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Functional impact of global rare copy number variation in autism spectrum disorders
Common genetic variants, acting additively, are a major source of risk for autism
Individual common variants exert weak effects on the risk for autism spectrum disorders
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
A genome-wide scan for common alleles affecting risk for autism
