Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish population (Q47399632)

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29 December 2019

title

Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish population (English)

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29 December 2019

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4

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29 December 2019

Benjamin S Pickard

5

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29 December 2019

David J. Porteous

6

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29 December 2019

Kathryn L Evans

9

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29 December 2019

8

D H R Blackwood

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29 December 2019

7

W J Muir

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29 December 2019

3

S W Morris

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29 December 2019

author name string

P A Thomson

1

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29 December 2019

A Christoforou

2

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29 December 2019

language of work or name

English

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publication date

29 August 2006

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29 December 2019

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29 December 2019

volume

12

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29 December 2019

page(s)

94-104

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29 December 2019

issue

1

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001889

29 December 2019

exact match

0 references

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Multiple novel transcription initiation sites for NRG1

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Untangling the ErbB signalling network

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Aberrant neural and cardiac development in mice lacking the ErbB4 neuregulin receptor

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Heregulin, but not ErbB2 or ErbB3, heterozygous mutant mice exhibit hyperactivity in multiple behavioral tasks

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Neuregulin 1 and susceptibility to schizophrenia

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Neuregulin-1 immunoglobulin-like domain mutant mice: clozapine sensitivity and impaired latent inhibition

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Regulation of NMDA receptors by neuregulin signaling in prefrontal cortex.

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Integrative proteomics: functional and molecular characterization of a particular glutamate-related neuregulin isoform

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Neuregulin1 downregulates postsynaptic GABAA receptors at the hippocampal inhibitory synapse

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Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

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A genome-wide search for schizophrenia susceptibility genes

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Linkage of familial schizophrenia to chromosome 13q32

21 January 2018

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

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

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

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Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

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

21 January 2018

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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.

21 January 2018

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No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).

21 January 2018

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Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia.

21 January 2018

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Association study of neuregulin 1 gene with schizophrenia.

21 January 2018

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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.

21 January 2018

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

21 January 2018

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A diagnostic interview: the schedule for affective disorders and schizophrenia

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Haploview: analysis and visualization of LD and haplotype maps

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Pedigree disequilibrium tests for multilocus haplotypes.

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A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

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Expression analysis of neuregulin-1 in the dorsolateral prefrontal cortex in schizophrenia

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Evidence for shared susceptibility in bipolar disorder and schizophrenia

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

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Support for involvement of neuregulin 1 in schizophrenia pathophysiology

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7 January 2021

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

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7 January 2021

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

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Case-control and family-based association studies between the neuregulin 1 (Arg38Gln) polymorphism and schizophrenia

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No association with the neuregulin 1 haplotype to Japanese schizophrenia

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7 January 2021

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Neuregulin genotype and medication response in Finnish patients with schizophrenia

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Identifiers

DOI

10.1038/SJ.MP.4001889

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940976%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 December 2019

0 references

1 reference