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Cited by 402

The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.

Large multiallelic copy number variations in humans

Handsaker, Robert E, Van Doren, Vanessa, Berman, Jennifer R, Genovese, Giulio, Kashin, Seva, Boettger, Linda M, McCarroll, Steven A·2015·Nature Genetics
DOI 10.1038/ng.3200PMC PMC4405206
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  3. de Cid, R. et al. Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. Nat. Genet. 41, 211–215 (2009). · DOI
  4. McCarroll, S.A. et al. Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease. Nat. Genet. 41, 1341–1344 (2009). · DOI
  5. Willer, C.J. et al. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat. Genet. 41, 25–34 (2009). · DOI · Paper page
  6. McCarroll, S.A. et al. Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease. Nat. Genet. 40, 1107–1112 (2008). · DOI · Paper page
  7. Handsaker, R.E., Korn, J.M., Nemesh, J. & McCarroll, S.A. Discovery and genotyping of genome structural polymorphism by sequencing on a population scale. Nat. Genet. 43, 269–276 (2011). · DOI
  8. Hollox, E.J., Armour, J.A. & Barber, J.C. Extensive normal copy number variation of a β-defensin antimicrobial-gene cluster. Am. J. Hum. Genet. 73, 591–600 (2003). · DOI
  9. Perry, G.H. et al. Diet and the evolution of human amylase gene copy number variation. Nat. Genet. 39, 1256–1260 (2007). · DOI
  10. Perry, G.H. et al. The fine-scale and complex architecture of human copy-number variation. Am. J. Hum. Genet. 82, 685–695 (2008). · DOI
  11. Gu, W., Zhang, F. & Lupski, J.R. Mechanisms for human genomic rearrangements. Pathogenetics 1, 4 (2008). · DOI
  12. Sudmant, P.H. et al. Diversity of human copy number variation and multicopy genes. Science 330, 641–646 (2010). · DOI · Paper page
  13. Yoon, S., Xuan, Z., Makarov, V., Ye, K. & Sebat, J. Sensitive and accurate detection of copy number variants using read depth of coverage. Genome Res. 19, 1586–1592 (2009). · DOI
  14. Abyzov, A., Urban, A.E., Snyder, M. & Gerstein, M. CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. Genome Res. 21, 974–984 (2011). · DOI · Paper page
  15. Bellos, E., Johnson, M.R. & Coin, L.J. cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data. Genome Biol. 13, R120 (2012). · DOI
  16. Koren, A. et al. Genetic variation in human DNA replication timing. Cell 159, 1015–1026 (2014). · DOI
  17. Wang, Y., Lu, J., Yu, J., Gibbs, R.A. & Yu, F. An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data. Genome Res. 23, 833–842 (2013). · DOI
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  21. Boettger, L.M., Handsaker, R.E., Zody, M.C. & McCarroll, S.A. Structural haplotypes and recent evolution of the human 17q21.31 region. Nat. Genet. 44, 881–885 (2012). · DOI
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  34. Zanda, M. et al. A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes. PLoS Genet. 10, e1004367 (2014). · DOI
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Cited by

Metadata

Authors
Handsaker, R. E., Van Doren, V., Berman, J. R., Genovese, G., Kashin, S., Boettger, L. M., & McCarroll, S. A.
Venue
Nature Genetics
Publisher
Springer Science and Business Media LLC
Published
2015-01-26
Volume
47
Issue
3
Pages
296-303
ISSN
  • 1061-4036
  • 1546-1718
DOI
10.1038/ng.3200
PMC
PMC4405206
Cited by
402
References
17
Language
en
Licence
www.springer.com/tdm (tdm)

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