Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1

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Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1 is …
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scholarly articleQ13442814

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P6179Dimensions Publication ID1010439723
P356DOI10.1186/1471-2350-15-2
P3181OpenCitations bibliographic resource ID33724
P932PMC publication ID3901032
P698PubMed publication ID24387768
P5875ResearchGate publication ID259586127

P50authorPeter McGuffinQ7175787
Anne FarmerQ16151236
Andrew McQuillinQ37652167
Jo KnightQ39065126
Pingzhao HuQ39652071
Georgina M. HosangQ44547539
Sarah Cohen-WoodsQ44547557
Federica TozziQ47502259
P2093author name stringWei Xu
Abdul Noor
John B Vincent
James L Kennedy
Qian Chen
Hugh M D Gurling
Pierandrea Muglia
Vincenzo De Luca
John Strauss
Sagar V Parikh
Julia Forte
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Putative psychosis genes in the prefrontal cortex: combined analysis of gene expression microarraysQ30851360
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Darier's disease cosegregating with affective disorderQ72442306
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PP2A-Bgamma subunit and KCNQ2 K+ channels in bipolar disorderQ33245065
Genetics of bipolar disorder.Q33721526
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CSMD1 is a novel multiple domain complement-regulatory protein highly expressed in the central nervous system and epithelial tissuesQ34503418
PDE4B polymorphisms and decreased PDE4B expression are associated with schizophreniaQ34768445
Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13.Q34828678
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Genome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: what have we learnt?Q37938511
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Opportunities for psychiatry from genetic findings.Q40880501
A secreted complement-control-related protein ensures acetylcholine receptor clustering.Q43268892
The 5HT1Dbeta receptor gene in bipolar disorder: a family-based association studyQ43737582
A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT systemQ43754027
Sample size requirements for matched case‐control studies of gene–environment interactionQ43848305
Early age at onset as a risk factor for poor outcome of bipolar disorderQ44295348
Validation of schizophrenia-associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR-137 targetsQ45263643
Candidate gene association analysis for a quantitative trait, using parent-offspring trios.Q45935639
Association study of PDE4B gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samplesQ46058975
Admixture analysis of age at onset in bipolar disorderQ47379618
Reduced neuropeptide Y mRNA expression in the prefrontal cortex of subjects with bipolar disorderQ48103303
PPP2R2C, a gene disrupted in autosomal dominant intellectual disabilityQ48140457
Brain-derived neurotrophic factor (BDNF) gene and rapid-cycling bipolar disorder: family-based association studyQ48407989
P4510describes a project that usesgenome-wide association studyQ1098876
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectbipolar disorderQ131755
genome-wide association studyQ1098876
P304page(s)2
P577publication date2014-01-01
P1433published inBMC Medical GeneticsQ15759918
P1476titleGenome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1
P478volume15

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