Structural and functional brain alterations revealed by neuroimaging in CNV carriers

Curr Opin Genet Dev. 2021 Jun:68:88-98. doi: 10.1016/j.gde.2021.03.002. Epub 2021 Mar 31.

Abstract

Copy Number Variants (CNVs) are associated with elevated rates of neuropsychiatric disorders. A 'genetics-first' approach, involving the CNV effects on the brain, irrespective of clinical symptomatology, allows investigation of mechanisms underlying neuropsychiatric disorders in the general population. Recent years have seen an increasing number of larger multisite neuroimaging studies investigating the effect of CNVs on structural and functional brain endophenotypes. Alterations overlap with those found in idiopathic psychiatric conditions but effect sizes are twofold to fivefold larger. Here we review new CNV-associated structural and functional brain alterations and outline the future of neuroimaging genomics research, with particular emphasis on developing new resources for the study of high-risk CNVs and rare genomic variants.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Brain / physiology*
  • DNA Copy Number Variations*
  • Endophenotypes
  • Genetic Predisposition to Disease*
  • Genome-Wide Association Study
  • Genomics
  • Humans
  • Mental Disorders / genetics*
  • Neuroimaging / methods*