Journal article
Individual common variants exert weak effects on the risk for autism spectrum disorders
Abstract
While it is apparent that rare variation can play an important role in the genetic architecture of autism spectrum disorders (ASDs), the contribution of common variation to the risk of developing ASD is less clear. To produce a more comprehensive picture, we report Stage 2 of the Autism Genome Project genome-wide association study, adding 1301 ASD families and bringing the total to 2705 families analysed (Stages 1 and 2). In addition to …
Authors
Anney R; Klei L; Pinto D; Almeida J; Bacchelli E; Baird G; Bolshakova N; Bölte S; Bolton PF; Bourgeron T
Journal
Human Molecular Genetics, Vol. 21, No. 21, pp. 4781–4792
Publisher
Oxford University Press (OUP)
Publication Date
November 1, 2012
DOI
10.1093/hmg/dds301
ISSN
0964-6906