Simons Simplex Collection

Dopaminergic gene dosage reveals distinct biological partitions between autism and developmental delay as revealed by complex network analysis and machine learning approaches.

Similar rates of deleterious copy number variants in early-onset psychosis and autism spectrum disorder.

Bias in measurement of autism symptoms by spoken language level and non-verbal mental age in minimally verbal children with neurodevelopmental disorders.

Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functions.

Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.

Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity.

The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects

Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.

An epigenetically distinct subset of children with autism spectrum disorder resulting from differences in blood cell composition.

Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.

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