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dc.contributor.authorCORVIN, AIDENen
dc.contributor.authorHERON, ELIZABETHen
dc.contributor.authorGILL, MICHAELen
dc.contributor.authorDONOHOE, GARYen
dc.contributor.authorANNEY, RICHARDen
dc.contributor.authorGALLAGHER, LOUISEen
dc.contributor.authorMORRIS, DEREKen
dc.contributor.authorTROPEA, DANIELAen
dc.contributor.authorKENNY, ELAINEen
dc.date.accessioned2016-01-19T13:20:28Z
dc.date.available2016-01-19T13:20:28Z
dc.date.issued2014en
dc.date.submitted2014en
dc.identifier.citationKenny EM, Cormican P, Furlong S, Heron E, Kenny G, Fahey C, Kelleher E, Ennis S, Tropea D, Anney R, Corvin AP, Donohoe G, Gallagher L, Gill M, Morris DW, Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders., Molecular psychiatry, 19, 2014, 872-879en
dc.identifier.issn1359-4184en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/75625
dc.descriptionPUBLISHEDen
dc.format.extent872-879en
dc.language.isoenen
dc.relation.ispartofseriesMolecular psychiatryen
dc.relation.ispartofseries19en
dc.rightsYen
dc.subjectSchizophreniaen
dc.subjectAutismen
dc.titleExcess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/acorvinen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/anneyren
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mgillen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/tropeaden
dc.identifier.peoplefinderurlhttp://people.tcd.ie/eaheronen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/donoghugen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/morrisdwen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/kennyelen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/lgallaghen
dc.identifier.rssinternalid91497en
dc.identifier.doihttp://dx.doi.org/10.1038/mp.2013.127en
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeGenes & Societyen
dc.subject.TCDThemeNeuroscienceen
dc.identifier.orcid_id0000-0001-6717-4089en


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