Simons Simplex Collection

Recurrent de novo mutations implicate novel genes underlying simplex autism risk.

Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.

A framework for the interpretation of de novo mutation in human disease.

NPAS1 represses the generation of specific subtypes of cortical interneurons.

The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder.

Brief report: Impact of child problem behaviors and parental broad autism phenotype traits on substance use among parents of children with ASD.

Soy infant formula and seizures in children with autism: A retrospective study.

Investigation of maternal genotype effects in autism by genome-wide association.

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

No increase in autism associated genetic events in children conceived by assisted reproductive technology.

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