Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts-Reference-Cited by-同舟云学术

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

Published:2012-10-09 Issue:10 Volume:18 Page:1090-1095
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Moreno-De-Luca D,Sanders S J,Willsey A J,Mulle J G,Lowe J K,Geschwind D H,State M W,Martin C L,Ledbetter D H

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://www.nature.com/articles/mp2012138.pdf

Reference29 articles.

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3. Betancur C . Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting. Brain Res 2011; 1380: 42–77.

4. Geschwind DH, Levitt P . Autism spectrum disorders: developmental disconnection syndromes. Curr Opin Neurobiol 2007; 17: 103–111.

5. Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010; 466: 368–372.

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