SPARK

Enrichment of a subset of Neanderthal polymorphisms in autistic probands and siblings.

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

Phenotypic and ancestry-related assortative mating in autism.

Return of genetic research results in 21,532 individuals with autism.

Validating motor delays across the developmental coordination disorder-questionnaire and the Vineland adaptive behavior scales (VABS) in children with autism spectrum disorderASD: A SPARK dataset analysis.

Autistic characteristics, cognitive impairment, and sex as predictors of anxiety and depression among autistic youth.

Barriers, motivators and strategies to increase participation in genetic research among Asian and Black families of autistic individuals.

Copy-number variants differ in frequency across genetic ancestry groups.

Machine learning prediction of autism spectrum disorder from a minimal set of medical and background information.

Unveiling the role of IGF1R in autism spectrum disorder: a multi-omics approach to decipher common pathogenic mechanisms in the IGF signaling pathway.