Simons Simplex Collection

Utility of the Social Communication Questionnaire-Current and Social Responsiveness Scale as teacher-report screening tools for autism spectrum disorders.

De novo gene disruptions in children on the autistic spectrum.

Common genetic variants, acting additively, are a major source of risk for autism.

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.

A multisite study of the clinical diagnosis of different autism spectrum disorders.

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorder.

Predicting improvement in social-communication symptoms of autism spectrum disorders using retrospective treatment data.

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

The behavioral phenotype in MeCP2 duplication syndrome: A comparison to idiopathic autism.

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