Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. (Q53621277)

16 May 2018

title

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. (English)

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16 May 2018

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7

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Nicholas Bray

object named as

Nicholas J Bray

1

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author name string

Anna Preece

2

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Nigel M Williams

3

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Valentina Moskvina

4

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Paul R Buckland

5

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Michael J Owen

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publication date

25 May 2005

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16 May 2018

published in

Human Molecular Genetics

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volume

14

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issue

14

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page(s)

1947-1954

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16 May 2018

Heritability estimates for psychotic disorders: the Maudsley twin psychosis series

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Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

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The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease

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Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

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Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).

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Association of the DTNBP1 locus with schizophrenia in a U.S. population

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Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia

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Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia

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Human dysbindin (DTNBP1) gene expression in normal brain and in schizophrenic prefrontal cortex and midbrain

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Parental imprinting studied by allele-specific primer extension after PCR: paternal X chromosome-linked genes are transcribed prior to preferential paternal X chromosome inactivation

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Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families

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Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain

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Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

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Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

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Model-free analysis and permutation tests for allelic associations.

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDI199

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16 May 2018

PubMed ID

15917270

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16 May 2018