Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression-Reference-Cited by-同舟云学术

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Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression

Published:2011-06-16 Issue:18 Volume:20 Page:3632-3641
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Ben-David Eyal,Granot-Hershkovitz Einat,Monderer-Rothkoff Galya,Lerer Elad,Levi Shlomit,Yaari Maya,Ebstein Richard P.,Yirmiya Nurit,Shifman Sagiv

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/20/18/3632/17253304/ddr283.pdf

Reference41 articles.

1. Strong association of de novo copy number mutations with autism;Sebat;Science,2007

2. Functional impact of global rare copy number variation in autism spectrum disorders;Pinto;Nature,2010

3. Challenges in the identification and use of rare disease-associated predisposition variants;Carvajal-Carmona;Curr. Opin. Genet. Dev.,2010

4. Exome sequencing: the sweet spot before whole genomes;Teer;Hum. Mol. Genet.,2010

5. Gene expression in the etiology of schizophrenia;Bray;Schizophr. Bull.,2008

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