Association at SYNE1 in both bipolar disorder and recurrent major depression

scientific article

Association at SYNE1 in both bipolar disorder and recurrent major depression is …
instance of (P31):
scholarly articleQ13442814
meta-analysisQ815382

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P356DOI10.1038/MP.2012.48
P698PubMed publication ID22565781
P5875ResearchGate publication ID224918200

P50authorDetelina GrozevaQ37650671
Jennifer L. MoranQ37651649
Nick CraddockQ18685542
Katherine Gordon-SmithQ29998782
Michael C O'DonovanQ30410265
P2093author name stringL Jones
M J Owen
A Farmer
P McGuffin
I R Jones
P Sklar
M Hamshere
L Forty
S Purcell
E K Green
E Russell
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Nesprins: intracellular scaffolds that maintain cell architecture and coordinate cell function?Q36161599
Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccoloQ37280609
Genetics of bipolar disorder: successful start to a long journeyQ37368587
SCAN. Schedules for Clinical Assessment in NeuropsychiatryQ37929723
Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrityQ40087014
A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT systemQ43754027
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundariesQ45386905
Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxiaQ48341636
Concurrent validity of the OPCRIT diagnostic system. Comparison of OPCRIT diagnoses with consensus best-estimate lifetime diagnosesQ52889404
Design of Case-controls Studies with Unscreened ControlsQ58132458
Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposisQ84096029
The Kraepelinian dichotomy - going, going... but still not goneQ22241683
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsQ24550675
The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophreniaQ24619976
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderQ24634497
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorderQ24655630
PLINK: a tool set for whole-genome association and population-based linkage analysesQ24677407
The Bipolar Affective Disorder Dimension Scale (BADDS)--a dimensional scale for rating lifetime psychopathology in bipolar spectrum disordersQ24793900
Genome-wide association study identifies five new schizophrenia lociQ28248384
Common polygenic variation contributes to risk of schizophrenia and bipolar disorderQ28250609
Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic riskQ28303293
Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.Q29417043
Identification of loci associated with schizophrenia by genome-wide association and follow-upQ29417130
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4Q29417143
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.Q29417150
Genetics of bipolar disorder.Q33721526
Gene expression and genetic variation data implicate PCLO in bipolar disorderQ33780246
Family, twin, and adoption studies of bipolar disorderQ34274776
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectbipolar disorderQ131755
P304page(s)614-617
P577publication date2012-05-08
P1433published inMolecular PsychiatryQ6895973
P1476titleAssociation at SYNE1 in both bipolar disorder and recurrent major depression
P478volume18

Reverse relations

cites work (P2860)
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