Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations (Q57403348)

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4 January 2020

title

Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations (English)

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4 January 2020

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4 January 2020

Zhang F

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4 January 2020

Liu X

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4 January 2020

Sun X

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Sham PC

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4 January 2020

Crombie C

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4 January 2020

Ma X

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4 January 2020

Wang Q

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4 January 2020

Meng H

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4 January 2020

Deng W

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4 January 2020

Yates P

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4 January 2020

Hu X

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4 January 2020

Walker N

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St Clair D

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4 January 2020

Collier DA

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language of work or name

English

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publication date

1 November 2005

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4 January 2020

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volume

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issue

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4 January 2020

page(s)

1037-1044

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Linkage and associated studies of schizophrenia

4 January 2020

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

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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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Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families

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

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

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No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study

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Linkage disequlibrium in the DTNBP1 (dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in Israel: findings from identity by descent haplotype sharing analysis

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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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Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

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Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

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