Your browser doesn't support javascript.
loading
Structural and functional brain alterations revealed by neuroimaging in CNV carriers.
Moreau, Clara A; Ching, Christopher Rk; Kumar, Kuldeep; Jacquemont, Sebastien; Bearden, Carrie E.
Afiliação
  • Moreau CA; Sainte-Justine Hospital Research Center, Montreal, Canada; Department of Pediatrics, University of Montreal, Montreal, Canada; Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montréal, Canada; Human Genetics and Cognitive Functions, CNRS UMR 3571, Université de Paris, Insti
  • Ching CR; Imaging Genetics Center, USC Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine of the University of Southern California, USA.
  • Kumar K; Sainte-Justine Hospital Research Center, Montreal, Canada.
  • Jacquemont S; Sainte-Justine Hospital Research Center, Montreal, Canada; Department of Pediatrics, University of Montreal, Montreal, Canada. Electronic address: sebastien.jacquemont@umontreal.ca.
  • Bearden CE; Semel Institute for Neuroscience and Human Behavior, Departments of Psychiatry and Biobehavioral Sciences and Psychology, University of California, Los Angeles, USA. Electronic address: CBearden@mednet.ucla.edu.
Curr Opin Genet Dev ; 68: 88-98, 2021 06.
Article em En | MEDLINE | ID: mdl-33812299
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Predisposição Genética para Doença / Variações do Número de Cópias de DNA / Neuroimagem / Transtornos Mentais Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Predisposição Genética para Doença / Variações do Número de Cópias de DNA / Neuroimagem / Transtornos Mentais Idioma: En Ano de publicação: 2021 Tipo de documento: Article