Global increases in both common and rare copy number load associated with autism-Reference-Cited by-同舟云学术

Global increases in both common and rare copy number load associated with autism

Published:2013-03-27 Issue:14 Volume:22 Page:2870-2880
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Girirajan Santhosh,Johnson Rebecca L.,Tassone Flora,Balciuniene Jorune,Katiyar Neerja,Fox Keolu,Baker Carl,Srikanth Abhinaya,Yeoh Kian Hui,Khoo Su Jen,Nauth Therese B.,Hansen Robin,Ritchie Marylyn,Hertz-Picciotto Irva,Eichler Evan E.,Pessah Isaac N.,Selleck Scott B.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/22/14/2870/17259489/ddt136.pdf

Reference63 articles.

1. CNVs: harbingers of a rare variant revolution in psychiatric genetics;Malhotra;Cell,2012

2. Patterns and rates of exonic de novo mutations in autism spectrum disorders;Neale;Nature,2012

3. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations;O'Roak;Nat. Genet.,2011

4. De novo mutations revealed by whole-exome sequencing are strongly associated with autism;Sanders;Nature,2012

5. De novo gene disruptions in children on the autistic spectrum;Iossifov;Neuron,2012

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