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For: Dear PH. Copy-number variation: the end of the human genome? Trends Biotechnol. 2009;27:448-454. [PMID: 19576644 DOI: 10.1016/j.tibtech.2009.05.003] [Cited by in Crossref: 36] [Cited by in F6Publishing: 28] [Article Influence: 2.8] [Reference Citation Analysis]
Number Citing Articles
1 Upadhyaya M, Spurlock G, Thomas L, Thomas NST, Richards M, Mautner V, Cooper DN, Guha A, Yan J. Microarray-based copy number analysis of neurofibromatosis type-1 (NF1)-associated malignant peripheral nerve sheath tumors reveals a role for Rho-GTPase pathway genes in NF1 tumorigenesis. Hum Mutat 2012;33:763-76. [DOI: 10.1002/humu.22044] [Cited by in Crossref: 41] [Cited by in F6Publishing: 32] [Article Influence: 4.1] [Reference Citation Analysis]
2 Shao Y, Zhang J, Zhang R, Wan J, Zhang W, Yu B. Examination of Smad2 and Smad4 copy-number variations in skin cancers. Clin Transl Oncol 2012;14:138-42. [DOI: 10.1007/s12094-012-0773-7] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.7] [Reference Citation Analysis]
3 Fang Z, Xiong Y, Li J, Liu L, Li M, Zhang C, Zhang W, Wan J. Copy-number increase of AURKA in gastric cancers in a Chinese population: a correlation with tumor progression. Med Oncol 2011;28:1017-22. [PMID: 20585902 DOI: 10.1007/s12032-010-9602-4] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
4 Xiong Y, Fang Z, Zhang C, Qi G, Liu W, Zhang W, Wan J. Copy number increase of HER-2 in colorectal cancers. Oncol Lett 2011;2:331-5. [PMID: 22866086 DOI: 10.3892/ol.2010.225] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
5 Sgaramella V. Variability of our somatic (epi)genomes. Science 2010;329:32-3. [PMID: 20595596 DOI: 10.1126/science.329.5987.32-c] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
6 Yoo J, Ha IC, Chang GT, Jung KS, Park K, Kim Y. CNVAS: Copy Number Variation Analysis System — The analysis tool for genomic alteration with a powerful visualization module. BioChip J 2011;5:265-70. [DOI: 10.1007/s13206-011-5311-0] [Cited by in Crossref: 4] [Article Influence: 0.4] [Reference Citation Analysis]
7 Li Z, Fang ZY, Ding Y, Yao WT, Yang Y, Zhu ZQ, Wang W, Zhang QX. Amplifications of NCOA3 gene in colorectal cancers in a Chinese population. World J Gastroenterol 2012; 18(8): 855-860 [PMID: 22371647 DOI: 10.3748/wjg.v18.i8.855] [Cited by in CrossRef: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
8 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]
9 Cho WC. Recent progress in genetic variants associated with cancer and their implications in diagnostics development. Expert Rev Mol Diagn 2010;10:699-703. [PMID: 20843192 DOI: 10.1586/erm.10.64] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 1.3] [Reference Citation Analysis]
10 Sgaramella V, Astolfi PA. Somatic genome variations interact with environment, genome and epigenome in the determination of the phenotype: A paradigm shift in genomics? DNA Repair (Amst) 2010;9:470-3. [PMID: 20153268 DOI: 10.1016/j.dnarep.2009.11.011] [Cited by in Crossref: 4] [Cited by in F6Publishing: 8] [Article Influence: 0.3] [Reference Citation Analysis]
11 Felekkis K, Voskarides K, Dweep H, Sticht C, Gretz N, Deltas C. Increased Number of MicroRNA Target Sites in Genes Encoded in CNV Regions. Evidence for an Evolutionary Genomic Interaction. Molecular Biology and Evolution 2011;28:2421-4. [DOI: 10.1093/molbev/msr078] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 2.2] [Reference Citation Analysis]
12 Chu F, Feng Q, Qian Y, Zhang C, Fang Z, Shen G. ERBB2 gene amplification in oral squamous cell malignancies: a correlation with tumor progression and gene expression. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2011;112:90-5. [PMID: 21531597 DOI: 10.1016/j.tripleo.2011.01.026] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
13 Fang Z, Xiong Y, Zhang C, Li J, Liu L, Li M, Zhang W, Wan J. Coexistence of copy number increases of ZNF217 and CYP24A1 in colorectal cancers in a Chinese population. Oncol Lett 2010;1:925-30. [PMID: 22966406 DOI: 10.3892/ol_00000163] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
14 Yang H, Zhang C, Zhao X, Wu Q, Fu X, Yu B, Shao Y, Guan M, Zhang W, Wan J, Huang X. Analysis of copy number variations of BS69 in multiple types of hematological malignancies. Ann Hematol 2010;89:959-64. [DOI: 10.1007/s00277-010-0966-5] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.6] [Reference Citation Analysis]
15 Shumay E, Fowler JS, Volkow ND. Genomic features of the human dopamine transporter gene and its potential epigenetic States: implications for phenotypic diversity. PLoS One 2010;5:e11067. [PMID: 20548783 DOI: 10.1371/journal.pone.0011067] [Cited by in Crossref: 53] [Cited by in F6Publishing: 47] [Article Influence: 4.4] [Reference Citation Analysis]
16 Astolfi PA, Salamini F, Sgaramella V. Are we Genomic Mosaics? Variations of the Genome of Somatic Cells can Contribute to Diversify our Phenotypes. Curr Genomics 2010;11:379-86. [PMID: 21358981 DOI: 10.2174/138920210793175949] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 1.2] [Reference Citation Analysis]
17 Zhang J, Gao Y, Zhao X, Guan M, Zhang W, Wan J, Yu B. Investigation of copy-number variations of C8orf4 in hematological malignancies. Med Oncol 2011;28 Suppl 1:S647-52. [PMID: 20878554 DOI: 10.1007/s12032-010-9698-6] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.7] [Reference Citation Analysis]
18 Haitjema A, Mol BM, Kooi IE, Massink MP, Jørgensen JA, Rockx DA, Rooimans MA, de Winter JP, Meijers-Heijboer H, Joenje H, Dorsman JC. Coregulation of FANCA and BRCA1 in human cells. Springerplus 2014;3:381. [PMID: 25161863 DOI: 10.1186/2193-1801-3-381] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
19 Wan J, Gao Y, Zhao X, Wu Q, Fu X, Shao Y, Yang H, Guan M, Yu B, Zhang W. The association between the copy-number variations of ZMAT4 and hematological malignancy. Hematology 2011;16:20-3. [PMID: 21269563 DOI: 10.1179/102453311X12902908411751] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
20 Henry IM, Dilkes BP, Miller ES, Burkart-Waco D, Comai L. Phenotypic consequences of aneuploidy in Arabidopsis thaliana. Genetics 2010;186:1231-45. [PMID: 20876566 DOI: 10.1534/genetics.110.121079] [Cited by in Crossref: 64] [Cited by in F6Publishing: 59] [Article Influence: 5.3] [Reference Citation Analysis]
21 Charney E, English W. Candidate Genes and Political Behavior. Am Polit Sci Rev 2012;106:1-34. [DOI: 10.1017/s0003055411000554] [Cited by in Crossref: 70] [Cited by in F6Publishing: 1] [Article Influence: 7.0] [Reference Citation Analysis]
22 Charney E. Behavior genetics and postgenomics. Behav Brain Sci 2012;35:331-58. [DOI: 10.1017/s0140525x11002226] [Cited by in Crossref: 109] [Cited by in F6Publishing: 23] [Article Influence: 10.9] [Reference Citation Analysis]
23 De S, Babu MM. A time-invariant principle of genome evolution. Proc Natl Acad Sci U S A 2010;107:13004-9. [PMID: 20615949 DOI: 10.1073/pnas.0914454107] [Cited by in Crossref: 37] [Cited by in F6Publishing: 32] [Article Influence: 3.1] [Reference Citation Analysis]
24 Guan M, Liu L, Zhao X, Wu Q, Yu B, Shao Y, Yang H, Fu X, Wan J, Zhang W. Copy number variations of EphA3 are associated with multiple types of hematologic malignancies. Clin Lymphoma Myeloma Leuk 2011;11:50-3. [PMID: 21454190 DOI: 10.3816/CLML.2011.n.006] [Cited by in Crossref: 27] [Cited by in F6Publishing: 14] [Article Influence: 2.5] [Reference Citation Analysis]
25 Cooper DN, Chen JM, Ball EV, Howells K, Mort M, Phillips AD, Chuzhanova N, Krawczak M, Kehrer-Sawatzki H, Stenson PD. Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics. Hum Mutat 2010;31:631-55. [PMID: 20506564 DOI: 10.1002/humu.21260] [Cited by in Crossref: 139] [Cited by in F6Publishing: 108] [Article Influence: 11.6] [Reference Citation Analysis]
26 Ordóñez R, Gallo-Oller G, Martínez-Soto S, Legarra S, Pata-Merci N, Guegan J, Danglot G, Bernheim A, Meléndez B, Rey JA, Castresana JS. Genome-wide microarray expression and genomic alterations by array-CGH analysis in neuroblastoma stem-like cells. PLoS One 2014;9:e113105. [PMID: 25392930 DOI: 10.1371/journal.pone.0113105] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
27 Charney E, English W. Genopolitics and the Science of Genetics. Am Polit Sci Rev 2013;107:382-95. [DOI: 10.1017/s0003055413000099] [Cited by in Crossref: 28] [Article Influence: 3.1] [Reference Citation Analysis]
28 Weiland Y, Lemmer P, Cremer C. Combining FISH with localisation microscopy: Super-resolution imaging of nuclear genome nanostructures. Chromosome Res 2011;19:5-23. [DOI: 10.1007/s10577-010-9171-6] [Cited by in Crossref: 24] [Cited by in F6Publishing: 21] [Article Influence: 2.0] [Reference Citation Analysis]
29 Zhang C, Fang Z, Xiong Y, Li J, Liu L, Li M, Zhang W, Wan J. Copy number increase of aurora kinase A in colorectal cancers: a correlation with tumor progression. Acta Biochimica et Biophysica Sinica 2010;42:834-8. [DOI: 10.1093/abbs/gmq088] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 0.9] [Reference Citation Analysis]
30 Dweep H, Gretz N, Felekkis K. A Schematic Workflow for Collecting Information About the Interaction Between Copy Number Variants and MicroRNAs Using Existing Resources. In: Alvarez ML, Nourbakhsh M, editors. RNA Mapping. New York: Springer; 2014. pp. 307-20. [DOI: 10.1007/978-1-4939-1062-5_26] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]