“Guilt by association” is not competitive with genetic association for identifying autism risk genes.
SPARK
Genetic correlates of phenotypic heterogeneity in autism.
Psychological distress among caregivers raising a child with autism spectrum disorder during the COVID-19 pandemic.
Big data approach to characterize restricted and repetitive behaviors in autism.
Co-occurring attention-deficit/hyperactivity disorder and anxiety disorders differentially affect males and females with autism.
Validation of autism diagnosis and clinical data in the SPARK cohort.
Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Interpreting polygenic score effects in sibling analysis.
De novo variant calling identifies cancer mutation profiles in the 1000 Genomes Project.
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene.
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