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Items: 1 to 20 of 47

1.

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.

2.

[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
3.

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. Epub 2009 Mar 11. Review.

PMID:
19287153
4.

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
5.

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.

6.
7.

Germline copy number variation in control populations.

Al-Sukhni W, Gallinger S.

Cytogenet Genome Res. 2008;123(1-4):211-23. doi: 10.1159/000184711. Epub 2009 Mar 11. Review.

PMID:
19287158
8.

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.

Lee C, Iafrate AJ, Brothman AR.

Nat Genet. 2007 Jul;39(7 Suppl):S48-54. Review.

PMID:
17597782
9.

Copy number variations and cancer susceptibility.

Shlien A, Malkin D.

Curr Opin Oncol. 2010 Jan;22(1):55-63. doi: 10.1097/CCO.0b013e328333dca4. Review.

PMID:
19952747
10.

Large-scale copy number variants (CNVs) detected in different ethnic human populations.

Takahashi N, Satoh Y, Kodaira M, Katayama H.

Cytogenet Genome Res. 2008;123(1-4):224-33. doi: 10.1159/000184712. Epub 2009 Mar 11. Review.

PMID:
19287159
11.

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.

12.

[Copy number variations in the human genome: their mutational mechanisms and roles in diseases].

Du RQ, Jin L, Zhang F.

Yi Chuan. 2011 Aug;33(8):857-69. Review. Chinese.

PMID:
21831802
13.

Copy number variation in the cattle genome.

Liu GE, Bickhart DM.

Funct Integr Genomics. 2012 Nov;12(4):609-24. doi: 10.1007/s10142-012-0289-9. Epub 2012 Jul 13. Review.

PMID:
22790923
14.

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.

15.

Detection and characterization of copy number variation in autism spectrum disorder.

Marshall CR, Scherer SW.

Methods Mol Biol. 2012;838:115-35. doi: 10.1007/978-1-61779-507-7_5. Review.

PMID:
22228009
16.

Pharmacogenetics: technologies to detect copy number variations.

Dhawan D, Padh H.

Curr Opin Mol Ther. 2009 Dec;11(6):670-80. Review.

PMID:
20072944
17.

The evolutionary significance of copy number variation in the human genome.

Perry GH.

Cytogenet Genome Res. 2008;123(1-4):283-7. doi: 10.1159/000184719. Epub 2009 Mar 11. Review.

18.

The impact of human copy number variation on a new era of genetic testing.

Choy KW, Setlur SR, Lee C, Lau TK.

BJOG. 2010 Mar;117(4):391-8. doi: 10.1111/j.1471-0528.2009.02470.x. Epub 2010 Jan 26. Review.

19.

Origins and breakpoint analyses of copy number variations: up close and personal.

van Binsbergen E.

Cytogenet Genome Res. 2011;135(3-4):271-6. doi: 10.1159/000330267. Epub 2011 Aug 12. Review.

PMID:
21846967
20.

Structural variation in the human genome: the impact of copy number variants on clinical diagnosis.

Rodriguez-Revenga L, Mila M, Rosenberg C, Lamb A, Lee C.

Genet Med. 2007 Sep;9(9):600-6. Review.

PMID:
17873648
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