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Common genetic variants, acting additively, are a major source of risk for autism
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
