Simons Simplex Collection

The network structure of irritability and aggression in individuals with autism spectrum disorder.

Exploring the familial role of social responsiveness differences between savant and non-savant children with autism.

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism.

Beliefs in vaccine as causes of autism among SPARK cohort caregivers.

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders.

Transcriptome-wide transmission disequilibrium analysis identifies novel risk genes for autism spectrum disorder.

Elevated polygenic burden for autism spectrum disorder is associated with the broad autism phenotype in mothers of individuals with autism spectrum disorder.

De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism.

Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders

Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission.

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