Pathways to understanding psychosis through rare – 22q11.2DS - and common variants. (June 2021)

• Record Type: Journal Article
• Authors: Gur, Raquel E; Roalf, David R; Alexander-Bloch, Aaron; McDonald-McGinn, Donna M; Gur, Ruben C
• Is Part Of: Current opinion in genetics & development. Volume 68(2021)
• Page Start: 35
• Page End: 40
• Publication Date: 2021-06
• Subjects: Genetics -- Periodicals; Developmental biology -- Periodicals; Developmental genetics -- Periodicals; 576.5
• DOI: 10.1016/j.gde.2021.01.007
• Languages: English
• ISSNs: 0959-437X

Abstract

Abstract : The 22q11.2 Deletion Syndrome has significant impact on brain and behavior, with about 25% of individuals developing schizophrenia. The condition offers a model for prospective studies on the emergence of psychosis and advancing mechanistic hypotheses on gene-environment interactions, with magnified power for examining genome-phenome association. Here, we highlight findings that build on the International 22q11.2 Brain and Behavior Consortium and relate to several key domains in the study of psychosis-risk and schizophrenia. We examine neurocognition, olfaction and neuroimaging data that indicate similar impairment patterns in this rare syndrome and idiopathic presentation of schizophrenia. We conclude that the converging paradigms, studying psychosis dimensionally in rare and common variants samples, provide complementary approaches that will propel precision medicine in psychiatry.