Last Updated: 09/26/2026
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Found 11 publications
Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.
Journal: Science (New York, N.Y.)
Published: August 27, 2026
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders.
Journal: medRxiv : the preprint server for health sciences
Published: November 24, 2025
Whole-exome sequencing in individuals with obsessive-compulsive disorder and chronic tic disorders identifies 36 large-effect risk genes.
Journal: Nature neuroscience
Published: October 08, 2025
Convergence of autism proteins at the cilium.
Journal: bioRxiv : the preprint server for biology
Published: December 16, 2024
Autism genes converge on microtubule biology and RNA-binding proteins during excitatory neurogenesis.
Journal: bioRxiv : the preprint server for biology
Published: January 08, 2024
Pleiotropy of autism-associated chromatin regulators.
Journal: Development (Cambridge, England)
Published: December 07, 2022
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD.
Journal: Nature communications
Published: September 29, 2022
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.
Journal: Nature reviews. Neuroscience
Published: February 18, 2022
Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.
Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
Published: May 09, 2020
Showing 1-11 of 11
Last Updated: 09/26/2026