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Items: 1 to 20 of 106

1.

Extending genome-wide association studies to copy-number variation.

McCarroll SA.

Hum Mol Genet. 2008 Oct 15;17(R2):R135-42. doi: 10.1093/hmg/ddn282. Review.

PMID:
18852202
2.

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
3.

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.

Weiss LA.

Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Review.

PMID:
19895225
4.

The emerging role of structural variations in common disorders: initial findings and discovery challenges.

Armengol L, Rabionet R, Estivill X.

Cytogenet Genome Res. 2008;123(1-4):108-17. doi: 10.1159/000184698. Epub 2009 Mar 11. Review.

PMID:
19287145
5.
6.

The pursuit of genome-wide association studies: where are we now?

Ku CS, Loy EY, Pawitan Y, Chia KS.

J Hum Genet. 2010 Apr;55(4):195-206. doi: 10.1038/jhg.2010.19. Epub 2010 Mar 19. Review.

PMID:
20300123
7.

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
8.

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
9.

Contribution of Fcgamma receptor IIIA gene 158V/F polymorphism and copy number variation to the risk of ACPA-positive rheumatoid arthritis.

Thabet MM, Huizinga TW, Marques RB, Stoeken-Rijsbergen G, Bakker AM, Kurreeman FA, White SJ, Toes RE, van der Helm-van Mil AH.

Ann Rheum Dis. 2009 Nov;68(11):1775-80. doi: 10.1136/ard.2008.099309. Epub 2008 Nov 19. Review.

PMID:
19019892
10.

Copy number variation of beta-defensins and relevance to disease.

Hollox EJ.

Cytogenet Genome Res. 2008;123(1-4):148-55. doi: 10.1159/000184702. Epub 2009 Mar 11. Review.

PMID:
19287149
11.

Schizophrenia genetics: advancing on two fronts.

Owen MJ, Williams HJ, O'Donovan MC.

Curr Opin Genet Dev. 2009 Jun;19(3):266-70. doi: 10.1016/j.gde.2009.02.008. Epub 2009 Apr 1. Review.

PMID:
19345090
12.

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
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.

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.

15.

The role of DNA copy number variation in schizophrenia.

Tam GW, Redon R, Carter NP, Grant SG.

Biol Psychiatry. 2009 Dec 1;66(11):1005-12. doi: 10.1016/j.biopsych.2009.07.027. Epub 2009 Sep 12. Review.

PMID:
19748074
16.

Chromosome copy number variation and breast cancer risk.

Tchatchou S, Burwinkel B.

Cytogenet Genome Res. 2008;123(1-4):183-7. doi: 10.1159/000184707. Epub 2009 Mar 11. Review.

PMID:
19287154
17.

HIV-1/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5.

Nakajima T, Kaur G, Mehra N, Kimura A.

Cytogenet Genome Res. 2008;123(1-4):156-60. doi: 10.1159/000184703. Epub 2009 Mar 11. Review.

PMID:
19287150
18.

Biostatistical aspects of genome-wide association studies.

Ziegler A, K├Ânig IR, Thompson JR.

Biom J. 2008 Feb;50(1):8-28. doi: 10.1002/bimj.200710398. Review.

PMID:
18217698
19.

Copy number variation in metabolic phenotypes.

Lanktree M, Hegele RA.

Cytogenet Genome Res. 2008;123(1-4):169-75. doi: 10.1159/000184705. Epub 2009 Mar 11. Review.

PMID:
19287152
20.

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