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dc.contributor.authorGILL, MICHAELen
dc.contributor.authorCORVIN, AIDENen
dc.contributor.authorMORRIS, DEREKen
dc.date.accessioned2014-11-26T15:28:53Z
dc.date.available2014-11-26T15:28:53Z
dc.date.issued2014en
dc.date.submitted2014en
dc.identifier.citationRees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, Pato M, Genovese G, Levinson D, Duan J, Moy W, Göring HH, Morris D, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Craddock N, Sklar P, Hultman C, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Evidence that duplications of 22q11.2 protect against schizophrenia., Molecular psychiatry, 19, 1, 2014, 37-40en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractA number of large, rare copy number variants (CNVs) are deleterious for neurodevelopmental disorders, but large, rare, protective CNVs have not been reported for such phenotypes. Here we show in a CNV analysis of 47 005 individuals, the largest CNV analysis of schizophrenia to date, that large duplications (1.5-3.0 Mb) at 22q11.2--the reciprocal of the well-known, risk-inducing deletion of this locus--are substantially less common in schizophrenia cases than in the general population (0.014% vs 0.085%, OR=0.17, P=0.00086). 22q11.2 duplications represent the first putative protective mutation for schizophrenia.en
dc.format.extent37-40en
dc.language.isoenen
dc.relation.ispartofseriesMolecular psychiatryen
dc.relation.ispartofseries19en
dc.relation.ispartofseries1en
dc.rightsYen
dc.subjectschizophrenia,en
dc.titleEvidence that duplications of 22q11.2 protect against schizophrenia.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mgillen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/morrisdwen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/acorvinen
dc.identifier.rssinternalid94481en
dc.identifier.doihttp://dx.doi.org/10.1038/mp.2013.156en
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeGenes & Societyen
dc.subject.TCDThemeNeuroscienceen
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.contributor.sponsorGrantNumber08/IN.1/B1916en
dc.identifier.urihttp://hdl.handle.net/2262/72206


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