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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Vydáno v:	Molecular psychiatry Ročník 19; číslo 6; s. 652 - 658
Hlavní autoři:	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
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	London Nature Publishing Group UK 01.06.2014 Nature Publishing Group
Témata:	692/420/2489/144 692/699/476/1373 692/699/476/1799 Adolescent Adult Adult and adolescent clinical studies Autism Autistic Disorder - genetics Behavioral Sciences Biological and medical sciences Biological Psychology Child clinical studies Chromatin Assembly and Disassembly - genetics Chromatin remodeling Codon, Nonsense Cognition Developmental disorders DNA Mutational Analysis Epigenetics Etiology Exome Family Female Gene mutations Gene regulation Genetic aspects Genetic diversity Genetic Predisposition to Disease Genetic research Genetic susceptibility Haploinsufficiency Humans Huwe1 protein Identification and classification immediate-communication Infantile autism Intellectual deficiency Intellectual disabilities Intellectual Disability - genetics Male MeCP2 protein Medical sciences Medicine Medicine & Public Health Mental disorders Methyl-CpG binding protein Middle Aged Mutation Neurodevelopmental disorders Neurosciences Pharmacotherapy Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Schizophrenia Schizophrenia - genetics Transcription Young Adult Psychosis Handicap Autism Chromatin Intellectual deficiency Schizophrenia Genetics Developmental disorder Mutation Mental retardation
ISSN:	1359-4184, 1476-5578, 1476-5578
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