Simons Simplex Collection

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.

“Guilt by association” is not competitive with genetic association for identifying autism risk genes.

Genetic correlates of phenotypic heterogeneity in autism.

Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances.

Subgrouping school-aged children with autism spectrum disorder based on co-occurring psychopathology.

A neurogenetic analysis of female autism.

Recent ultra-rare inherited variants implicate new autism candidate risk genes.

De novo human brain enhancers created by single nucleotide mutations.

A method to delineate de novo missense variants across pathways prioritizes genes linked to autism.

Using the big data approach to clarify the structure of restricted and repetitive behaviors across the most commonly used autism spectrum disorder measures.

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