24163246Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Wellcome Trust Case Control Consortium, Sklar P, Hultman C, Pato C, Pato M, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Kirov GHuman molecular geneticsChromosome Deletion; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Cytoskeletal Proteins; Excitatory Amino Acid Transporter 3; Gene Duplication; SchizophreniaDNA Copy Number Variations; Female; Gene Deletion; Gene Dosage; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Humans; MaleCNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Hum Mol Genet. 2014 Mar 15; 23(6):1669-76.Hum Mol Genet2013-10-26T00:00:002013CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.prns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:hasSubjectAreaMajorTopicListhas major subject area listprns:hasSubjectAreaMinorTopicListhas minor subject area listprns:informationResourceReferenceinformation resource referenceprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAuthorshipvivo:hasSubjectAreahas subject areaInformation Resourcevivo:informationResourceInAuthorshipauthorsvivo:linkedInformationResourcelinked information resourcerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptD002878Anatomy491000.96087Chromosomes, Human, Pair 1D002872Disorders872280.920654Chromosome DeletionD005260Physiology1992444050.191184FemaleD006801Living Beings2262862810.130064HumansD014644Phenomena29413490.59631Genetic VariationD008297Physiology1931408600.201635MaleD020440Physiology481250.917406Gene DuplicationD017353Physiology1973280.888135Gene DeletionD056726DisordersProcedures1362940.856545Genetic Association StudiesD012559Disorders594640.753769SchizophreniaD056915Physiology991710.89912DNA Copy Number VariationsD018628Concepts & Ideas1102070.920358Gene DosageD002885Anatomy47790.97712Chromosomes, Human, Pair 16D003598Chemicals & Drugs962220.89473Cytoskeletal ProteinsD020022Physiology39922670.521997Genetic Predisposition to DiseaseD050580Chemicals & Drugs450.998029Excitatory Amino Acid Transporter 3Authorship 685010.2427760.2427761authors10.2516has subject area