Article
Rare variation illuminates the distinct and pleiotropic genetic architecture of autism across neuropsychiatric traits
2026-08-26
Abstract excerpt
Autism spectrum disorder is a heritable neurodevelopmental condition affecting approximately 3% of children that presents with core behavioral features and a range of possible comorbidities, including intellectual disability. While common variants contribute substantially to autism liability, the discovery of specific autism-associated genes has largely been driven by studies of rare and de novo variants. Many of...
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Identifiers and source
- Literature Corpus work
- 27d02304-96e7-5aec-90ea-ca0efe23f224
- DOI
- 10.64898/2026.08.24.26360398