Preprints

Noncoding de novo mutations in SCN2A are associated with autism spectrum disorders.

Prematurity and genetic liability for autism spectrum disorder.

Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk.

Single cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism.

Distinct roles of putative excitatory and inhibitory neurons in the macaque inferior temporal cortex in core object recognition behavior.

Reprogramming method does not impact the neuronal differentiation potential of 16p11.2 deletion patient iPSCs.

Developmental molecular controls over arealization of descending cortical motor pathways.

Environmental adversity moderates polygenic score effects on childhood behavioral problems in the United States.

Structural neuroplasticity after sleep loss modifies behavior and requires neurexin and neuroligin.

Autism spectrum disorder trios from consanguineous populations are enriched for rare biallelic variants, identifying 32 new candidate genes.