(Q33396971)

26 July 2017

title

IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production (English)

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26 July 2017

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Neil Walker

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David A. Hafler

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object named as

David A Hafler

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Stephen Sawcer

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John A Todd

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Philip L De Jager

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Jorge R Oksenberg

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26 July 2017

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Stephen L Hauser

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International Multiple Sclerosis Genetics Consortium

26 July 2017

15

object named as

International Multiple Sclerosis Genetics Consortium

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26 July 2017

10

Cristin Aubin

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26 July 2017

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Linda S Wicker

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26 July 2017

4

Kate Downes

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26 July 2017

Lisa M Maier

1

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26 July 2017

Christopher E Lowe

2

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26 July 2017

Jason Cooper

3

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26 July 2017

David E Anderson

5

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26 July 2017

Christopher Severson

6

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Pamela M Clark

7

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26 July 2017

Brian Healy

8

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Alistair Compston

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26 July 2017

publication date

2 January 2009

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26 July 2017

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26 July 2017

volume

5

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26 July 2017

issue

1

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26 July 2017

page(s)

e1000322

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Creative Commons Attribution 4.0 International

26 July 2017

copyright license

start time

2 January 2009

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Protein tyrosine phosphatase PTPN22 in human autoimmunity

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Risk alleles for multiple sclerosis identified by a genomewide study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Both integrated and differential regulation of components of the IL-2/IL-2 receptor system

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Population structure, differential bias and genomic control in a large-scale, case-control association study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Tolerance, not immunity, crucially depends on IL-2.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Haploview: analysis and visualization of LD and haplotype maps

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Immune activation in multiple sclerosis: study of IL-2, sIL-2R, and gamma-IFN levels in serum and cerebrospinal fluid

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.

14 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

IL2RA/CD25 polymorphisms contribute to multiple sclerosis susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

Refining genetic associations in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

PTPN22 Trp620 explains the association of chromosome 1p13 with type 1 diabetes and shows a statistical interaction with HLA class II genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602853

Genomewide Study of Multiple Sclerosis

31 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000322

Serum levels of soluble interleukin-2 receptor alpha (sIL-2Ralpha) as a predictor of outcome in brucellosis

21 January 2018

1 reference

12 December 2020

Toward further mapping of the association between the IL2RA locus and type 1 diabetes

1 reference

12 December 2020

The developing mosaic of autoimmune disease risk

1 reference

12 December 2020

Elevated levels of soluble interleukin-2 receptors in multiple sclerosis

1 reference

12 December 2020

Interleukin-2 receptor levels indicating relapse in multiple sclerosis

1 reference

12 December 2020

Increased soluble interleukin-2 receptor levels in the sera of type 1 diabetic patients

1 reference

12 December 2020

10.1371/JOURNAL.PGEN.1000322

Identifiers

DOI

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26 July 2017

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26 July 2017

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