Simons Simplex Collection

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.

De novo variant calling identifies cancer mutation profiles in the 1000 Genomes Project.

Comparing fathers’ and mothers’ perspectives about their child’s autism spectrum disorder.

Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of genetic variants in vivo.

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