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Items: 1 to 20 of 62

1.

Frequency of new copy number variation in humans.

van Ommen GJ.

Nat Genet. 2005 Apr;37(4):333-4. No abstract available.

PMID:
15800641
2.

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
3.

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.

de Bustos C, Díaz de Ståhl T, Piotrowski A, Mantripragada KK, Buckley PG, Darai E, Hansson CM, Grigelionis G, Menzel U, Dumanski JP.

Genomics. 2006 Aug;88(2):152-62. Epub 2006 May 18.

4.

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.

Locke DP, Sharp AJ, McCarroll SA, McGrath SD, Newman TL, Cheng Z, Schwartz S, Albertson DG, Pinkel D, Altshuler DM, Eichler EE.

Am J Hum Genet. 2006 Aug;79(2):275-90. Epub 2006 Jun 15.

5.

Relative impact of nucleotide and copy number variation on gene expression phenotypes.

Stranger BE, Forrest MS, Dunning M, Ingle CE, Beazley C, Thorne N, Redon R, Bird CP, de Grassi A, Lee C, Tyler-Smith C, Carter N, Scherer SW, Tavaré S, Deloukas P, Hurles ME, Dermitzakis ET.

Science. 2007 Feb 9;315(5813):848-53.

6.

Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution.

Jiang Z, Tang H, Ventura M, Cardone MF, Marques-Bonet T, She X, Pevzner PA, Eichler EE.

Nat Genet. 2007 Nov;39(11):1361-8. Epub 2007 Oct 7.

PMID:
17922013
7.

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.

Lee AS, Gutiérrez-Arcelus M, Perry GH, Vallender EJ, Johnson WE, Miller GM, Korbel JO, Lee C.

Hum Mol Genet. 2008 Apr 15;17(8):1127-36. doi: 10.1093/hmg/ddn002. Epub 2008 Jan 7.

8.

[Copy-number variation: a new pattern of structural diversity in genome].

Wu ZJ, Jin W.

Yi Chuan. 2009 Apr;31(4):339-47. Review. Chinese.

PMID:
19586885
9.

Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1.

Hollox EJ, Barber JC, Brookes AJ, Armour JA.

Genome Res. 2008 Nov;18(11):1686-97. doi: 10.1101/gr.080945.108. Review.

10.

Human genome: patchwork people.

Check E.

Nature. 2005 Oct 20;437(7062):1084-6. No abstract available.

PMID:
16237414
11.

Population structure in copy number variation and SNPs in the CCL4L chemokine gene.

Colobran R, Comas D, Faner R, Pedrosa E, Anglada R, Pujol-Borrell R, Bertranpetit J, Juan M.

Genes Immun. 2008 Jun;9(4):279-88. doi: 10.1038/gene.2008.15. Epub 2008 Mar 27.

PMID:
18368065
12.

Germ-line DNA copy number variation frequencies in a large North American population.

Zogopoulos G, Ha KC, Naqib F, Moore S, Kim H, Montpetit A, Robidoux F, Laflamme P, Cotterchio M, Greenwood C, Scherer SW, Zanke B, Hudson TJ, Bader GD, Gallinger S.

Hum Genet. 2007 Nov;122(3-4):345-53. Epub 2007 Jul 19.

PMID:
17638019
13.

Detecting copy number variation in the human genome using comparative genomic hybridization.

Tchinda J, Lee C.

Biotechniques. 2006 Oct;41(4):385, 387, 389 passim.

14.

What a difference copy number variation makes.

Kehrer-Sawatzki H.

Bioessays. 2007 Apr;29(4):311-3.

PMID:
17373652
15.

Copy-number variations and human disease.

Hegele RA.

Am J Hum Genet. 2007 Aug;81(2):414-5; author reply 415. No abstract available.

16.

Genome structural variation and sporadic disease traits.

Lupski JR.

Nat Genet. 2006 Sep;38(9):974-6. No abstract available.

PMID:
16941003
17.

Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome.

Goidts V, Cooper DN, Armengol L, Schempp W, Conroy J, Estivill X, Nowak N, Hameister H, Kehrer-Sawatzki H.

Hum Genet. 2006 Sep;120(2):270-84. Epub 2006 Jul 13.

PMID:
16838144
18.

A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.

Lin CH, Lin YC, Wu JY, Pan WH, Chen YT, Fann CS.

Genomics. 2009 Oct;94(4):241-6. doi: 10.1016/j.ygeno.2009.06.004. Epub 2009 Jun 25.

19.

As normal as normal can be?

Carter NP.

Nat Genet. 2004 Sep;36(9):931-2.

PMID:
15340426
20.

Genomic drift and copy number variation of sensory receptor genes in humans.

Nozawa M, Kawahara Y, Nei M.

Proc Natl Acad Sci U S A. 2007 Dec 18;104(51):20421-6. Epub 2007 Dec 5.

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