A genome-wide scan for common alleles affecting risk for autism.

Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the Autism Genome Project (AGP) Consortium genotyped 1558 rigorously defined ASD fa...

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Bibliographic Details
Main Authors:	Anney, R, Klei, L, Pinto, D, Regan, R, Conroy, J, Magalhaes, T, Correia, C, Abrahams, B, Sykes, N, Pagnamenta, A, Almeida, J, Bacchelli, E, Bailey, A, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bölte, S, Bolton, P, Bourgeron, T, Brennan, S, Brian, J, Carson, A, Casallo, G, Casey, J
Format:	Journal article
Language:	English
Published:	2010

A genome-wide scan for common alleles affecting risk for autism.

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