Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1. (Q48193762)

9 February 2018

title

Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1. (English)

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9 February 2018

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2

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9 February 2018

Douglas Blackwood

1

Douglas H R Blackwood

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9 February 2018

Walter J Muir

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Walter J Muir

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9 February 2018

Pippa A Thomson

3

Pippa A Thomson

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9 February 2018

Kathryn L Evans

4

Kathryn L Evans

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9 February 2018

David J. Porteous

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David J Porteous

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9 February 2018

publication date

1 January 2007

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9 February 2018

published in

Neurotoxicity Research

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9 February 2018

volume

11

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9 February 2018

issue

1

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9 February 2018

page(s)

73-83

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9 February 2018

https://scigraph.springernature.com/pub.10.1007/bf03033484

exact match

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cites work

Auditory P300 and eye tracking dysfunction in schizophrenic pedigrees.

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https://api.crossref.org/works/10.1007%2FBF03033484

Linkage analysis of fifty-seven microsatellite loci to bipolar disorder.

21 January 2018

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Genetic association between schizophrenia and the DISC1 gene in the Scottish population.

21 January 2018

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Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

21 January 2018

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Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence

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

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Polymorphisms within 5' end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population

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A case control and family based association study of the neuregulin1 gene and schizophrenia

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Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus.

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Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory

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Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families

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Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

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Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype.

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The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations

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A follow-up report of a genome search for affective disorder predisposition loci in the Old Order Amish.

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Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes

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Replication of 1q42 linkage in Finnish schizophrenia pedigrees

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Association between genotype at an exonic SNP in DISC1 and normal cognitive aging.

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Association study of polymorphisms in the GluR7, KA1 and KA2 kainate receptor genes (GRIK3, GRIK4, GRIK5) with schizophrenia

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Association study of the DISC1/TRAX locus with schizophrenia in a Japanese population.

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Association study of neuregulin 1 gene with schizophrenia.

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Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q

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DISC1 and neurocognitive function in schizophrenia.

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Bipolar disorder and schizophrenia: convergent molecular data

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A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder

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NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees

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Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families.

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Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia.

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12 December 2020

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

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Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

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Neuregulin 1: genetic support for schizophrenia subtypes

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Genetic linkage and association between chromosome 1q and working memory function in schizophrenia

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Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate

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Support for involvement of neuregulin 1 in schizophrenia pathophysiology

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Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

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Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

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Linkage of familial schizophrenia to chromosome 13q32

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Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia

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Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes

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Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees.

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The dichotomy of schizophrenia and affective disorders in extended pedigrees

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Complex trait analysis of gene expression uncovers polygenic and pleiotropic networks that modulate nervous system function

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A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.

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12 December 2020

Genome-wide scan of homogeneous subtypes of NIMH genetics initiative schizophrenia families.

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A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

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12 December 2020

Linkage of schizophrenia with chromosome 1q loci in Taiwanese families.

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12 December 2020

Do schizophrenia and affective disorder share susceptibility genes?

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12 December 2020

Neuregulin 1 and susceptibility to schizophrenia

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12 December 2020

Cytogenetics and gene discovery in psychiatric disorders.

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12 December 2020

A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42

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12 December 2020

A genome-wide search for schizophrenia susceptibility genes

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12 December 2020

Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder

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12 December 2020

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

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12 December 2020

Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder.

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12 December 2020

Chromosome 1 loci in Finnish schizophrenia families

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12 December 2020

Disruption of two novel genes by a translocation co-segregating with schizophrenia

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12 December 2020

Genomewide Linkage Scan in Schizoaffective Disorder

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12 December 2020

Identifiers

DOI

10.1007/BF03033484

1 reference

9 February 2018

release_alz3bgq5zfbxxn3rvs4yjko5pu

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/alz3bgq5zfbxxn3rvs4yjko5pu

24 November 2022

mapped directly with Wikidata item

PubMed ID

17449450

1 reference

9 February 2018