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Works
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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Functional impact of global rare copy number variation in autism spectrum disorders
Individual common variants exert weak effects on the risk for autism spectrum disorders
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3
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
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
