De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

Schizophrenia is a serious psychiatric disorder with a broadly undiscovered genetic etiology. Recent studies of de novo mutations (DNMs) in schizophrenia and autism have reinforced the hypothesis that rare genetic variation contributes to risk. We carried out exome sequencing on 57 trios with sporad...

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Bibliographic Details
Published in:Molecular psychiatry Vol. 19; no. 6; pp. 652 - 658
Main Authors: McCarthy, S E, Gillis, J, Kramer, M, Lihm, J, Yoon, S, Berstein, Y, Mistry, M, Pavlidis, P, Solomon, R, Ghiban, E, Antoniou, E, Kelleher, E, O'Brien, C, Donohoe, G, Gill, M, Morris, D W, McCombie, W R, Corvin, A
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 01.06.2014
Nature Publishing Group
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ISSN:1359-4184, 1476-5578, 1476-5578
Online Access:Get full text
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