Simons Simplex Collection

Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functions.

The impact of birth order on language development in autistic children from Simplex families.

Rates of contributory de novo mutation in high and low-risk autism families.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders.

Advancing methodologies to improve RRB outcome measures in autism research: Evaluation of the RBS-R.

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.

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