(Q33688587)

28 July 2017

title

Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk (English)

1 reference

28 July 2017

1 reference

16

Inês Barroso

0 references

Eleanor Wheeler

2

Eleanor Wheeler

0 references

Katherine Fawcett

Katherine A Fawcett

1

0 references

Benjamin Glaser

Benjamin Glaser

11

0 references

Paul W. Franks

Paul W Franks

12

0 references

Mark McCarthy

Mark I McCarthy

13

0 references

Göran Hallmans

5

Göran Hallmans

1 reference

28 July 2017

14

Nicholas J Wareham

1 reference

28 July 2017

Andrew Tym Hattersley

10

Andrew T Hattersley

1 reference

28 July 2017

3

Andrew P Morris

1 reference

28 July 2017

Sally L Ricketts

4

1 reference

28 July 2017

Olov Rolandsson

6

1 reference

28 July 2017

Allan Daly

7

1 reference

28 July 2017

Jon Wasson

8

1 reference

28 July 2017

Alan Permutt

9

1 reference

28 July 2017

Manjinder S Sandhu

15

1 reference

28 July 2017

language of work or name

English

0 references

publication date

22 December 2009

1 reference

28 July 2017

1 reference

28 July 2017

volume

59

1 reference

28 July 2017

issue

3

1 reference

28 July 2017

page(s)

741-746

1 reference

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

28 July 2017

copyright license

start time

27 August 2021

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Common and rare variants in multifactorial susceptibility to common diseases

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Common variants in WFS1 confer risk of type 2 diabetes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

WFS1 protein modulates the free Ca(2+) concentration in the endoplasmic reticulum

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Genome-wide associations of gene expression variation in humans

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Endoplasmic reticulum stress induces Wfs1 gene expression in pancreatic beta-cells via transcriptional activation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Maturity-onset diabetes of the young: from clinical description to molecular genetic characterization

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Power and sample size calculations. A review and computer program

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

The Exeter Family Study of Childhood Health (EFSOCH): study protocol and methodology

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

WFS1 is a novel component of the unfolded protein response and maintains homeostasis of the endoplasmic reticulum in pancreatic beta-cells

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Dietary fat and the risk of clinical type 2 diabetes: the European prospective investigation of Cancer-Norfolk study

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Low faecal elastase 1 concentrations in type 2 diabetes mellitus

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

A quantitative analysis of the relationship between habitual energy expenditure, fitness and the metabolic cardiovascular syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828659

The ADDITION study: proposed trial of the cost-effectiveness of an intensive multifactorial intervention on morbidity and mortality among people with Type 2 diabetes detected by screening

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20028947

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20028947

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association Studies of Genetic Variation in the WFS1 Gene and Type 2 Diabetes in U.K. Populations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20028947

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2337/DB09-0920

1 reference

28 July 2017

1 reference

28 July 2017

1 reference