Simons Simplex Collection

Adaptive behavior profiles of intellectually gifted children with autism spectrum disorder.

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.

How rare and common risk variation jointly affect liability for autism spectrum disorder.

Oligogenic combinations of rare variants influence specific phenotypes in complex disorders.

Genetic counseling as preventive intervention: Toward individual specification of transgenerational autism risk.

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.

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