Article

A Survey of Copy Number Variants Associated with Neurodevelopmental Disorders in a Large-Scale, Multi-Ancestry Biobank

2021-06-12

Abstract excerpt

<h4>ABSTRACT</h4> <h4>BACKGROUND</h4> Past clinical genetic studies have identified rare, copy number variants (CNVs) as risk factors for multiple neurodevelopmental disorders (NDD), including autism spectrum disorder and schizophrenia. However, the broad, clinical characterization of these NDD-CNVs in large population cohorts, especially of diverse ancestry, is relatively understudied. We characterized the clinic...

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Literature Corpus work: 5be17b3d-6a04-5d02-9c95-c310af0c3dcf
DOI: 10.1101/2021.06.09.21258554

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