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Common genetic variants, acting additively, are a major source of risk for autism
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Between a ROC and a hard place: decision making and making decisions about using the SCQ.
Individual common variants exert weak effects on the risk for autism spectrum disorders
Convergence of genes and cellular pathways dysregulated in 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
Combining information from multiple sources in the diagnosis of autism spectrum disorders
