A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia (Q24683040)

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English	A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia	scientific article

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A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia (English)

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Andrew McQuillin

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Andrew McQuillin

2

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David Curtis

16

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17

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David St Clair

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author name string

Khalid Choudhury

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Vinay Puri

3

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Jonathan Pimm

4

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Susmita Datta

5

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Srinivasa Thirumalai

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Robert Krasucki

7

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Jacob Lawrence

8

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Nicholas J Bass

9

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Digby Quested

10

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Caroline Crombie

11

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Gillian Fraser

12

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Nicholas Walker

13

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Haitham Nadeem

14

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Sophie Johnson

15

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Hugh M D Gurling

18

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language of work or name

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publication date

April 2007

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American Journal of Human Genetics

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80

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4

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664-72

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Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

FXYD7 is a brain-specific regulator of Na,K-ATPase alpha 1-beta isozymes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

Primer3 on the WWW for general users and for biologist programmers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

Efficiency and power in genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

FXYD3 (Mat-8), a new regulator of Na,K-ATPase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

The FXYD gene family of small ion transport regulators or channels: cDNA sequence, protein signature sequence, and expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

7 April 2017

Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

Role of FXYD proteins in ion transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

FXYD proteins: new regulators of Na-K-ATPase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British sample

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

Phosphohippolin expression in the rat central nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

FXYD proteins: new tissue-specific regulators of the ubiquitous Na,K-ATPase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

Phospholemman (FXYD1) associates with Na,K-ATPase and regulates its transport properties

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

Molecular cloning and characterization of a novel phospholemman-like protein from rat hippocampus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

Symptoms, signs, and diagnosis of schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 September 2017

Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS4).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 November 2018

GENECOUNTING: haplotype analysis with missing genotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 November 2018

Model-free analysis and permutation tests for allelic associations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1852702

28 November 2018

Linkage study of schizophrenia with markers on chromosome 11 in two Japanese pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/17357072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/17357072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage results on 11Q21-22 in Eastern Quebec pedigrees densely affected by schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17357072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Program Report: GENECOUNTING Support Programs

1 reference

https://pubmed.ncbi.nlm.nih.gov/17357072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A quick and simple method for detecting subjects with abnormal genetic background in case-control samples

1 reference

https://pubmed.ncbi.nlm.nih.gov/17357072

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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