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For: Gu W, Zhang F, Lupski JR. Mechanisms for human genomic rearrangements. Pathogenetics. 2008;1:4. [PMID: 19014668 DOI: 10.1186/1755-8417-1-4] [Cited by in Crossref: 389] [Cited by in F6Publishing: 364] [Article Influence: 27.8] [Reference Citation Analysis]
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2 Blazejewski SM, Bennison SA, Smith TH, Toyo-Oka K. Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3. Front Genet 2018;9:80. [PMID: 29628935 DOI: 10.3389/fgene.2018.00080] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 7.0] [Reference Citation Analysis]
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4 Branzei D. Ubiquitin family modifications and template switching. FEBS Lett 2011;585:2810-7. [PMID: 21539841 DOI: 10.1016/j.febslet.2011.04.053] [Cited by in Crossref: 58] [Cited by in F6Publishing: 55] [Article Influence: 5.3] [Reference Citation Analysis]
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6 Black HA, Khan FF, Tyson J, Al Armour J. Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus. BMC Genomics 2014;15:614. [PMID: 25048054 DOI: 10.1186/1471-2164-15-614] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
7 Zmienko A, Marszalek-Zenczak M, Wojciechowski P, Samelak-Czajka A, Luczak M, Kozlowski P, Karlowski WM, Figlerowicz M. AthCNV: A Map of DNA Copy Number Variations in the Arabidopsis Genome. Plant Cell 2020;32:1797-819. [PMID: 32265262 DOI: 10.1105/tpc.19.00640] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 4.5] [Reference Citation Analysis]
8 Livnat A. Interaction-based evolution: how natural selection and nonrandom mutation work together. Biol Direct 2013;8:24. [PMID: 24139515 DOI: 10.1186/1745-6150-8-24] [Cited by in Crossref: 22] [Cited by in F6Publishing: 14] [Article Influence: 2.4] [Reference Citation Analysis]
9 Negri G, Magini P, Milani D, Colapietro P, Rusconi D, Scarano E, Bonati MT, Priolo M, Crippa M, Mazzanti L, Wischmeijer A, Tamburrino F, Pippucci T, Finelli P, Larizza L, Gervasini C. From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients: New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks. Hum Mutat 2016;37:175-83. [PMID: 26486927 DOI: 10.1002/humu.22922] [Cited by in Crossref: 24] [Cited by in F6Publishing: 26] [Article Influence: 3.4] [Reference Citation Analysis]
10 Huang J, Wu X, Montenegro G, Price J, Wang G, Vance JM, Shy ME, Züchner S. Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease. J Neurol 2010;257:735-41. [PMID: 19949810 DOI: 10.1007/s00415-009-5401-2] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 1.5] [Reference Citation Analysis]
11 Nakamura Y, Ando Y, Takagi Y, Murata M, Kozuka T, Nakata Y, Hasebe R, Takagi A, Matsushita T, Shima M, Kojima T. Distinct X chromosomal rearrangements in four haemophilia B patients with entire F9 deletion. Haemophilia 2016;22:433-9. [PMID: 26686734 DOI: 10.1111/hae.12849] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
12 Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, Macarthur DG, Macdonald JR, Onyiah I, Pang AW, Robson S, Stirrups K, Valsesia A, Walter K, Wei J; Wellcome Trust Case Control Consortium, Tyler-Smith C, Carter NP, Lee C, Scherer SW, Hurles ME. Origins and functional impact of copy number variation in the human genome. Nature. 2010;464:704-712. [PMID: 19812545 DOI: 10.1038/nature08516] [Cited by in Crossref: 1305] [Cited by in F6Publishing: 1215] [Article Influence: 100.4] [Reference Citation Analysis]
13 Gill M. Developmental psychopathology: The role of structural variation in the genome. Dev Psychopathol 2012;24:1319-34. [DOI: 10.1017/s0954579412000739] [Cited by in Crossref: 10] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Fan X, Pinthong K, de Oliveira EHC, Tanomtong A, Chen H, Weise A, Liehr T. First Comprehensive Characterization of Phayre’s Leaf-Monkey (Trachypithecus phayrei) Karyotype. Front Genet 2022;13:841681. [DOI: 10.3389/fgene.2022.841681] [Reference Citation Analysis]
15 Fukushi D, Yamada K, Nomura N, Naiki M, Kimura R, Yamada Y, Kumagai T, Yamaguchi K, Miyake Y, Wakamatsu N. Clinical characterization and identification of duplication breakpoints in a Japanese family with Xq28 duplication syndrome including MECP2. Am J Med Genet A 2014;164A:924-33. [PMID: 24478188 DOI: 10.1002/ajmg.a.36373] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.9] [Reference Citation Analysis]
16 Yang Q, Shen Y, Shao C, Liu Y, Xu H, Zhou Y, Liu Z, Sun K, Tang Q, Xie J. Genetic analysis of tri-allelic patterns at the CODIS STR loci. Mol Genet Genomics 2020;295:1263-8. [DOI: 10.1007/s00438-020-01701-w] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
17 Halliwell JA, Baker D, Judge K, Quail MA, Oliver K, Betteridge E, Skelton J, Andrews PW, Barbaric I. Nanopore Sequencing Indicates That Tandem Amplification of Chromosome 20q11.21 in Human Pluripotent Stem Cells Is Driven by Break-Induced Replication. Stem Cells Dev 2021;30:578-86. [PMID: 33757297 DOI: 10.1089/scd.2021.0013] [Reference Citation Analysis]
18 Genesio R, Ronga V, Castelluccio P, Fioretti G, Mormile A, Leone G, Conti A, Cavaliere ML, Nitsch L. Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event. Mol Cytogenet 2013;6:29. [PMID: 23915422 DOI: 10.1186/1755-8166-6-29] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
19 Fontana P, Genesio R, Casertano A, Cappuccio G, Mormile A, Nitsch L, Iolascon A, Andria G, Melis D. Loeys–Dietz syndrome type 4, caused by chromothripsis, involving the TGFB2 gene. Gene 2014;538:69-73. [DOI: 10.1016/j.gene.2014.01.017] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 1.6] [Reference Citation Analysis]
20 Rahn JJ, Adair GM, Nairn RS. Multiple roles of ERCC1-XPF in mammalian interstrand crosslink repair. Environ Mol Mutagen 2010;51:567-81. [PMID: 20658648 DOI: 10.1002/em.20583] [Cited by in Crossref: 8] [Cited by in F6Publishing: 19] [Article Influence: 0.7] [Reference Citation Analysis]
21 Lysák MA, Schubert I. Mechanisms of Chromosome Rearrangements. In: Greilhuber J, Dolezel J, Wendel JF, editors. Plant Genome Diversity Volume 2. Vienna: Springer; 2013. pp. 137-47. [DOI: 10.1007/978-3-7091-1160-4_9] [Cited by in Crossref: 25] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
22 Ge L, Liu A, Gao K, Du R, Ding J, Mao B, Hua Y, Zhang X, Tan D, Yang H, Fu X, Fan Y, Zhang L, Song S, Wu J, Zhang F, Jiang Y, Wu X, Xiong H. Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. Sci Rep 2018;8:14989. [PMID: 30301903 DOI: 10.1038/s41598-018-33098-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
23 Friedrich K, Lee L, Leistritz DF, Nürnberg G, Saha B, Hisama FM, Eyman DK, Lessel D, Nürnberg P, Li C, Garcia-F-Villalta MJ, Kets CM, Schmidtke J, Cruz VT, Van den Akker PC, Boak J, Peter D, Compoginis G, Cefle K, Ozturk S, López N, Wessel T, Poot M, Ippel PF, Groff-Kellermann B, Hoehn H, Martin GM, Kubisch C, Oshima J. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations. Hum Genet 2010;128:103-11. [PMID: 20443122 DOI: 10.1007/s00439-010-0832-5] [Cited by in Crossref: 62] [Cited by in F6Publishing: 53] [Article Influence: 5.2] [Reference Citation Analysis]
24 Gimelli S, Chrast J, Baban A, Henrichsen CN, Lerone M, Zuffardi O, Gimelli G, Reymond A. A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromes. Am J Med Genet A 2010;152A:1285-94. [PMID: 20425838 DOI: 10.1002/ajmg.a.33365] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
25 Casamassa A, Ferrari D, Gelati M, Carella M, Vescovi AL, Rosati J. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15. Int J Mol Sci 2020;21:E1860. [PMID: 32182809 DOI: 10.3390/ijms21051860] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
26 Lannoy N, Bandelier C, Grisart B, Reginster M, Ronge-collard E, Vikkula M, Hermans C. Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A. Haemophilia 2015;21:516-22. [DOI: 10.1111/hae.12675] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
27 Molina O, Anton E, Vidal F, Blanco J. High rates of de novo 15q11q13 inversions in human spermatozoa. Mol Cytogenet 2012;5:11. [PMID: 22309495 DOI: 10.1186/1755-8166-5-11] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.6] [Reference Citation Analysis]
28 Ferri L, Donati MA, Funghini S, Cavicchi C, Pensato V, Gellera C, Natacci F, Spaccini L, Gasperini S, Vaz FM, Cooper DN, Guerrini R, Morrone A. Intra-individual plasticity of the TAZ gene leading to different heritable mutations in siblings with Barth syndrome. Eur J Hum Genet 2015;23:1708-12. [PMID: 25782672 DOI: 10.1038/ejhg.2015.50] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
29 Barbaro M, Kotajärvi M, Harper P, Floderus Y. Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyria. Clin Genet 2012;81:249-56. [PMID: 21231929 DOI: 10.1111/j.1399-0004.2011.01628.x] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
30 [DOI: 10.1101/087981] [Cited by in Crossref: 10] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
31 Ding X, Zhang Z, Hu R, Wen Y, Huang Y, Shi Q, Feng Y, Wang E, Lei C, He H. A molecular marker of milk composition traits in NCAM2 gene of Chinese Holstein. Anim Biotechnol 2020;:1-6. [PMID: 33314987 DOI: 10.1080/10495398.2020.1772802] [Reference Citation Analysis]
32 Ter Brugge P, Kristel P, van der Burg E, Boon U, de Maaker M, Lips E, Mulder L, de Ruiter J, Moutinho C, Gevensleben H, Marangoni E, Majewski I, Józwiak K, Kloosterman W, van Roosmalen M, Duran K, Hogervorst F, Turner N, Esteller M, Cuppen E, Wesseling J, Jonkers J. Mechanisms of Therapy Resistance in Patient-Derived Xenograft Models of BRCA1-Deficient Breast Cancer. J Natl Cancer Inst 2016;108. [PMID: 27381626 DOI: 10.1093/jnci/djw148] [Cited by in Crossref: 78] [Cited by in F6Publishing: 73] [Article Influence: 13.0] [Reference Citation Analysis]
33 Bickhart DM, Liu GE. The challenges and importance of structural variation detection in livestock. Front Genet 2014;5:37. [PMID: 24600474 DOI: 10.3389/fgene.2014.00037] [Cited by in Crossref: 58] [Cited by in F6Publishing: 47] [Article Influence: 7.3] [Reference Citation Analysis]
34 Clop A, Vidal O, Amills M. Copy number variation in the genomes of domestic animals. Anim Genet 2012;43:503-17. [PMID: 22497594 DOI: 10.1111/j.1365-2052.2012.02317.x] [Cited by in Crossref: 89] [Cited by in F6Publishing: 77] [Article Influence: 8.9] [Reference Citation Analysis]
35 Vergés L, Vidal F, Geán E, Alemany-Schmidt A, Oliver-Bonet M, Blanco J. An exploratory study of predisposing genetic factors for DiGeorge/velocardiofacial syndrome. Sci Rep 2017;7:40031. [PMID: 28059126 DOI: 10.1038/srep40031] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.6] [Reference Citation Analysis]
36 Shearer AE, Kolbe DL, Azaiez H, Sloan CM, Frees KL, Weaver AE, Clark ET, Nishimura CJ, Black-Ziegelbein EA, Smith RJ. Copy number variants are a common cause of non-syndromic hearing loss. Genome Med 2014;6:37. [PMID: 24963352 DOI: 10.1186/gm554] [Cited by in Crossref: 98] [Cited by in F6Publishing: 82] [Article Influence: 12.3] [Reference Citation Analysis]
37 Molina O, Blanco J, Vidal F. Deletions and duplications of the 15q11-q13 region in spermatozoa from Prader-Willi syndrome fathers. Mol Hum Reprod 2010;16:320-8. [PMID: 20083560 DOI: 10.1093/molehr/gaq005] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 0.8] [Reference Citation Analysis]
38 Brand H, Collins RL, Hanscom C, Rosenfeld JA, Pillalamarri V, Stone MR, Kelley F, Mason T, Margolin L, Eggert S, Mitchell E, Hodge JC, Gusella JF, Sanders SJ, Talkowski ME. Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation. Am J Hum Genet 2015;97:170-6. [PMID: 26094575 DOI: 10.1016/j.ajhg.2015.05.012] [Cited by in Crossref: 37] [Cited by in F6Publishing: 31] [Article Influence: 5.3] [Reference Citation Analysis]
39 Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C, Williams C, Stalker H, Hamid R, Hannig V, Abdel-Hamid H, Bader P, McCracken E, Niyazov D, Leppig K, Thiese H, Hummel M, Alexander N, Gorski J, Kussmann J, Shashi V, Johnson K, Rehder C, Ballif BC, Shaffer LG, Eichler EE. A copy number variation morbidity map of developmental delay. Nat Genet 2011;43:838-46. [PMID: 21841781 DOI: 10.1038/ng.909] [Cited by in Crossref: 861] [Cited by in F6Publishing: 780] [Article Influence: 78.3] [Reference Citation Analysis]
40 Fukami M, Shozu M, Ogata T. Molecular bases and phenotypic determinants of aromatase excess syndrome. Int J Endocrinol 2012;2012:584807. [PMID: 22319526 DOI: 10.1155/2012/584807] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
41 Carvalho CM, Zhang F, Lupski JR. Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution. Proc Natl Acad Sci U S A 2010;107 Suppl 1:1765-71. [PMID: 20080665 DOI: 10.1073/pnas.0906222107] [Cited by in Crossref: 45] [Cited by in F6Publishing: 42] [Article Influence: 3.8] [Reference Citation Analysis]
42 Toksoy G, Durmus H, Aghayev A, Bagirova G, Sevinc Rustemoglu B, Basaran S, Avci S, Karaman B, Parman Y, Altunoglu U, Yapici Z, Tekturk P, Deymeer F, Topaloglu H, Kayserili H, Oflazer-serdaroglu P, Uyguner Z. Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling. Neuromuscular Disorders 2019;29:601-13. [DOI: 10.1016/j.nmd.2019.03.012] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
43 Chen C, Ma H, Zhang F, Chen L, Xing X, Wang S, Zhang X, Luo Y. Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients. PLoS One 2014;9:e108038. [PMID: 25244321 DOI: 10.1371/journal.pone.0108038] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 2.3] [Reference Citation Analysis]
44 Moysés-Oliveira M, Di-Battista A, Zamariolli M, Meloni VA, Bragagnolo S, Christofolini DM, Steiner CE, Kosyakova N, Liehr T, Reymond A, Melaragno MI. Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes. Eur J Hum Genet 2019;27:760-71. [PMID: 30700833 DOI: 10.1038/s41431-019-0341-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
45 Sundralingam T, Tennekoon KH, de Silva S, De Silva S, Hewage S, Ranasinghe R. Novel gross deletion at the GHRHR gene locus possibly mediated by Alu specific microhomology identified in a Sri Lankan patient with isolated growth hormone deficiency. Growth Horm IGF Res 2018;42-43:94-101. [PMID: 30390533 DOI: 10.1016/j.ghir.2018.10.005] [Reference Citation Analysis]
46 Freudenberg J, Freudenberg-Hua Y. Testing the genomic enrichment of a large copy number variation within schizophrenia linkage regions. Psychiatr Genet 2012;22:294-7. [PMID: 22914616 DOI: 10.1097/YPG.0b013e3283586231] [Reference Citation Analysis]
47 Nguyen KV. Potential epigenomic co-management in rare diseases and epigenetic therapy. Nucleosides Nucleotides Nucleic Acids 2019;38:752-80. [PMID: 31079569 DOI: 10.1080/15257770.2019.1594893] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
48 Flynn EK, Kamat A, Lach FP, Donovan FX, Kimble DC, Narisu N, Sanborn E, Boulad F, Davies SM, Gillio AP 3rd, Harris RE, MacMillan ML, Wagner JE, Smogorzewska A, Auerbach AD, Ostrander EA, Chandrasekharappa SC. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes. Hum Mutat 2014;35:1342-53. [PMID: 25168418 DOI: 10.1002/humu.22680] [Cited by in Crossref: 6] [Cited by in F6Publishing: 21] [Article Influence: 0.9] [Reference Citation Analysis]
49 Song X, Beck CR, Du R, Campbell IM, Coban-Akdemir Z, Gu S, Breman AM, Stankiewicz P, Ira G, Shaw CA, Lupski JR. Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements. Genome Res 2018;28:1228-42. [PMID: 29907612 DOI: 10.1101/gr.229401.117] [Cited by in Crossref: 37] [Cited by in F6Publishing: 35] [Article Influence: 9.3] [Reference Citation Analysis]
50 Malhotra D, Sebat J. CNVs: harbingers of a rare variant revolution in psychiatric genetics. Cell. 2012;148:1223-1241. [PMID: 22424231 DOI: 10.1016/j.cell.2012.02.039] [Cited by in Crossref: 580] [Cited by in F6Publishing: 485] [Article Influence: 58.0] [Reference Citation Analysis]
51 Kim S, Mun S, Kim T, Lee KH, Kang K, Cho JY, Han K. Transposable element-mediated structural variation analysis in dog breeds using whole-genome sequencing. Mamm Genome 2019;30:289-300. [PMID: 31414176 DOI: 10.1007/s00335-019-09812-5] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
52 Koscinski I, Elinati E, Fossard C, Redin C, Muller J, Velez de la Calle J, Schmitt F, Ben Khelifa M, Ray PF, Kilani Z, Barratt CL, Viville S. DPY19L2 deletion as a major cause of globozoospermia. Am J Hum Genet 2011;88:344-50. [PMID: 21397063 DOI: 10.1016/j.ajhg.2011.01.018] [Cited by in Crossref: 114] [Cited by in F6Publishing: 111] [Article Influence: 10.4] [Reference Citation Analysis]
53 Startek M, Szafranski P, Gambin T, Campbell IM, Hixson P, Shaw CA, Stankiewicz P, Gambin A. Genome-wide analyses of LINE-LINE-mediated nonallelic homologous recombination. Nucleic Acids Res 2015;43:2188-98. [PMID: 25613453 DOI: 10.1093/nar/gku1394] [Cited by in Crossref: 51] [Cited by in F6Publishing: 47] [Article Influence: 7.3] [Reference Citation Analysis]
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55 Yamada M, Arai T, Oishi T, Hatano N, Kobayashi I, Kubota M, Suzuki N, Yoda M, Kawamura N, Ariga T. Determination of the deletion breakpoints in two patients with contiguous gene syndrome encompassing CYBB gene. European Journal of Medical Genetics 2010;53:383-8. [DOI: 10.1016/j.ejmg.2010.08.003] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
56 Kaiser-rogers K, Rao KW. Structural Chromosome Rearrangements. In: Gersen SL, Keagle MB, editors. The Principles of Clinical Cytogenetics. New York: Springer; 2013. pp. 139-74. [DOI: 10.1007/978-1-4419-1688-4_9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
57 Hsiao MC, Piotrowski A, Callens T, Fu C, Wimmer K, Claes KB, Messiaen L. Decoding NF1 Intragenic Copy-Number Variations. Am J Hum Genet 2015;97:238-49. [PMID: 26189818 DOI: 10.1016/j.ajhg.2015.06.002] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 2.3] [Reference Citation Analysis]
58 Wang ZC, Birkbak NJ, Culhane AC, Drapkin R, Fatima A, Tian R, Schwede M, Alsop K, Daniels KE, Piao H, Liu J, Etemadmoghadam D, Miron A, Salvesen HB, Mitchell G, DeFazio A, Quackenbush J, Berkowitz RS, Iglehart JD, Bowtell DD, Matulonis UA; Australian Ovarian Cancer Study Group. Profiles of genomic instability in high-grade serous ovarian cancer predict treatment outcome. Clin Cancer Res 2012;18:5806-15. [PMID: 22912389 DOI: 10.1158/1078-0432.CCR-12-0857] [Cited by in Crossref: 108] [Cited by in F6Publishing: 64] [Article Influence: 10.8] [Reference Citation Analysis]
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