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.

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

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

SMASH, a fragmentation and sequencing method for genomic copy number analysis.

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