Simons Simplex Collection

Peripheral blood gene expression signature differentiates children with autism from unaffected siblings.

Transmission disequilibrium of small CNVs in simplex autism.

Rare complete knockouts in humans: Population distribution and significant role in autism spectrum disorders.

Predicting language and social outcomes at age 5 for later-born siblings of children with autism spectrum disorders.

A higher mutational burden in females supports a “female protective model” in neurodevelopmental disorders.

Behavioral and cognitive characteristics of females and males with autism in the Simons Simplex Collection.

Reducing indel calling errors in whole genome and exome sequencing data.

Developmental regression among children with autism spectrum disorders: Onset, duration, and effects on functional outcomes.

Rare-variant extensions of the transmission disequilibrium test: Application to autism exome sequence data.

The contribution of de novo coding mutations to autism spectrum disorder.

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