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Items: 15

1.

Bias of selection on human copy-number variants.

Nguyen DQ, Webber C, Ponting CP.

PLoS Genet. 2006 Feb;2(2):e20. Epub 2006 Feb 17.

2.

Copy number polymorphism in plant genomes.

Żmieńko A, Samelak A, Kozłowski P, Figlerowicz M.

Theor Appl Genet. 2014 Jan;127(1):1-18. doi: 10.1007/s00122-013-2177-7. Epub 2013 Aug 29. Review.

3.

Mutational and selective effects on copy-number variants in the human genome.

Cooper GM, Nickerson DA, Eichler EE.

Nat Genet. 2007 Jul;39(7 Suppl):S22-9. Review.

PMID:
17597777
4.

Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease.

Colobran R, Pedrosa E, Carretero-Iglesia L, Juan M.

Clin Exp Immunol. 2010 Oct;162(1):41-52. doi: 10.1111/j.1365-2249.2010.04224.x. Epub 2010 Aug 19. Review.

5.

Copy-number variation in control population cohorts.

Pinto D, Marshall C, Feuk L, Scherer SW.

Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R168-73. Review. Erratum in: Hum Mol Genet. 2008 Feb 1;17(3):166-7.

PMID:
17911159
6.

Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders.

Iyer J, Girirajan S.

Brief Funct Genomics. 2015 Sep;14(5):315-28. doi: 10.1093/bfgp/elv018. Epub 2015 May 13. Review.

PMID:
25971441
7.

Gene copy-number polymorphism in nature.

Schrider DR, Hahn MW.

Proc Biol Sci. 2010 Nov 7;277(1698):3213-21. doi: 10.1098/rspb.2010.1180. Epub 2010 Jun 30. Review.

8.

CNVs of noncoding cis-regulatory elements in human disease.

Spielmann M, Klopocki E.

Curr Opin Genet Dev. 2013 Jun;23(3):249-56. doi: 10.1016/j.gde.2013.02.013. Epub 2013 Apr 16. Review.

PMID:
23601627
9.

Copy number variants and selective sweeps in natural populations of the house mouse (Mus musculus domesticus).

Bryk J, Tautz D.

Front Genet. 2014 Jun 3;5:153. doi: 10.3389/fgene.2014.00153. eCollection 2014. Review.

10.

Copy number variants (CNVs) in primate species using array-based comparative genomic hybridization.

Gökçümen O, Lee C.

Methods. 2009 Sep;49(1):18-25. doi: 10.1016/j.ymeth.2009.06.001. Epub 2009 Jun 21. Review.

11.

Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus.

Wu YL, Yang Y, Chung EK, Zhou B, Kitzmiller KJ, Savelli SL, Nagaraja HN, Birmingham DJ, Tsao BP, Rovin BH, Hebert LA, Yu CY.

Cytogenet Genome Res. 2008;123(1-4):131-41. doi: 10.1159/000184700. Epub 2009 Mar 11. Review.

12.

Copy-number variations, noncoding sequences, and human phenotypes.

Klopocki E, Mundlos S.

Annu Rev Genomics Hum Genet. 2011;12:53-72. doi: 10.1146/annurev-genom-082410-101404. Review.

PMID:
21756107
13.

Copy number variants, diseases and gene expression.

Henrichsen CN, Chaignat E, Reymond A.

Hum Mol Genet. 2009 Apr 15;18(R1):R1-8. doi: 10.1093/hmg/ddp011. Review.

PMID:
19297395
14.

Copy-number variation: the end of the human genome?

Dear PH.

Trends Biotechnol. 2009 Aug;27(8):448-54. doi: 10.1016/j.tibtech.2009.05.003. Epub 2009 Jul 1. Review.

PMID:
19576644
15.

Functional enrichment analysis with structural variants: pitfalls and strategies.

Webber C.

Cytogenet Genome Res. 2011;135(3-4):277-85. doi: 10.1159/000331670. Epub 2011 Oct 12. Review.

PMID:
21997137

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