(Q30437392)

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rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype

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scholarly article

1 reference

Europe PubMed Central

11 November 2017

rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype (English)

1 reference

Europe PubMed Central

11 November 2017

type-1 diabetes

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Patrick Concannon

6

1 reference

Europe PubMed Central

11 November 2017

Constantin Polychronakos

10

1 reference

Europe PubMed Central

11 November 2017

George Eisenbarth

12

object named as

G S Eisenbarth

1 reference

Europe PubMed Central

11 November 2017

7

object named as

C Julier

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Europe PubMed Central

11 November 2017

author name string

A K Steck

1

1 reference

Europe PubMed Central

11 November 2017

E E Baschal

2

1 reference

Europe PubMed Central

11 November 2017

J M Jasinski

3

1 reference

Europe PubMed Central

11 November 2017

B O Boehm

4

1 reference

Europe PubMed Central

11 November 2017

N Bottini

5

1 reference

Europe PubMed Central

11 November 2017

G Morahan

8

1 reference

Europe PubMed Central

11 November 2017

J A Noble

9

1 reference

Europe PubMed Central

11 November 2017

J X She

11

1 reference

Europe PubMed Central

11 November 2017

Type I Diabetes Genetics Consortium

13

1 reference

Europe PubMed Central

11 November 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 December 2009

1 reference

Europe PubMed Central

11 November 2017

Genes and Immunity

1 reference

Europe PubMed Central

11 November 2017

10 Suppl 1

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Europe PubMed Central

11 November 2017

S21-6

1 reference

Europe PubMed Central

11 November 2017

Overview of the Rapid Response data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Reduced CD4+T cell activation in children with type 1 diabetes carrying the PTPN22/Lyp 620Trp variant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Confirmation of the association of the R620W polymorphism in the protein tyrosine phosphatase PTPN22 with type 1 diabetes in a family based study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Genetic association between a lymphoid tyrosine phosphatase (PTPN22) and type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

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=2805459

20 June 2018

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Bfk: a novel weakly proapoptotic member of the Bcl-2 protein family with a BH3 and a BH2 region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Cooperative inhibition of T-cell antigen receptor signaling by a complex between a kinase and a phosphatase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Mapping disease genes: family-based association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2805459

20 June 2018

Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

CD226 Gly307Ser association with multiple autoimmune diseases

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

Lymphoid tyrosine phosphatase (LYP/PTPN22) Arg620Trp variant regulates insulin autoimmunity and progression to type 1 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

A Haplotype-Based Analysis of the PTPN22 Locus in Type 1 Diabetes

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

PTPN22 R620W Functional Variant in Type 1 Diabetes and Autoimmunity Related Traits

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2009.87

21 January 2018

Systematic search for single nucleotide polymorphisms in a lymphoid tyrosine phosphatase gene (PTPN22): association between a promoter polymorphism and type 1 diabetes in Asian populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19956096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the PTPN22/LYP gene with type 1 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19956096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/GENE.2009.87

1 reference

Europe PubMed Central

11 November 2017

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1 reference

Europe PubMed Central

11 November 2017

1 reference

Europe PubMed Central

11 November 2017

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