Simons Simplex Collection

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.

Nonverbal and verbal cognitive discrepancy profiles in autism spectrum disorders: Influence of age and gender.

Expression of the broad autism phenotype in simplex autism families from the Simons Simplex Collection.

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.

Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.

Comparison of fecal microbiota in children with autism spectrum disorders and neurotypical siblings in the Simons Simplex Collection.

Loss of delta-catenin function in severe autism.

An autism-linked mutation disables phosphorylation control of UBE3A.

Patterns of risk for multiple co-occurring medical conditions replicate across distinct cohorts of children with autism spectrum disorder.

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