Literature DB >> 19693800

Support of association between BRD1 and both schizophrenia and bipolar affective disorder.

Mette Nyegaard1,2, Jacob E Severinsen1, Thomas D Als3, Anne Hedemand1, Steen Straarup3, Merete Nordentoft4, Andrew McQuillin5, Nicholas Bass5, Jacob Lawrence5, Srinivasa Thirumalai6, Ana C P Pereira5, Radhika Kandaswamy5, Gregory J Lydall5, Pamela Sklar7, Edward Scolnick7, Shaun Purcell7, David Curtis8, Hugh M D Gurling5, Preben B Mortensen9, Ole Mors3, Anders D Børglum1,3.   

Abstract

A recent study published by our group implicated the bromodomain containing protein 1 (BRD1) gene located at chromosome 22q13.33 with schizophrenia (SZ) and bipolar affective disorder (BPD) susceptibility and provided evidence suggesting a possible role for BRD1 in neurodevelopment. The present study reports an association analysis of BRD1 and the neighboring gene ZBED4 using a Caucasian case-control sample from Denmark and England (UK/DK sample: 490 patients with BPD, 527 patients with SZ, and 601 control individuals), and genotypes obtained from a BPD genome wide association (GWA) study of an overlapping English sample comprising 506 patients with BPD and 510 control individuals (UCL sample). In the UK/DK sample we genotyped 11 SNPs in the BRD1 region, of which six showed association with SZ (minimal single marker P-values of 0.0014), including two SNPs that previously showed association in a Scottish population [Severinsen et al. (2006); Mol Psychiatry 11(12): 1126-1138]. Haplotype analysis revealed specific risk as well as protective haplotypes with a minimal P-value of 0.0027. None of the 11 SNPs showed association with BPD. However, analyzing seven BRD1 SNPs obtained from the BPD GWA study, positive associations with BPD was observed with all markers (minimal P-value of 0.0014). The associations reported add further support for the implication of BRD1 with SZ and BPD susceptibility. (c) 2009 Wiley-Liss, Inc.

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Year:  2010        PMID: 19693800     DOI: 10.1002/ajmg.b.31023

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  23 in total

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Journal:  ACS Med Chem Lett       Date:  2014-09-10       Impact factor: 4.345

Review 4.  Biological function and histone recognition of family IV bromodomain-containing proteins.

Authors:  Jonathan T Lloyd; Karen C Glass
Journal:  J Cell Physiol       Date:  2017-06-13       Impact factor: 6.384

5.  Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.

Authors:  David Curtis; Anna E Vine; Andrew McQuillin; Nicholas James Bass; Ana Pereira; Radhika Kandaswamy; Jacob Lawrence; Adebayo Anjorin; Khalid Choudhury; Susmita R Datta; Vinay Puri; Robert Krasucki; Jonathan Pimm; Srinivasa Thirumalai; Digby Quested; Hugh M D Gurling
Journal:  Psychiatr Genet       Date:  2011-02       Impact factor: 2.458

6.  Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia.

Authors:  Mariam M Al Eissa; Sally I Sharp; Niamh L O'Brien; Alessia Fiorentino; Nicholas J Bass; David Curtis; Andrew McQuillin
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2019-03-11       Impact factor: 3.568

Review 7.  HERVs in neuropathogenesis.

Authors:  Tove Christensen
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8.  High-resolution chromosome ideogram representation of recognized genes for bipolar disorder.

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9.  A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families.

Authors:  Lisbeth Venø Kruse; Mette Nyegaard; Ulla Christensen; Steffen Møller-Larsen; Annette Haagerup; Mette Deleuran; Lars Gudmund Hansen; Stine Krogh Venø; Dirk Goossens; Jurgen Del-Favero; Anders Dupont Børglum
Journal:  Eur J Hum Genet       Date:  2012-03-14       Impact factor: 4.246

Review 10.  Genotype-phenotype correlation in Phelan-McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes.

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Journal:  Am J Med Genet A       Date:  2021-05-05       Impact factor: 2.802

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