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Cited by in F6Publishing
For: Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W. Global variation in copy number in the human genome. Nature. 2006;444:444-454. [PMID: 17122850 DOI: 10.1038/nature05329] [Cited by in Crossref: 2799] [Cited by in F6Publishing: 2563] [Article Influence: 174.9] [Reference Citation Analysis]
Number Citing Articles
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3 Zhang R, Mjoseng HK, Hoeve MA, Bauer NG, Pells S, Besseling R, Velugotla S, Tourniaire G, Kishen RE, Tsenkina Y. A thermoresponsive and chemically defined hydrogel for long-term culture of human embryonic stem cells. Nat Commun. 2013;4:1335. [PMID: 23299885 DOI: 10.1038/ncomms2341] [Cited by in Crossref: 92] [Cited by in F6Publishing: 85] [Article Influence: 10.2] [Reference Citation Analysis]
4 Hamet P, Seda O. Current status of genome-wide scanning for hypertension. Curr Opin Cardiol 2007;22:292-7. [PMID: 17556880 DOI: 10.1097/HCO.0b013e328187b502] [Cited by in Crossref: 16] [Cited by in F6Publishing: 4] [Article Influence: 1.1] [Reference Citation Analysis]
5 Kim PM, Korbel JO, Gerstein MB. Positive selection at the protein network periphery: evaluation in terms of structural constraints and cellular context. Proc Natl Acad Sci U S A 2007;104:20274-9. [PMID: 18077332 DOI: 10.1073/pnas.0710183104] [Cited by in Crossref: 99] [Cited by in F6Publishing: 95] [Article Influence: 6.6] [Reference Citation Analysis]
6 Perry GH, Ben-Dor A, Tsalenko A, Sampas N, Rodriguez-Revenga L, Tran CW, Scheffer A, Steinfeld I, Tsang P, Yamada NA, Park HS, Kim JI, Seo JS, Yakhini Z, Laderman S, Bruhn L, Lee C. The fine-scale and complex architecture of human copy-number variation. Am J Hum Genet 2008;82:685-95. [PMID: 18304495 DOI: 10.1016/j.ajhg.2007.12.010] [Cited by in Crossref: 239] [Cited by in F6Publishing: 233] [Article Influence: 17.1] [Reference Citation Analysis]
7 Boudin E, Fijalkowski I, Hendrickx G, Van Hul W. Genetic control of bone mass. Mol Cell Endocrinol 2016;432:3-13. [PMID: 26747728 DOI: 10.1016/j.mce.2015.12.021] [Cited by in Crossref: 37] [Cited by in F6Publishing: 27] [Article Influence: 5.3] [Reference Citation Analysis]
8 Balikova I, Menten B, de Ravel T, Le Caignec C, Thienpont B, Urbina M, Doco-fenzy M, de Rademaeker M, Mortier G, Kooy F, van Den Ende J, Devriendt K, Fryns J, Speleman F, Vermeesch JR. Subtelomeric imbalances in phenotypically normal individuals. Hum Mutat 2007;28:958-67. [DOI: 10.1002/humu.20537] [Cited by in Crossref: 52] [Cited by in F6Publishing: 38] [Article Influence: 3.5] [Reference Citation Analysis]
9 Scott SA, Patel M, Martis S, Lubitz SA, van der Zee S, Yoo C, Edelmann L, Halperin JL, Desnick RJ. Copy number variation and warfarin dosing: evaluation of CYP2C9, VKORC1, CYP4F2, GGCX and CALU. Pharmacogenomics 2012;13:297-307. [PMID: 22188360 DOI: 10.2217/pgs.11.156] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 0.8] [Reference Citation Analysis]
10 Sackton TB, Kulathinal RJ, Bergman CM, Quinlan AR, Dopman EB, Carneiro M, Marth GT, Hartl DL, Clark AG. Population genomic inferences from sparse high-throughput sequencing of two populations of Drosophila melanogaster. Genome Biol Evol 2009;1:449-65. [PMID: 20333214 DOI: 10.1093/gbe/evp048] [Cited by in Crossref: 47] [Cited by in F6Publishing: 42] [Article Influence: 3.6] [Reference Citation Analysis]
11 Zhu C, Li M, Qin S, Zhao F, Fang S. Detection of copy number variation and selection signatures on the X chromosome in Chinese indigenous sheep with different types of tail. Asian-Australas J Anim Sci 2020;33:1378-86. [PMID: 31480185 DOI: 10.5713/ajas.18.0661] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
12 Derks EM, Ayub M, Chambert K, Del Favero J, Johnstone M, MacGregor S, Maclean A, McKechanie AG, McRae AF, Moran JL, Pickard BS, Purcell S, Sklar P, StClair DM, Wray NR, Visscher PM, Blackwood DH. A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability. Am J Med Genet B Neuropsychiatr Genet 2013;162B:847-54. [PMID: 24115684 DOI: 10.1002/ajmg.b.32189] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 1.3] [Reference Citation Analysis]
13 Altmäe S, Esteban FJ, Stavreus-Evers A, Simón C, Giudice L, Lessey BA, Horcajadas JA, Macklon NS, D'Hooghe T, Campoy C, Fauser BC, Salamonsen LA, Salumets A. Guidelines for the design, analysis and interpretation of 'omics' data: focus on human endometrium. Hum Reprod Update 2014;20:12-28. [PMID: 24082038 DOI: 10.1093/humupd/dmt048] [Cited by in Crossref: 85] [Cited by in F6Publishing: 74] [Article Influence: 9.4] [Reference Citation Analysis]
14 Altshuler D, Daly MJ, Lander ES. Genetic mapping in human disease. Science. 2008;322:881-888. [PMID: 18988837 DOI: 10.1126/science.1156409] [Cited by in Crossref: 958] [Cited by in F6Publishing: 789] [Article Influence: 68.4] [Reference Citation Analysis]
15 Huang Q, Guo H, Wang S, Ma Y, Chen H, Li H, Li J, Li X, Yang F, Qiu M, Zhao S, Wang J. A novel circular RNA, circXPO1, promotes lung adenocarcinoma progression by interacting with IGF2BP1. Cell Death Dis 2020;11:1031. [PMID: 33268793 DOI: 10.1038/s41419-020-03237-8] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
16 Daemen A, Gevaert O, Ojeda F, Debucquoy A, Suykens JA, Sempoux C, Machiels JP, Haustermans K, De Moor B. A kernel-based integration of genome-wide data for clinical decision support. Genome Med 2009;1:39. [PMID: 19356222 DOI: 10.1186/gm39] [Cited by in Crossref: 50] [Cited by in F6Publishing: 40] [Article Influence: 3.8] [Reference Citation Analysis]
17 Verdin H, D'haene B, Beysen D, Novikova Y, Menten B, Sante T, Lapunzina P, Nevado J, Carvalho CM, Lupski JR, De Baere E. Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain. PLoS Genet 2013;9:e1003358. [PMID: 23516377 DOI: 10.1371/journal.pgen.1003358] [Cited by in Crossref: 57] [Cited by in F6Publishing: 53] [Article Influence: 6.3] [Reference Citation Analysis]
18 Schweighofer CD, Coombes KR, Majewski T, Barron LL, Lerner S, Sargent RL, O'Brien S, Ferrajoli A, Wierda WG, Czerniak BA, Medeiros LJ, Keating MJ, Abruzzo LV. Genomic variation by whole-genome SNP mapping arrays predicts time-to-event outcome in patients with chronic lymphocytic leukemia: a comparison of CLL and HapMap genotypes. J Mol Diagn 2013;15:196-209. [PMID: 23273604 DOI: 10.1016/j.jmoldx.2012.09.006] [Cited by in Crossref: 20] [Cited by in F6Publishing: 17] [Article Influence: 2.0] [Reference Citation Analysis]
19 Johansson AM, Säll T. The effect of pedigree structure on detection of deletions and other null alleles. Eur J Hum Genet 2008;16:1225-34. [PMID: 18414511 DOI: 10.1038/ejhg.2008.75] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
20 Olsson M, Olsson B, Jacobson P, Thelle DS, Björkegren J, Walley A, Froguel P, Carlsson LM, Sjöholm K. Expression of the selenoprotein S (SELS) gene in subcutaneous adipose tissue and SELS genotype are associated with metabolic risk factors. Metabolism 2011;60:114-20. [PMID: 20619427 DOI: 10.1016/j.metabol.2010.05.011] [Cited by in Crossref: 42] [Cited by in F6Publishing: 37] [Article Influence: 3.8] [Reference Citation Analysis]
21 Scharpf RB, Ruczinski I, Carvalho B, Doan B, Chakravarti A, Irizarry RA. A multilevel model to address batch effects in copy number estimation using SNP arrays. Biostatistics 2011;12:33-50. [PMID: 20625178 DOI: 10.1093/biostatistics/kxq043] [Cited by in Crossref: 30] [Cited by in F6Publishing: 30] [Article Influence: 2.5] [Reference Citation Analysis]
22 Wang Z, Dong X, Ding G, Li Y. Comparing the retention mechanisms of tandem duplicates and retrogenes in human and mouse genomes. Genet Sel Evol 2010;42:24. [PMID: 20584267 DOI: 10.1186/1297-9686-42-24] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.4] [Reference Citation Analysis]
23 Bentley DR, Balasubramanian S, Swerdlow HP, Smith GP, Milton J, Brown CG, Hall KP, Evers DJ, Barnes CL, Bignell HR, Boutell JM, Bryant J, Carter RJ, Keira Cheetham R, Cox AJ, Ellis DJ, Flatbush MR, Gormley NA, Humphray SJ, Irving LJ, Karbelashvili MS, Kirk SM, Li H, Liu X, Maisinger KS, Murray LJ, Obradovic B, Ost T, Parkinson ML, Pratt MR, Rasolonjatovo IM, Reed MT, Rigatti R, Rodighiero C, Ross MT, Sabot A, Sankar SV, Scally A, Schroth GP, Smith ME, Smith VP, Spiridou A, Torrance PE, Tzonev SS, Vermaas EH, Walter K, Wu X, Zhang L, Alam MD, Anastasi C, Aniebo IC, Bailey DM, Bancarz IR, Banerjee S, Barbour SG, Baybayan PA, Benoit VA, Benson KF, Bevis C, Black PJ, Boodhun A, Brennan JS, Bridgham JA, Brown RC, Brown AA, Buermann DH, Bundu AA, Burrows JC, Carter NP, Castillo N, Chiara E Catenazzi M, Chang S, Neil Cooley R, Crake NR, Dada OO, Diakoumakos KD, Dominguez-Fernandez B, Earnshaw DJ, Egbujor UC, Elmore DW, Etchin SS, Ewan MR, Fedurco M, Fraser LJ, Fuentes Fajardo KV, Scott Furey W, George D, Gietzen KJ, Goddard CP, Golda GS, Granieri PA, Green DE, Gustafson DL, Hansen NF, Harnish K, Haudenschild CD, Heyer NI, Hims MM, Ho JT, Horgan AM, Hoschler K, Hurwitz S, Ivanov DV, Johnson MQ, James T, Huw Jones TA, Kang GD, Kerelska TH, Kersey AD, Khrebtukova I, Kindwall AP, Kingsbury Z, Kokko-Gonzales PI, Kumar A, Laurent MA, Lawley CT, Lee SE, Lee X, Liao AK, Loch JA, Lok M, Luo S, Mammen RM, Martin JW, McCauley PG, McNitt P, Mehta P, Moon KW, Mullens JW, Newington T, Ning Z, Ling Ng B, Novo SM, O'Neill MJ, Osborne MA, Osnowski A, Ostadan O, Paraschos LL, Pickering L, Pike AC, Pike AC, Chris Pinkard D, Pliskin DP, Podhasky J, Quijano VJ, Raczy C, Rae VH, Rawlings SR, Chiva Rodriguez A, Roe PM, Rogers J, Rogert Bacigalupo MC, Romanov N, Romieu A, Roth RK, Rourke NJ, Ruediger ST, Rusman E, Sanches-Kuiper RM, Schenker MR, Seoane JM, Shaw RJ, Shiver MK, Short SW, Sizto NL, Sluis JP, Smith MA, Ernest Sohna Sohna J, Spence EJ, Stevens K, Sutton N, Szajkowski L, Tregidgo CL, Turcatti G, Vandevondele S, Verhovsky Y, Virk SM, Wakelin S, Walcott GC, Wang J, Worsley GJ, Yan J, Yau L, Zuerlein M, Rogers J, Mullikin JC, Hurles ME, McCooke NJ, West JS, Oaks FL, Lundberg PL, Klenerman D, Durbin R, Smith AJ. Accurate whole human genome sequencing using reversible terminator chemistry. Nature 2008;456:53-9. [PMID: 18987734 DOI: 10.1038/nature07517] [Cited by in Crossref: 2303] [Cited by in F6Publishing: 2034] [Article Influence: 164.5] [Reference Citation Analysis]
24 Li K, Jing Y, Yang C, Liu S, Zhao Y, He X, Li F, Han J, Li G. Increased leukemia-associated gene expression in benzene-exposed workers. Sci Rep 2014;4:5369. [PMID: 24993241 DOI: 10.1038/srep05369] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 1.4] [Reference Citation Analysis]
25 Stark AL, Zhang W, Zhou T, O'Donnell PH, Beiswanger CM, Huang RS, Cox NJ, Dolan ME. Population differences in the rate of proliferation of international HapMap cell lines. Am J Hum Genet 2010;87:829-33. [PMID: 21109222 DOI: 10.1016/j.ajhg.2010.10.018] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 1.4] [Reference Citation Analysis]
26 Yang TL, Guo Y, Shen H, Li J, Glessner JT, Qiu C, Deng FY, Tian Q, Yu P, Liu YZ, Liu YJ, Hakonarson H, Grant SF, Deng HW. Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study. J Clin Endocrinol Metab 2013;98:E191-5. [PMID: 23175694 DOI: 10.1210/jc.2012-2751] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 1.9] [Reference Citation Analysis]
27 Fang Z, Xiong Y, Li J, Liu L, Zhang W, Zhang C, Wan J. APC gene deletions in gastric adenocarcinomas in a Chinese population: a correlation with tumour progression. Clin Transl Oncol. 2012;14:60-65. [PMID: 22262720 DOI: 10.1007/s12094-012-0762-x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
28 Nagorski J, Allen GI. Genomic region detection via Spatial Convex Clustering. PLoS One 2018;13:e0203007. [PMID: 30204756 DOI: 10.1371/journal.pone.0203007] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
29 Carrell DT. Paternal genetic and epigenetic influences on IVF outcome. Expert Review of Obstetrics & Gynecology 2014;3:359-67. [DOI: 10.1586/17474108.3.3.359] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
30 Garshasbi M, Hadavi V, Habibi H, Kahrizi K, Kariminejad R, Behjati F, Tzschach A, Najmabadi H, Ropers HH, Kuss AW. A defect in the TUSC3 gene is associated with autosomal recessive mental retardation. Am J Hum Genet 2008;82:1158-64. [PMID: 18452889 DOI: 10.1016/j.ajhg.2008.03.018] [Cited by in Crossref: 98] [Cited by in F6Publishing: 89] [Article Influence: 7.0] [Reference Citation Analysis]
31 Antonacci F, Kidd JM, Marques-Bonet T, Ventura M, Siswara P, Jiang Z, Eichler EE. Characterization of six human disease-associated inversion polymorphisms. Hum Mol Genet 2009;18:2555-66. [PMID: 19383631 DOI: 10.1093/hmg/ddp187] [Cited by in Crossref: 90] [Cited by in F6Publishing: 78] [Article Influence: 6.9] [Reference Citation Analysis]
32 Arlt MF, Wilson TE, Glover TW. Replication stress and mechanisms of CNV formation. Curr Opin Genet Dev 2012;22:204-10. [PMID: 22365495 DOI: 10.1016/j.gde.2012.01.009] [Cited by in Crossref: 68] [Cited by in F6Publishing: 63] [Article Influence: 6.8] [Reference Citation Analysis]
33 Fadista J, Thomsen B, Holm LE, Bendixen C. Copy number variation in the bovine genome. BMC Genomics 2010;11:284. [PMID: 20459598 DOI: 10.1186/1471-2164-11-284] [Cited by in Crossref: 112] [Cited by in F6Publishing: 108] [Article Influence: 9.3] [Reference Citation Analysis]
34 Lantieri F, Malacarne M, Gimelli S, Santamaria G, Coviello D, Ceccherini I. Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant Validation. Int J Mol Sci 2017;18:E609. [PMID: 28287439 DOI: 10.3390/ijms18030609] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
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36 Lee KY, Shin E. Application of array comparative genomic hybridization in Korean children under 6 years old with global developmental delay. Korean J Pediatr 2017;60:282-9. [PMID: 29042871 DOI: 10.3345/kjp.2017.60.9.282] [Reference Citation Analysis]
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38 Purdie KJ, Lambert SR, Teh MT, Chaplin T, Molloy G, Raghavan M, Kelsell DP, Leigh IM, Harwood CA, Proby CM, Young BD. Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis. Genes Chromosomes Cancer 2007;46:661-9. [PMID: 17420988 DOI: 10.1002/gcc.20447] [Cited by in Crossref: 65] [Cited by in F6Publishing: 60] [Article Influence: 4.3] [Reference Citation Analysis]
39 Kim S, Kon M, Kang H. A method for generating new datasets based on copy number for cancer analysis. Biomed Res Int 2015;2015:467514. [PMID: 25949998 DOI: 10.1155/2015/467514] [Cited by in Crossref: 2] [Article Influence: 0.3] [Reference Citation Analysis]
40 Gangestad SW. Evolutionary biology looks at behavior genetics. Personality and Individual Differences 2010;49:289-95. [DOI: 10.1016/j.paid.2010.03.005] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 0.9] [Reference Citation Analysis]
41 Yoshida T, Kobayashi T, Itoda M, Muto T, Miyaguchi K, Mogushi K, Shoji S, Shimokawa K, Iida S, Uetake H, Ishikawa T, Sugihara K, Mizushima H, Tanaka H. Clinical omics analysis of colorectal cancer incorporating copy number aberrations and gene expression data. Cancer Inform 2010;9:147-61. [PMID: 20706620 DOI: 10.4137/cin.s3851] [Cited by in Crossref: 23] [Cited by in F6Publishing: 17] [Article Influence: 1.9] [Reference Citation Analysis]
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44 Xu G, Ma H, Nei M, Kong H. Evolution of F-box genes in plants: different modes of sequence divergence and their relationships with functional diversification. Proc Natl Acad Sci U S A 2009;106:835-40. [PMID: 19126682 DOI: 10.1073/pnas.0812043106] [Cited by in Crossref: 189] [Cited by in F6Publishing: 180] [Article Influence: 14.5] [Reference Citation Analysis]
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51 Li X, Galipeau PC, Sanchez CA, Blount PL, Maley CC, Arnaudo J, Peiffer DA, Pokholok D, Gunderson KL, Reid BJ. Single nucleotide polymorphism-based genome-wide chromosome copy change, loss of heterozygosity, and aneuploidy in Barrett's esophagus neoplastic progression. Cancer Prev Res (Phila) 2008;1:413-23. [PMID: 19138988 DOI: 10.1158/1940-6207.CAPR-08-0121] [Cited by in Crossref: 52] [Cited by in F6Publishing: 31] [Article Influence: 4.0] [Reference Citation Analysis]
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