Literature DB >> 15838535

Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population.

P A Thomson1, N R Wray, J K Millar, K L Evans, S Le Hellard, A Condie, W J Muir, D H R Blackwood, D J Porteous.   

Abstract

The Translin-associated factor X/Disrupted in Schizophrenia 1 (TRAX/DISC) region was first implicated as a susceptibility locus for schizophrenia by analysis of a large Scottish family in which a t(1;11) translocation cosegregates with schizophrenia, bipolar disorder and recurrent major depression. We now report evidence for association between bipolar disorder and schizophrenia and this locus in the general Scottish population. A systematic study of linkage disequilibrium in a representative sample of the Scottish population was undertaken across the 510 kb of TRAX and DISC1. SNPs representing each haplotype block were selected for case-control association studies of both schizophrenia and bipolar disorder. Significant association with bipolar disorder in women P=0.00026 (P=0.0016 in men and women combined) was detected in a region of DISC1. This same region also showed nominally significant association with schizophrenia in both men and women combined, P=0.0056. Two further regions, one in TRAX and the second in DISC1, showed weaker evidence for sex-specific associations of individual haplotypes with bipolar disorder in men and women respectively, P<0.01. Only the association between bipolar women and DISC1 remained significant after correction for multiple testing. This result provides further supporting evidence for DISC1 as a susceptibility factor for both bipolar disorder and schizophrenia, consistent with the diagnoses in the original Scottish translocation family.

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Year:  2005        PMID: 15838535     DOI: 10.1038/sj.mp.4001669

Source DB:  PubMed          Journal:  Mol Psychiatry        ISSN: 1359-4184            Impact factor:   15.992


  51 in total

Review 1.  Genes and schizophrenia: beyond schizophrenia: the role of DISC1 in major mental illness.

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Journal:  Schizophr Bull       Date:  2006-05-12       Impact factor: 9.306

2.  An odor-specific threshold deficit implicates abnormal cAMP signaling in youths at clinical risk for psychosis.

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Review 3.  Imaging genomics and response to treatment with antipsychotics in schizophrenia.

Authors:  Giuseppe Blasi; Alessandro Bertolino
Journal:  NeuroRx       Date:  2006-01

4.  Meta-analysis of 12 genomic studies in bipolar disorder.

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Journal:  J Mol Neurosci       Date:  2007       Impact factor: 3.444

Review 5.  [Correlations between risk gene variants for schizophrenia and brain structure anomalies].

Authors:  T Nickl-Jockschat; M Rietschel; T Kircher
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6.  Addictions biology: haplotype-based analysis for 130 candidate genes on a single array.

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7.  Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging.

Authors:  Kristin K Nicodemus; Joseph H Callicott; Rachel G Higier; Augustin Luna; Devon C Nixon; Barbara K Lipska; Radhakrishna Vakkalanka; Ina Giegling; Dan Rujescu; David St Clair; Pierandrea Muglia; Yin Yao Shugart; Daniel R Weinberger
Journal:  Hum Genet       Date:  2010-04       Impact factor: 4.132

8.  A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder.

Authors:  Jaime M Williams; Tyler F Beck; David M Pearson; Monica B Proud; Sau Wai Cheung; Daryl A Scott
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

9.  Positive association of the pericentrin (PCNT) gene with major depressive disorder in the Japanese population.

Authors:  Shusuke Numata; Jun-Ichi Iga; Masahito Nakataki; Shin'ya Tayoshi; Toshihito Tanahashi; Mitsuo Itakura; Shu-Ichi Ueno; Tetsuro Ohmori
Journal:  J Psychiatry Neurosci       Date:  2009-05       Impact factor: 6.186

10.  Association of variants in DISC1 with psychosis-related traits in a large population cohort.

Authors:  Liisa Tomppo; William Hennah; Jouko Miettunen; Marjo-Riitta Järvelin; Juha Veijola; Samuli Ripatti; Päivi Lahermo; Dirk Lichtermann; Leena Peltonen; Jesper Ekelund
Journal:  Arch Gen Psychiatry       Date:  2009-02
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