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dc.contributor.authorMORRIS, DEREK
dc.contributor.authorDONOHOE, GARY (JAMES)
dc.contributor.authorGILL, MICHAEL
dc.contributor.authorCORVIN, AIDEN PETER
dc.date.accessioned2013-08-08T08:55:55Z
dc.date.available2013-08-08T08:55:55Z
dc.date.issued2012
dc.date.submitted2012en
dc.identifier.citationDerks EM, Vorstman JA, Ripke S, Kahn RS, Schizophrenia Psychiatric Genomic Consortium, Ophoff RA, Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis., PloS one, 7, 6, 2012, e37852en
dc.identifier.otherY
dc.identifier.urihttp://hdl.handle.net/2262/66922
dc.descriptionPUBLISHEDen
dc.description.abstractThe presence of subclinical levels of psychosis in the general population may imply that schizophrenia is the extreme expression of more or less continuously distributed traits in the population. In a previous study, we identified five quantitative measures of schizophrenia (positive, negative, disorganisation, mania, and depression scores). The aim of this study is to examine the association between a direct measure of genetic risk of schizophrenia and the five quantitative measures of psychosis. Estimates of the log of the odds ratios of case/control allelic association tests were obtained from the Psychiatric GWAS Consortium (PGC) (minus our sample) which included genome-wide genotype data of 8,690 schizophrenia cases and 11,831 controls. These data were used to calculate genetic risk scores in 314 schizophrenia cases and 148 controls from the Netherlands for whom genotype data and quantitative symptom scores were available. The genetic risk score of schizophrenia was significantly associated with case-control status (p , 0.0001). In the case-control sample, the five psychosis dimensions were found to be significantly associated with genetic risk scores; the correlations ranged between.15 and.27 (all p , .001). However, these correlations were not significant in schizophrenia cases or controls separately. While this study confirms the presence of a genetic risk for schizophrenia as categorical diagnostic trait, we did not find evidence for the genetic risk underlying quantitative schizophrenia symptom dimensions. This does not necessarily imply that a genetic basis is nonexistent, but does suggest that it is distinct from the polygenic risk score for schizophreniaen
dc.description.sponsorshipOver 40 United States National Institutes of Health grants and similar numbers of government grants from other countries, along with substantial private and foundation support, enabled this work. We greatly appreciate the sustained efforts of T. Lehner (National Institute of Mental Health) on behalf of the Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium (PGC). Dr. E.M. Derks is supported by the Netherlands Scientific Organ ization (NWO; project number 451-080-010). Statistical analyses were carried out on the Genetic Cluster Computer (http://www.geneticcluster.org) which is financially supported by the Netherlands Scientific Organization (NWO 480-05-003). The funders had no role in study design, data collection and analysis, decis ion to publish, or preparation of the manuscripten
dc.format.extente37852en
dc.language.isoenen
dc.relation.ispartofseriesPloS one;
dc.relation.ispartofseries7;
dc.relation.ispartofseries6;
dc.rightsYen
dc.subjectschizophreniaen
dc.subject.lcshschizophreniaen
dc.titleInvestigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/acorvin
dc.identifier.peoplefinderurlhttp://people.tcd.ie/morrisdw
dc.identifier.peoplefinderurlhttp://people.tcd.ie/donoghug
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mgill
dc.identifier.rssinternalid80560


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