Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample-Reference-Cited by-同舟云学术

Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample

Published:2013-08-13 Issue:11 Volume:18 Page:1178-1184
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Szatkiewicz J P,Neale B M,O'Dushlaine C,Fromer M,Goldstein J I,Moran J L,Chambert K,Kähler A,Magnusson P K E,Hultman C M,Sklar P,Purcell S,McCarroll S A,Sullivan P F^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology

Link

http://www.nature.com/articles/mp201398.pdf

Reference22 articles.

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2. Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J et al. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry 2011; 168: 302–316.

3. Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011; 70: 863–885.

4. Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C et al. A copy number variation morbidity map of developmental delay. Nat Genet 2011; 43: 838–846.

5. Sullivan PF, Daly MJ, O'Donovan M . Genetic architectures of psychiatric disorders: the emerging picture and its implications. Nat Rev Genet 2012; 13: 537–551.

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