Widening the spectrum of human genetic variation - PubMed

Comment

Widening the spectrum of human genetic variation

Evan E Eichler. Nat Genet. 2006 Jan.

Comment on

• A high-resolution survey of deletion polymorphism in the human genome.

  Conrad DF, Andrews TD, Carter NP, Hurles ME, Pritchard JK. Conrad DF, et al. Nat Genet. 2006 Jan;38(1):75-81. doi: 10.1038/ng1697. Epub 2005 Dec 4. Nat Genet. 2006. PMID: 16327808

• Common deletions and SNPs are in linkage disequilibrium in the human genome.

  Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA. Hinds DA, et al. Nat Genet. 2006 Jan;38(1):82-5. doi: 10.1038/ng1695. Epub 2005 Dec 4. Nat Genet. 2006. PMID: 16327809

• Common deletion polymorphisms in the human genome.

  McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, Dallaire S, Gabriel SB, Lee C, Daly MJ, Altshuler DM; International HapMap Consortium. McCarroll SA, et al. Nat Genet. 2006 Jan;38(1):86-92. doi: 10.1038/ng1696. Nat Genet. 2006. PMID: 16468122

Similar articles

• [Methods for large-scale analyses of human genome diversity].

  Kukita Y, Hayashi K. Kukita Y, et al. Tanpakushitsu Kakusan Koso. 2001 Dec;46(16 Suppl):2283-8. Tanpakushitsu Kakusan Koso. 2001. PMID: 11802380 Review. Japanese. No abstract available.

• Structural variation in the human genome.

  Feuk L, Carson AR, Scherer SW. Feuk L, et al. Nat Rev Genet. 2006 Feb;7(2):85-97. doi: 10.1038/nrg1767. Nat Rev Genet. 2006. PMID: 16418744 Review.

• [Structural variation in the human genome contributes to variation of traits].

  Barøy T, Misceo D, Frengen E. Barøy T, et al. Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1951-5. Tidsskr Nor Laegeforen. 2008. PMID: 18787571 Review. Norwegian.

• Characterization of frequencies and distribution of single nucleotide insertions/deletions in the human genome.

  Tan EC, Li H. Tan EC, et al. Gene. 2006 Jul 19;376(2):268-80. doi: 10.1016/j.gene.2006.04.009. Epub 2006 May 3. Gene. 2006. PMID: 16781088

• Structural variants deconstruct the genome.

  [No authors listed] [No authors listed] Nat Genet. 2006 Sep;38(9):959. doi: 10.1038/ng0906-959. Nat Genet. 2006. PMID: 16940994

Cited by

• Strategies for the detection of copy number and other structural variants in the human genome.

  Carson AR, Feuk L, Mohammed M, Scherer SW. Carson AR, et al. Hum Genomics. 2006 Jun;2(6):403-14. doi: 10.1186/1479-7364-2-6-403. Hum Genomics. 2006. PMID: 16848978 Free PMC article. Review.

• Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays.

  Auer H, Newsom DL, Nowak NJ, McHugh KM, Singh S, Yu CY, Yang Y, Wenger GD, Gastier-Foster JM, Kornacker K. Auer H, et al. BMC Genomics. 2007 Apr 30;8:111. doi: 10.1186/1471-2164-8-111. BMC Genomics. 2007. PMID: 17470268 Free PMC article.

• The impact of human copy number variation on gene expression.

  Gamazon ER, Stranger BE. Gamazon ER, et al. Brief Funct Genomics. 2015 Sep;14(5):352-7. doi: 10.1093/bfgp/elv017. Epub 2015 Apr 27. Brief Funct Genomics. 2015. PMID: 25922366 Free PMC article. Review.

• Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex.

  Poot M, Eleveld MJ, van 't Slot R, Ploos van Amstel HK, Hochstenbach R. Poot M, et al. Eur J Hum Genet. 2010 Jan;18(1):39-46. doi: 10.1038/ejhg.2009.120. Eur J Hum Genet. 2010. PMID: 19623214 Free PMC article.

• Copy number variation in human health, disease, and evolution.

  Zhang F, Gu W, Hurles ME, Lupski JR. Zhang F, et al. Annu Rev Genomics Hum Genet. 2009;10:451-81. doi: 10.1146/annurev.genom.9.081307.164217. Annu Rev Genomics Hum Genet. 2009. PMID: 19715442 Free PMC article. Review.

Publication types

MeSH terms

LinkOut - more resources

• Full Text Sources

  • Nature Publishing Group

• Other Literature Sources

  • The Lens - Patent Citations Database