Simons Simplex Collection

Clinical phenotype of ASD-associated DYRK1A haploinsufficiency.

TiSAn: Estimating tissue specific effects of coding and non-coding variants.

Children with autism spectrum disorder who improve with fever: Insights from the Simons Simplex Collection.

Functional significance of rare neuroligin 1 variants found in autism.

Exonic mosaic mutations contribute risk for autism spectrum disorder.

Gene disrupting mutations associated with regression in autism spectrum disorder.

Interactive effects of prenatal antidepressant exposure and likely gene disrupting mutations on the severity of autism spectrum disorder

Post-zygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations.

Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.

Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism.

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