Article

A Burden of Rare Copy Number Variants in Obsessive-Compulsive Disorder

2024-01-03

Abstract excerpt

<title>Abstract</title> <p>Current genetic research on obsessive-compulsive disorder (OCD) supports contributions to risk specifically from common single nucleotide variants (SNVs), along with rare coding SNVs and small insertion-deletions (indels). The contribution to OCD risk from large, rare copy number variants (CNVs), however, has not been formally assessed at a similar scale. Here we describe an analysis of...

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Literature Corpus work: 28f90519-f9d3-521b-af82-21bd1bad384a
DOI: 10.21203/rs.3.rs-3749504/v1

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