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Items: 1 to 20 of 154

1.

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
2.

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.

PMID:
17922013
3.

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.

PMID:
16838144
4.

Copy number alterations and copy number variation in cancer: close encounters of the bad kind.

Speleman F, Kumps C, Buysse K, Poppe B, Menten B, De Preter K.

Cytogenet Genome Res. 2008;123(1-4):176-82. doi: 10.1159/000184706. Review.

PMID:
19287153
5.

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history.

Kim PM, Lam HY, Urban AE, Korbel JO, Affourtit J, Grubert F, Chen X, Weissman S, Snyder M, Gerstein MB.

Genome Res. 2008 Dec;18(12):1865-74. doi: 10.1101/gr.081422.108.

6.

Identification of large-scale human-specific copy number differences by inter-species array comparative genomic hybridization.

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

Hum Genet. 2006 Mar;119(1-2):185-98.

PMID:
16395594
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.

8.

Comparative analysis of copy number variation in primate genomes.

Kehrer-Sawatzki H, Cooper DN.

Cytogenet Genome Res. 2008;123(1-4):288-96. doi: 10.1159/000184720.

PMID:
19287167
9.

Segmental copy-number variation observed in Japanese by array-CGH.

Takahashi N, Tsuyama N, Sasaki K, Kodaira M, Satoh Y, Kodama Y, Sugita K, Katayama H.

Ann Hum Genet. 2008 Mar;72(Pt 2):193-204. doi: 10.1111/j.1469-1809.2007.00415.x.

10.

High divergence in primate-specific duplicated regions: human and chimpanzee chorionic gonadotropin beta genes.

Hallast P, Saarela J, Palotie A, Laan M.

BMC Evol Biol. 2008 Jul 7;8:195. doi: 10.1186/1471-2148-8-195.

11.

Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion.

Cuscó I, Corominas R, Bayés M, Flores R, Rivera-Brugués N, Campuzano V, Pérez-Jurado LA.

Genome Res. 2008 May;18(5):683-94. doi: 10.1101/gr.073197.107.

12.

Evolutionary biology. Relative differences: the myth of 1%.

Cohen J.

Science. 2007 Jun 29;316(5833):1836. No abstract available.

PMID:
17600195
13.

Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisons.

Kehrer-Sawatzki H, Cooper DN.

Hum Mutat. 2007 Feb;28(2):99-130. Review.

PMID:
17024666
14.
15.

Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions.

Steinmann K, Kluwe L, Cooper DN, Brems H, De Raedt T, Legius E, Mautner VF, Kehrer-Sawatzki H.

Eur J Hum Genet. 2008 May;16(5):572-80. doi: 10.1038/sj.ejhg.5202002.

16.

Structural variation in the human genome.

Feuk L, Carson AR, Scherer SW.

Nat Rev Genet. 2006 Feb;7(2):85-97. Review.

PMID:
16418744
17.
18.

A comprehensive analysis of common copy-number variations in the human genome.

Wong KK, deLeeuw RJ, Dosanjh NS, Kimm LR, Cheng Z, Horsman DE, MacAulay C, Ng RT, Brown CJ, Eichler EE, Lam WL.

Am J Hum Genet. 2007 Jan;80(1):91-104.

19.

Structural divergence between the human and chimpanzee genomes.

Kehrer-Sawatzki H, Cooper DN.

Hum Genet. 2007 Feb;120(6):759-78. Review.

PMID:
17066299
20.

Copy-number variation and association studies of human disease.

McCarroll SA, Altshuler DM.

Nat Genet. 2007 Jul;39(7 Suppl):S37-42. Review.

PMID:
17597780
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