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Abnormal speech motor control in individuals with 16p11.2 deletions.

Cellular phenotypes in human iPSC-derived neurons from a genetic model of autism spectrum disorder.

Incorporating social media into your support tool box: Points to consider from genetics-based communities.

Brain MR imaging findings and associated outcomes in carriers of the reciprocal copy number variation at 16p11.2.

Behavior and sensory interests questionnaire: Validation in a sample of children with autism spectrum disorder and other developmental disability.

Simons Variation in Individuals Project (Simons VIP): A genetics-first approach to studying autism spectrum and related neurodevelopmental disorders.

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

Opposing brain differences in 16p11.2 deletion and duplication carriers.

Aberrant white matter microstructure in children with 16p11.2 deletions.

Eating in the absence of hunger but not loss of control behaviors are associated with 16p11.2 deletions.