion Mapping of Chromosome 1p and 22q in Pheochromocytoma. Japanese Journal of Cancer Research 1993;84:402-8. [DOI: 10.1111/j.1349-7006.1993.tb00150.x] [Cited by in Crossref: 28] [Cited by in F6Publishing: 26] [Article Influence: 1.0] [Reference Citation Analysis]
604 Chen WJ, Faraone SV, Tsuang MT, Vogler GP. Linkage studies of schizophrenia: A simulation study of statistical power: Power of Schizophrenia Linkage Studies. Genet Epidemiol 1992;9:123-39. [DOI: 10.1002/gepi.1370090205] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 1.3] [Reference Citation Analysis]
605 Tang H, Nzabarushimana E. STRScan: targeted profiling of short tandem repeats in whole-genome sequencing data. BMC Bioinformatics 2017;18:398. [PMID: 28984185 DOI: 10.1186/s12859-017-1800-z] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
606 Brookes AJ, Hedge PH, Solomon E. A highly polymorphic locus on chromosome 11 which has homology to a collagen triple-helix coding sequence. Nucleic Acids Res 1989;17:1792. [PMID: 2564196 DOI: 10.1093/nar/17.4.1792] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
607 Nakamura Y, Culver M, Sergeant L, Leppert M, O'Connell P, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57]. Nucleic Acids Res 1988;16:4747. [PMID: 2454462 DOI: 10.1093/nar/16.10.4747] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 0.5] [Reference Citation Analysis]
608 Fowler SJ, Gill P, Werrett DJ, Higgs DR. Individual specific DNA fingerprints from a hypervariable region probe: alpha-globin 3'HVR. Hum Genet 1988;79:142-6. [PMID: 3164703 DOI: 10.1007/BF00280553] [Cited by in Crossref: 45] [Cited by in F6Publishing: 5] [Article Influence: 1.4] [Reference Citation Analysis]
609 Turner BJ, Elder JF, Lauchlin TF. Repetitive DNA sequences and the divergence offish populations: some hopeful beginnings. Journal of Fish Biology 1991;39:131-42. [DOI: 10.1111/j.1095-8649.1991.tb05077.x] [Cited by in Crossref: 17] [Cited by in F6Publishing: 7] [Article Influence: 1.1] [Reference Citation Analysis]
610 Katju V. In with the old, in with the new: the promiscuity of the duplication process engenders diverse pathways for novel gene creation. Int J Evol Biol 2012;2012:341932. [PMID: 23008799 DOI: 10.1155/2012/341932] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 2.7] [Reference Citation Analysis]
611 Wreschner DH, Tsarfaty I, Hareuveni M, Zaretsky J, Smorodinsky N, Weiss M, Horev J, Kotkes P, Zrihan S, Jeltsch JM, Green S, Lathe R, Keydar I. Isolation and Characterization of Full Length cDNA Coding for the H23 Breast Tumor Associated Antigen. In: Rich MA, Hager JC, Keydar I, editors. Breast Cancer: Progress in Biology, Clinical Management and Prevention. Boston: Springer US; 1989. pp. 41-59. [DOI: 10.1007/978-1-4613-1617-6_4] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.2] [Reference Citation Analysis]
612 Morin PA, Wallis J, Moore JJ, Woodruff DS. Paternity exclusion in a community of wild chimpanzees using hypervariable simple sequence repeats. Mol Ecol 1994;3:469-77. [PMID: 7952327 DOI: 10.1111/j.1365-294x.1994.tb00125.x] [Cited by in Crossref: 81] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
613 Armour JA, Crosier M, Jeffreys AJ. Human minisatellite alleles detectable only after PCR amplification. Genomics 1992;12:116-24. [DOI: 10.1016/0888-7543(92)90413-m] [Cited by in Crossref: 12] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
614 Kashi Y, Iraqi F, Tikochinski Y, Ruzitsky B, Nave A, Beckmann JS, Friedmann A, Soller M, Gruenbaum Y. (TG)n uncovers a sex-specific hybridization pattern in cattle. Genomics 1990;7:31-6. [DOI: 10.1016/0888-7543(90)90515-v] [Cited by in Crossref: 23] [Article Influence: 0.7] [Reference Citation Analysis]
615 Dracopoli NC, O'connell P, Elsner TI, Lalouel J, White RL, Buetow KH, Nishimura DY, Murray JC, Helms C, Mishra SK, Donis-keller H, Hall JM, Lee MK, King M, Attwood J, Morton NE, Robson EB, Mahtani M, Willard HF, Royle NJ, Patel I, Jeffreys AJ, Verga V, Jenkins T, Weber JL, Mitchell AL, Bale AE. The CEPH consortium linkage map of human chromosome 1. Genomics 1991;9:686-700. [DOI: 10.1016/0888-7543(91)90362-i] [Cited by in Crossref: 74] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
616 Andersson B, Lu F, Muzny DM, Warren ST, Gibbs RA. Complete sequence of a 38.4-kb human cosmid insert containing the polymorphic marker DXS455 from Xq28. DNA Sequence 2009;5:219-23. [DOI: 10.3109/10425179509030969] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
617 Alers JC, van Dekken H. Interphase Cytogenetic Analysis of Solid Tumors by Non-Isotopic DNA in situ Hybridization. Progress in Histochemistry and Cytochemistry 1996;31:III-133. [DOI: 10.1016/s0079-6336(96)80017-9] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
618 Ward RD, Grewe PM. Appraisal of molecular genetic techniques in fisheries. Rev Fish Biol Fisheries 1994;4:300-25. [DOI: 10.1007/bf00042907] [Cited by in Crossref: 82] [Article Influence: 3.0] [Reference Citation Analysis]
619 Pepe G. A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta. Hum Mutat 1993;2:300-5. [DOI: 10.1002/humu.1380020410] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 0.6] [Reference Citation Analysis]
620 Moyzis RK, Torney DC, Meyne J, Buckingham JM, Wu JR, Burks C, Sirotkin KM, Goad WB. The distribution of interspersed repetitive DNA sequences in the human genome. Genomics 1989;4:273-89. [PMID: 2714792 DOI: 10.1016/0888-7543(89)90331-5] [Cited by in Crossref: 127] [Cited by in F6Publishing: 115] [Article Influence: 4.0] [Reference Citation Analysis]
621 Yokoi T, Sagisaka K. Haptoglobin typing of human bloodstains using a specific DNA probe. Forensic Science International 1990;45:39-46. [DOI: 10.1016/0379-0738(90)90219-o] [Cited by in Crossref: 8] [Article Influence: 0.3] [Reference Citation Analysis]
622 Chung RY, Seizinger BR. Tumor Suppressor Genes and Cancer of the Human Nervous System. Cancer Investigation 2009;9:429-38. [DOI: 10.3109/07357909109084641] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 1.1] [Reference Citation Analysis]
623 Ito I, Yoshimoto M, Iwase T, Watanabe S, Katagiri T, Harada Y, Kasumi F, Yasuda S, Mitomi T, Emi M. Association of genetic alterations on chromosome 17 and loss of hormone receptors in breast cancer. Br J Cancer 1995;71:438-41. [PMID: 7880720 DOI: 10.1038/bjc.1995.89] [Cited by in Crossref: 33] [Cited by in F6Publishing: 30] [Article Influence: 1.3] [Reference Citation Analysis]
624 Hong Y, Chuah A. A format for databasing and comparison of AFLP fingerprint profiles. BMC Bioinformatics 2003;4:7. [PMID: 12600280 DOI: 10.1186/1471-2105-4-7] [Cited by in Crossref: 14] [Cited by in F6Publishing: 8] [Article Influence: 0.8] [Reference Citation Analysis]
625 Takita K, Tanigami A, Tokino T, Jones C, Nakamura Y. Identification of 57 conventional RFLP and 6 VNTR systems with 32 DNA clones on chromosome 11p15. Genomics 1992;13:1296-9. [DOI: 10.1016/0888-7543(92)90049-x] [Cited by in Crossref: 3] [Article Influence: 0.1] [Reference Citation Analysis]
626 Batzer MA, Deininger PL. Alu repeats and human genomic diversity. Nat Rev Genet 2002;3:370-9. [DOI: 10.1038/nrg798] [Cited by in Crossref: 883] [Cited by in F6Publishing: 747] [Article Influence: 46.5] [Reference Citation Analysis]
627 Buetow KH, Murray JC, Israel JL, London WT, Smith M, Kew M, Blanquet V, Brechot C, Redeker A, Govindarajah S. Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proc Natl Acad Sci U S A 1989;86:8852-6. [PMID: 2573067 DOI: 10.1073/pnas.86.22.8852] [Cited by in Crossref: 132] [Cited by in F6Publishing: 131] [Article Influence: 4.1] [Reference Citation Analysis]
628 Korenberg JR, Kalousek DK, Anneren G, Pulst SM, Hall JG, Epstein CJ, Cox DR. Deletion of chromosome 21 and normal intelligence: molecular definition of the lesion. Hum Genet 1991;87:112-8. [PMID: 2066097 DOI: 10.1007/BF00204163] [Cited by in Crossref: 34] [Cited by in F6Publishing: 13] [Article Influence: 1.1] [Reference Citation Analysis]
629 Sala A, Penacino G, Carnese R, Corach D. Reference database of hypervariable genetic markers of Argentina: Application for molecular anthropology and forensic casework. Electrophoresis 1999;20:1733-9. [DOI: 10.1002/(sici)1522-2683(19990101)20:8<1733::aid-elps1733>3.0.co;2-x] [Cited by in Crossref: 24] [Cited by in F6Publishing: 6] [Article Influence: 1.1] [Reference Citation Analysis]
630 Fredholm M, Winterø AK. Efficient resolution of parentage in dogs by amplification of microsatellites. Animal Genetics 1996;27:19-23. [DOI: 10.1111/j.1365-2052.1996.tb01172.x] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
631 Yamamoto S, Sippel KC, Berson EL, Dryja TP. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness. Nat Genet 1997;15:175-8. [DOI: 10.1038/ng0297-175] [Cited by in Crossref: 185] [Cited by in F6Publishing: 138] [Article Influence: 7.7] [Reference Citation Analysis]
632 Julier C, de Gouyon B, Georges M, Guénet JL, Nakamura Y, Avner P, Lathrop GM. Minisatellite linkage maps in the mouse by cross-hybridization with human probes containing tandem repeats. Proc Natl Acad Sci U S A 1990;87:4585-9. [PMID: 2352937 DOI: 10.1073/pnas.87.12.4585] [Cited by in Crossref: 40] [Cited by in F6Publishing: 32] [Article Influence: 1.3] [Reference Citation Analysis]
633 Petros JA, Baumann AK, Ruiz-Pesini E, Amin MB, Sun CQ, Hall J, Lim S, Issa MM, Flanders WD, Hosseini SH. mtDNA mutations increase tumorigenicity in prostate cancer. Proc Natl Acad Sci USA. 2005;102:719-724. [PMID: 15647368 DOI: 10.1073/pnas.0408894102] [Cited by in Crossref: 565] [Cited by in F6Publishing: 515] [Article Influence: 35.3] [Reference Citation Analysis]
634 Boldyreff B, Wehr K, Hecht R, Issinger O. Identification of four genomic loci highly related to caseinkinase-2-α cDNA and characterization of a casein kinase-2-α pseudogene within the mouse genome. Biochemical and Biophysical Research Communications 1992;186:723-30. [DOI: 10.1016/0006-291x(92)90806-v] [Cited by in Crossref: 5] [Article Influence: 0.2] [Reference Citation Analysis]
635 Effert PJ, Neubauer A, Walther PJ, Liu ET. Alterations of The P53 Gene Are Associated With The Progression Of A Human Prostate Carcinoma. Journal of Urology 1992;147:789-93. [DOI: 10.1016/s0022-5347(17)37387-1] [Cited by in Crossref: 75] [Cited by in F6Publishing: 13] [Article Influence: 2.6] [Reference Citation Analysis]
636 Caspary WJ, Stopper H, Hozier JC, Liechty MC, Davis LM. Mechanisms Leading to the Expression of Recessive Alleles: The Use of Polymorphic Microsatellites and Whole-Chromosome Painting Probes to Analyze Mouse Tumors, Mutants, and Micronuclei. In: Müller-hermelink HK, Neumann H, Dekant W, editors. Risk and Progression Factors in Carcinogenesis. Berlin: Springer Berlin Heidelberg; 1997. pp. 161-82. [DOI: 10.1007/978-3-642-60393-8_11] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
637 Akpinar E, Keary JM, Kurlander R, Hale DA. Measurement of chimerism in cynomolgus monkeys using human-specific short tandem repeat-based assay. Transplantation 2005;79:236-9. [PMID: 15665773 DOI: 10.1097/01.tp.0000148916.95656.93] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
638 Tsuge M, Hamamoto R, Silva FP, Ohnishi Y, Chayama K, Kamatani N, Furukawa Y, Nakamura Y. A variable number of tandem repeats polymorphism in an E2F-1 binding element in the 5' flanking region of SMYD3 is a risk factor for human cancers. Nat Genet. 2005;37:1104-1107. [PMID: 16155568 DOI: 10.1038/ng1638] [Cited by in Crossref: 85] [Cited by in F6Publishing: 77] [Article Influence: 5.3] [Reference Citation Analysis]
639 Weber B, Collins C, Kowbel D, Riess O, Hayden MR. Identification of multiple CpG islands and associated conserved sequences in a candidate region for the Huntington disease gene. Genomics 1991;11:1113-24. [PMID: 1838348 DOI: 10.1016/0888-7543(91)90039-h] [Cited by in Crossref: 16] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
640 Vuorio AF, Sajantila A, Hämäläinen T, Syvänen A, Ehnholm C, Peltonen L. Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems. Biochemical and Biophysical Research Communications 1990;170:616-20. [DOI: 10.1016/0006-291x(90)92136-n] [Cited by in Crossref: 18] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
641 Farag SS, Wood LL, Schwartz JE, Srivastava S, Nelson RP, Robertson MJ, Abonour R, Secrest A, Cox E, Baute J. Phase I trial and pharmacokinetic study of high-dose clofarabine and busulfan and allogeneic stem cell transplantation in adults with high-risk and refractory acute leukemia. Leukemia. 2011;25:599-605. [PMID: 21252987 DOI: 10.1038/leu.2010.319] [Cited by in Crossref: 29] [Cited by in F6Publishing: 26] [Article Influence: 2.9] [Reference Citation Analysis]
642 Prodöhl PA, Taggart JB, Ferguson A. Single locus inheritance and joint segregation analysis of minisatellite (VNTR) DNA loci in brown trout (Salmo trutta L.). Heredity 1994;73:556-66. [DOI: 10.1038/hdy.1994.155] [Cited by in Crossref: 28] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
643 Plass C, Hellwig T, Traut W, Winking H. Evolution of a B2 tagged sequence from a long-range repeat family in the genus Mus. Mammalian Genome 1992;3:197-201. [DOI: 10.1007/bf00355719] [Cited by in Crossref: 5] [Article Influence: 0.2] [Reference Citation Analysis]
644 Van Roy N, Laureys G, Cheng NC, Willem P, Opedenakker G, Versteeg R, Speleman F. I;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines. Genes Chromosom Cancer 1994;10:103-14. [DOI: 10.1002/gcc.2870100205] [Cited by in Crossref: 114] [Cited by in F6Publishing: 103] [Article Influence: 4.2] [Reference Citation Analysis]
645 Goodfellow PN. Human genome project. Variation is now the theme. Nature 1992;359:777-8. [PMID: 1359422 DOI: 10.1038/359777a0] [Cited by in Crossref: 14] [Cited by in F6Publishing: 7] [Article Influence: 0.5] [Reference Citation Analysis]
646 Nakamura Y, Lathrop M, O'connell P, Leppert M, Lalouel J, White R. A primary map of ten DNA markers and two serological markers for human chromosome 19. Genomics 1988;3:67-71. [DOI: 10.1016/0888-7543(88)90161-9] [Cited by in Crossref: 47] [Cited by in F6Publishing: 42] [Article Influence: 1.4] [Reference Citation Analysis]
647 Kim YS, Kim MH, Choi YK, Kim C, Lee D. Allelic divergence in the human insulin gene provides evidence for intragenic recombination events in the non-coding regions: evidence for existence of new alleles. Molec Gen Genet 1994;245:146-51. [DOI: 10.1007/bf00283261] [Cited by in Crossref: 4] [Article Influence: 0.1] [Reference Citation Analysis]
648 Nakamura Y. The Japan Society of Human Genetics Award Lecture. Application of DNA markers to clinical genetics. Jpn J Hum Genet 1996;41:1-10. [PMID: 8914629 DOI: 10.1007/BF01892620] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
649 Järvelä I, Rapola J, Peltonen L, Puhakka L, Vesa J, Ämmälä P, Salonen R, Ryynänen M, Haring P, Mustonen A, Santavuori P. DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1). Prenat Diagn 1991;11:323-8. [DOI: 10.1002/pd.1970110508] [Cited by in Crossref: 23] [Cited by in F6Publishing: 17] [Article Influence: 0.8] [Reference Citation Analysis]
650 Monckton DG, Jeffreys AJ. Minisatellite "isoallele" discrimination in pseudohomozygotes by single molecule PCR and variant repeat mapping. Genomics 1991;11:465-7. [PMID: 1769661 DOI: 10.1016/0888-7543(91)90158-b] [Cited by in Crossref: 10] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
651 Nakamura Y, Martin C, Myers R, White R. Isolation and mapping of a polymorphic DNA sequence (pCMM12) on chromosome 1p [D1S76]. Nucleic Acids Res 1988;16:9368. [PMID: 2902595 DOI: 10.1093/nar/16.19.9368] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
652 Féral J. How useful are the genetic markers in attempts to understand and manage marine biodiversity? Journal of Experimental Marine Biology and Ecology 2002;268:121-45. [DOI: 10.1016/s0022-0981(01)00382-3] [Cited by in Crossref: 102] [Article Influence: 5.4] [Reference Citation Analysis]
653 Watanabe Y, Sakazume T, Kurosaki K, Oota H, Washio-watanabe K, Ueda S. Short tandem repeat polymorphisms in Japanese macaques: Their short repeat lengths and low informativ eness. Mammalian Genome 1996;7:383-5. [DOI: 10.1007/s003359900110] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
654 Kunieda T, Kobayashi E, Tachibana M, Ikadai H, Imamichi T. Polymorphic microsatellite loci of the rat (Rattus norvegicus). Mammalian Genome 1992;3:564-7. [DOI: 10.1007/bf00350622] [Cited by in Crossref: 19] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
655 Amundson SA, Liber HL. A comparison of induced mutation at homologous alleles of the tk locus in human cells. II. Molecular analysis of mutants. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 1992;267:89-95. [DOI: 10.1016/0027-5107(92)90113-g] [Cited by in Crossref: 26] [Cited by in F6Publishing: 4] [Article Influence: 0.9] [Reference Citation Analysis]
656 Spotila LD, Rekosh DM, Loverde PT. Polymorphic repeated DNA element in the genome of Schistosoma mansoni. Molecular and Biochemical Parasitology 1991;48:117-20. [DOI: 10.1016/0166-6851(91)90172-3] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 0.7] [Reference Citation Analysis]
657 Steel CM. Tracing disease genes through family studies. J Pathol 1990;162:7-13. [DOI: 10.1002/path.1711620104] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
658 Farrar G, Mcwilliam P, Sharp EM, Kenna P, Bradley DG, Humphries MM, Mcconnell DJ, Humphries P. Autosomal dominant retinitis pigmentosa: Exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21. Genomics 1989;5:612-8. [DOI: 10.1016/0888-7543(89)90030-x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
659 Huey B, Hall J. Hypervariable DNA fingerprinting in Escherichia coli: minisatellite probe from bacteriophage M13. J Bacteriol 1989;171:2528-32. [PMID: 2565332 DOI: 10.1128/jb.171.5.2528-2532.1989] [Cited by in Crossref: 188] [Cited by in F6Publishing: 137] [Article Influence: 5.9] [Reference Citation Analysis]
660 Rossiter BJF, Thomas Caskey C. Impact of the human genome project on medical practice. Annals of Surgical Oncology 1995;2:14-25. [DOI: 10.1007/bf02303697] [Cited by in Crossref: 2] [Article Influence: 0.1] [Reference Citation Analysis]
661 Economou EP, Bergen AW, Warren AC, Antonarakis SE. The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome. Proc Natl Acad Sci U S A 1990;87:2951-4. [PMID: 2326257 DOI: 10.1073/pnas.87.8.2951] [Cited by in Crossref: 126] [Cited by in F6Publishing: 119] [Article Influence: 4.1] [Reference Citation Analysis]
662 Machin G, Bamforth F, Innes M, Mcnichol K. Some perinatal characteristics of monozygotic twins who are dichorionic. Am J Med Genet 1995;55:71-6. [DOI: 10.1002/ajmg.1320550119] [Cited by in Crossref: 41] [Cited by in F6Publishing: 35] [Article Influence: 1.6] [Reference Citation Analysis]
663 Batzer MA, Deininger PL. A human-specific subfamily of Alu sequences. Genomics 1991;9:481-7. [PMID: 1851725 DOI: 10.1016/0888-7543(91)90414-a] [Cited by in Crossref: 165] [Cited by in F6Publishing: 59] [Article Influence: 5.5] [Reference Citation Analysis]
664 Yamazaki H, Nomoto S, Mishima Y, Kominami R. A 35-kDa protein binding to a cytosine-rich strand of hypervariable minisatellite DNA. Journal of Biological Chemistry 1992;267:12311-6. [DOI: 10.1016/s0021-9258(19)49840-2] [Cited by in Crossref: 16] [Article Influence: 0.6] [Reference Citation Analysis]
665 Christiano AM, Uitto J. Polymorphism of the Human Genome: Markers for Genetic Linkage Analyses in Heritable Diseases of the Skin. Journal of Investigative Dermatology 1992;99:519-23. [DOI: 10.1111/1523-1747.ep12658054] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
666 Mottes M, Cugola L, Cappello N, Pignatti PF. Segregation analysis of dominant osteogenesis imperfecta in Italy. J Med Genet 1990;27:367-70. [PMID: 1972760 DOI: 10.1136/jmg.27.6.367] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
667 Schattenberg A, Bär B, Vet J, Dijk BV, Smeets D, Witte TD. Comparison of Chimerism of Red Cells with that of Granulocytes, T-Lymphocytes, and Bone Marrow Cells in Recipients of Bone Marrow Grafts Depleted of Lymphocytes Using Counterflow Centrifugation. Leukemia & Lymphoma 2009;5:171-7. [DOI: 10.3109/10428199109068122] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
668 den Bakker HC, Gravendeel B, Kuyper TW. An ITS phylogeny of Leccinum and an analysis of the evolution of minisatellite-like sequences within ITS1. Mycologia 2017;96:102-18. [DOI: 10.1080/15572536.2005.11833001] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
669 Chan L. The apolipoprotein multigene family: structure, expression, evolution, and molecular genetics. Klin Wochenschr 1989;67:225-37. [PMID: 2648060 DOI: 10.1007/BF01717324] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
670 Kanai Y, Hui A, Sun L, Ushijima S, Sakamoto M, Tsuda H, Hirohashi S. DNA hypermethylation at the D17S5 locus and reducedHIC-1mRNA expression are associated with hepatocarcinogenesis. Hepatology 1999;29:703-9. [DOI: 10.1002/hep.510290338] [Cited by in Crossref: 78] [Cited by in F6Publishing: 68] [Article Influence: 3.5] [Reference Citation Analysis]
671 Nakamura Y, Martin C, Krapcho K, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (pCMM65) on chromosome 16 [D16S84]. Nucleic Acids Res 1988;16:3122. [PMID: 2897115 DOI: 10.1093/nar/16.7.3122] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 0.3] [Reference Citation Analysis]
672 Oberacher H. On the use of different mass spectrometric techniques for characterization of sequence variability in genomic DNA. Anal Bioanal Chem 2008;391:135-49. [DOI: 10.1007/s00216-008-1929-8] [Cited by in Crossref: 29] [Cited by in F6Publishing: 22] [Article Influence: 2.2] [Reference Citation Analysis]
673 Nagaraju JG, Singh L. Assessment of genetic diversity by DNA profiling and its significance in silkworm, Bombyx mori. Electrophoresis 1997;18:1676-81. [PMID: 9378144 DOI: 10.1002/elps.1150180935] [Cited by in Crossref: 12] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
674 Vergnaud G. Polymers of random short oligonucleotides detect polymorphic loci in the human genome. Nucleic Acids Res 1989;17:7623-30. [PMID: 2798120 DOI: 10.1093/nar/17.19.7623] [Cited by in Crossref: 51] [Cited by in F6Publishing: 38] [Article Influence: 1.6] [Reference Citation Analysis]
675 Weston A, Vineis P, Caporaso NE, Krontiris TG, Lonergan JA, Sugimura H. Racial variation in the distribution of Ha-ras-1 alleles. Mol Carcinog 1991;4:265-8. [DOI: 10.1002/mc.2940040404] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 0.5] [Reference Citation Analysis]
676 Watanabe M, Kondo I, Nissato S, Wakisaka A, Toda T, Ikeda J, Wasmuth JJ, Gusella JF, Kanazawa I. A linkage study with DNA markers (D4S95, D4S115, and D4S111) in Japanese Huntington disease families. Jpn J Hum Genet 1993;38:193-201. [PMID: 8102909 DOI: 10.1007/BF01883710] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
677 Mariat D, Vergnaud G. Detection of polymorphic loci in complex genomes with synthetic tandem repeats. Genomics 1992;12:454-8. [DOI: 10.1016/0888-7543(92)90434-t] [Cited by in Crossref: 14] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
678 Ely J, Deka R, Chakraborty R, Ferrell RE. Comparison of five tandem repeat loci between humans and chimpanzees. Genomics 1992;14:692-8. [DOI: 10.1016/s0888-7543(05)80170-3] [Cited by in Crossref: 12] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
679 Trommelen GJ, Den Daas NH, Vijg J, Uitterlinden AG. Identity and Paternity Testing of Cattle: Application of a Deoxyribonucleic Acid Profiling Protocol. Journal of Dairy Science 1993;76:1403-11. [DOI: 10.3168/jds.s0022-0302(93)77471-8] [Cited by in Crossref: 9] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
680 . The role of cloned genes in the prevention of genetic disease. Phil Trans R Soc Lond B 1988;319:249-61. [DOI: 10.1098/rstb.1988.0047] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
681 Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, Friedman LH, Daiger SP. Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics 1991;11:857-69. [DOI: 10.1016/0888-7543(91)90008-3] [Cited by in Crossref: 127] [Cited by in F6Publishing: 84] [Article Influence: 4.2] [Reference Citation Analysis]
682 Armour JA, Wong Z, Wilson V, Royle NJ, Jeffreys AJ. Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements. Nucleic Acids Res 1989;17:4925-35. [PMID: 2762114 DOI: 10.1093/nar/17.13.4925] [Cited by in Crossref: 72] [Cited by in F6Publishing: 70] [Article Influence: 2.3] [Reference Citation Analysis]
683 Wong Z, Royle NJ, Jeffreys AJ. A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16. Genomics 1990;7:222-34. [PMID: 1971807 DOI: 10.1016/0888-7543(90)90544-5] [Cited by in Crossref: 24] [Cited by in F6Publishing: 22] [Article Influence: 0.8] [Reference Citation Analysis]
684 Jeffreys AJ, Wilson V, Neumann R, Keyte J. Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells. Nucleic Acids Res 1988;16:10953-71. [PMID: 3205737 DOI: 10.1093/nar/16.23.10953] [Cited by in Crossref: 319] [Cited by in F6Publishing: 256] [Article Influence: 10.0] [Reference Citation Analysis]
685 Ali S, Wallace R. Enzymatic synthesis of DNA probes complementary to a human variable number tandem repeat locus. Analytical Biochemistry 1989;179:280-3. [DOI: 10.1016/0003-2697(89)90128-0] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.2] [Reference Citation Analysis]
686 John MV, Ali S. Synthetic DNA-Based Genetic Markers Reveal Intra- and Inter-Species DNA Sequence Variability in the Bubalus bubalis and Related Genomes. DNA and Cell Biology 1997;16:369-78. [DOI: 10.1089/dna.1997.16.369] [Cited by in Crossref: 18] [Cited by in F6Publishing: 11] [Article Influence: 0.8] [Reference Citation Analysis]
687 Urbanová M, Kosuth J, Cellárová E. Genetic and biochemical analysis of Hypericum perforatum L. plants regenerated after cryopreservation. Plant Cell Rep 2006;25:140-7. [PMID: 16456647 DOI: 10.1007/s00299-005-0050-0] [Cited by in Crossref: 26] [Cited by in F6Publishing: 13] [Article Influence: 1.7] [Reference Citation Analysis]
688 Isomura M, Tanigami A, Saito H, Harada Y, Katagiri T, Inazawa J, Nakamura Y, Ledbetter DH. Detailed analysis of loss of heterozygosity on chromosome band 17p13 in breast carcinoma on the basis of a high-resolution physical map with 29 markers. Genes Chromosom Cancer 1994;9:173-9. [DOI: 10.1002/gcc.2870090305] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 0.7] [Reference Citation Analysis]
689 Armour JA, Patel I, Thein SL, Fey MF, Jeffreys AJ. Analysis of somatic mutations at human minisatellite loci in tumors and cell lines. Genomics 1989;4:328-34. [DOI: 10.1016/0888-7543(89)90338-8] [Cited by in Crossref: 71] [Cited by in F6Publishing: 66] [Article Influence: 2.2] [Reference Citation Analysis]
690 Keating M. Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease. Circulation 1992;85:1973-86. [DOI: 10.1161/01.cir.85.6.1973] [Cited by in Crossref: 21] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
691 Nickerson DA, Whitehurst C, Boysen C, Charmley P, Kaiser R, Hood L. Identification of clusters of biallelic polymorphic sequence-tagged sites (pSTSs) that generate highly informative and automatable markers for genetic linkage mapping. Genomics 1992;12:377-87. [PMID: 1531472 DOI: 10.1016/0888-7543(92)90388-9] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 1.0] [Reference Citation Analysis]
692 Holliday JA, Hallerman EM, Haak DC. Genotyping and Sequencing Technologies in Population Genetics and Genomics. In: Rajora OP, editor. Population Genomics. Cham: Springer International Publishing; 2019. pp. 83-125. [DOI: 10.1007/13836_2017_5] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]
693 Burmeister M, diSibio G, Cox DR, Myers RM. Identification of polymorphisms by genomic denaturing gradient gel electrophoresis: application to the proximal region of human chromosome 21. Nucleic Acids Res 1991;19:1475-81. [PMID: 1674130 DOI: 10.1093/nar/19.7.1475] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 0.4] [Reference Citation Analysis]
694 Sarkar G, Paynton C, Sommer SS. Segments containing alternating purine and pyrimidine dinucleotides: patterns of polymorphism in humans and prevalence throughout phylogeny. Nucleic Acids Res 1991;19:631-6. [PMID: 2011533 DOI: 10.1093/nar/19.3.631] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 0.6] [Reference Citation Analysis]
695 Bishop AJR, Louis EJ, Borts RH. Minisatellite Variants Generated in Yeast Meiosis Involve DNA Removal During Gene Conversion. Genetics 2000;156:7-20. [DOI: 10.1093/genetics/156.1.7] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 0.6] [Reference Citation Analysis]
696 Washio K, Misawa S, Ueda S. Probe walking: development of novel probes for DNA fingerprinting. Hum Genet 1989;83:223-6. [DOI: 10.1007/bf00285160] [Cited by in Crossref: 9] [Article Influence: 0.3] [Reference Citation Analysis]
697 Epplen JT, Ammer H, Epplen C, Kammerbauer C, Mitreiter R, Roewer L, Schwaiger W, Steimle V, Zischler H, Albert E, Andreas A, Beyermann B, Meyer W, Buitkamp J, Nanda I, Schmid M, Nürnberg P, Pena SDJ, Pöche H, Sprecher W, Schartl M, Weising K, Yassouridis A. Oligonucleotide Fingerprinting Using Simple Repeat Motifs: A Convenient, Ubiquitously Applicable Method to Detect Hypervariability for Multiple Purposes. In: Burke T, Dolf G, Jeffreys AJ, Wolff R, editors. DNA Fingerprinting: Approaches and Applications. Basel: Birkhäuser; 1991. pp. 50-69. [DOI: 10.1007/978-3-0348-7312-3_4] [Cited by in Crossref: 57] [Cited by in F6Publishing: 26] [Article Influence: 1.9] [Reference Citation Analysis]
698 Mukabana WR, Takken W, Knols BG. Analysis of arthropod bloodmeals using molecular genetic markers. Trends Parasitol 2002;18:505-9. [PMID: 12473367 DOI: 10.1016/s1471-4922(02)02364-4] [Cited by in Crossref: 63] [Cited by in F6Publishing: 33] [Article Influence: 3.5] [Reference Citation Analysis]
699 Wallace AM, Sandford AJ. Therapeutic response to asthma medications: genotype predictors. Treat Respir Med 2004;3:161-71. [PMID: 15219175 DOI: 10.2165/00151829-200403030-00004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
700 Kreutz R, Higuchi M, Ganten D. Molecular Genetics of Hypertension. Clinical and Experimental Hypertension Part A: Theory and Practice 2009;14:15-34. [DOI: 10.3109/10641969209036168] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
701 Lothe RA, Hastie N, Heimdal K, Fosså SD, Stenwig AE, Børresen A. Frequent loss of 11p13 and 11p15 loci in male germ cell tumours. Genes Chromosom Cancer 1993;7:96-101. [DOI: 10.1002/gcc.2870070206] [Cited by in Crossref: 31] [Cited by in F6Publishing: 30] [Article Influence: 1.1] [Reference Citation Analysis]
702 Houng HS, Lott L, Gong H, Kuschner RA, Lynch JA, Metzgar D. Adenovirus microsatellite reveals dynamics of transmission during a recent epidemic of human adenovirus serotype 14 infection. J Clin Microbiol 2009;47:2243-8. [PMID: 19403773 DOI: 10.1128/JCM.01659-08] [Cited by in Crossref: 16] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
703 Sen D, Gilbert W. A sodium-potassium switch in the formation of four-stranded G4-DNA. Nature 1990;344:410-4. [DOI: 10.1038/344410a0] [Cited by in Crossref: 553] [Cited by in F6Publishing: 513] [Article Influence: 17.8] [Reference Citation Analysis]
704 Lem J, Chin AC, Thayer MJ, Leach RJ, Fournier RE. Coordinate regulation of two genes encoding gluconeogenic enzymes by the trans-dominant locus Tse-1. Proc Natl Acad Sci U S A 1988;85:7302-6. [PMID: 2902627 DOI: 10.1073/pnas.85.19.7302] [Cited by in Crossref: 28] [Cited by in F6Publishing: 30] [Article Influence: 0.8] [Reference Citation Analysis]
705 Fujimoto M, Fults DW, Thomas GA, Nakamura Y, Heilbrun MP, White R, Story JL, Naylor SL, Kagan-Hallet KS, Sheridan PJ. Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme. Genomics 1989;4:210-4. [PMID: 2544511 DOI: 10.1016/0888-7543(89)90302-9] [Cited by in Crossref: 73] [Cited by in F6Publishing: 62] [Article Influence: 2.3] [Reference Citation Analysis]
706 Bashamboo A, Ali S. Minisatellite associated sequence amplification (MASA) of the hypervariable repeat marker 33.15 reveals a male specific band in humans. Molecular and Cellular Probes 2001;15:89-92. [DOI: 10.1006/mcpr.2001.0350] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
707 Choudhary M, Strassmann JE, Solís CR, Queller DC. Microsatellite variation in a social insect. Biochem Genet 1993;31:87-96. [PMID: 8471026 DOI: 10.1007/BF02399822] [Cited by in Crossref: 32] [Cited by in F6Publishing: 3] [Article Influence: 1.1] [Reference Citation Analysis]
708 Herrington CS, Mcgee JO. Interphase cytogenetics. Neurochem Res 1990;15:467-74. [DOI: 10.1007/bf00969934] [Cited by in Crossref: 11] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
709 Nakamura Y, Hoff M, Ballard L, O'Connell P, Leppert M, Lathrop GM, Lalouel JM, White R. Isolation and mapping of a polymorphic DNA sequence (cMHZ47) on chromosome 13 [D13S52]. Nucleic Acids Res 1988;16:3119. [PMID: 2897112 DOI: 10.1093/nar/16.7.3119] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.0] [Reference Citation Analysis]
710 Kaiser R, Tremblay PB, Roots I, Brockmöller J. Validity of PCR with emphasis on variable number of tandem repeat analysis. Clin Biochem 2002;35:49-56. [PMID: 11937078 DOI: 10.1016/s0009-9120(02)00273-4] [Cited by in Crossref: 29] [Cited by in F6Publishing: 8] [Article Influence: 1.5] [Reference Citation Analysis]
711 Rapola J, Järvelä I, Peltonen L. The neuronal ceroid lipofuscinoses: unfolding the genetic defect. Pediatr Pathol 1991;11:799-806. [PMID: 1663617 DOI: 10.3109/15513819109065477] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.1] [Reference Citation Analysis]
712 Deininger PL, Batzer MA. Evolution of Retroposons. In: Hecht MK, Macintyre RJ, Clegg MT, editors. Evolutionary Biology. Boston: Springer US; 1993. pp. 157-96. [DOI: 10.1007/978-1-4615-2878-4_5] [Cited by in Crossref: 72] [Cited by in F6Publishing: 44] [Article Influence: 2.6] [Reference Citation Analysis]
713 Genovese LM, Geraci F, Corrado L, Mangano E, D'Aurizio R, Bordoni R, Severgnini M, Manzini G, De Bellis G, D'Alfonso S, Pellegrini M. A Census of Tandemly Repeated Polymorphic Loci in Genic Regions Through the Comparative Integration of Human Genome Assemblies. Front Genet 2018;9:155. [PMID: 29770143 DOI: 10.3389/fgene.2018.00155] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
714 Liu Y-, Ikeda TM, Tsunewaki K. Moderately repeated, dispersed, and highly variable (MRDHV) genomic sequences of common wheat usable for cultivar identification. Theoret Appl Genetics 1992;84-84:535-43. [DOI: 10.1007/bf00224149] [Cited by in Crossref: 15] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
715