Association of cognitive and adaptive skills with internalizing and externalizing problems in autistic children and adolescents.
Simons Simplex Collection
Open dataset of theory of mind reasoning in early to middle childhood.
Severity of autism spectrum disorder symptoms associated with de novo variants and pregnancy-induced hypertension.
The Genotype and Phenotypes in Families (GPF) platform manages the large and complex data at SFARI.
Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk.
Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
Protocol for the development of joint attention-based subclassification of autism spectrum disorder and validation using multi-modal data.
The contributions of rare inherited and polygenic risk to ASD in multiplex families.
Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders.
VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants.
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