MED13L-related disorder characterized by severe motor speech impairment.
Research Articles
Decomposition of phenotypic heterogeneity in autism reveals distinct and coherent genetic programs.
Human-specific gene expansions contribute to brain evolution.
Agreement of parent-reported cognitive level with standardized measures among children with autism spectrum disorder.
Evaluating causal psychological models: A study of language theories of autism using a large sample.
Multi-ancestry phenome-wide association of complement component 4 variation with psychiatric and brain phenotypes in youth.
Profiles of circumscribed interests in autistic youth.
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
Cross-replicating findings on unique motor impairments of children with ASD using confirmatory factor analysis and a novel SPARK study sample.
The female protective effect against autism spectrum disorder.
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