Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue (Q33403872)

26 July 2017

0 references

Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue (English)

1 reference

26 July 2017

1 reference

2

S Ibrahim

1 reference

26 July 2017

J Zheng

1

1 reference

26 July 2017

F Petersen

series ordinal

3

1 reference

26 July 2017

X Yu

series ordinal

4

1 reference

26 July 2017

18 October 2012

1 reference

26 July 2017

1 reference

26 July 2017

13

1 reference

26 July 2017

641-652

1 reference

26 July 2017

8

1 reference

https://scigraph.springernature.com/pub.10.1038/gene.2012.46

26 July 2017

0 references

cites work

Defining the role of the MHC in autoimmunity: a review and pooled analysis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Cutting edge: the PTPN22 allelic variant associated with autoimmunity impairs B cell signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22 gene regulates natural killer cell proliferation during in vitro expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PEST domain-enriched tyrosine phosphatase (PEP) regulation of effector/memory T cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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/10.1038%2FGENE.2012.46

The functional genetic variation in the PTPN22 gene has a negligible effect on the susceptibility to develop inflammatory bowel disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Protein tyrosine phosphatase non-receptor type 22 gene variants at position 1858 are associated with type 1 and type 2 diabetes in Estonian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22/LYP 1858C>T gene polymorphism and susceptibility to endometriosis in a Polish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22 1858C/T polymorphism is associated with anti-cyclic citrullinated peptide antibody-positive early rheumatoid arthritis in northern Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22 R620W promotes production of anti-AChR autoantibodies and IL-2 in myasthenia gravis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of PTPN22 1858 single-nucleotide polymorphism with rheumatoid arthritis in a German cohort: higher frequency of the risk allele in male compared to female patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

A case-control study of tyrosine phosphatase (PTPN22) confirms the lack of association with Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of common polymorphisms in known susceptibility genes with rheumatoid arthritis in a Slovak population using osteoarthritis patients as controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Sex-specific association of the human PTPN22 1858T-allele with type 1 diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Investigation of genetic variation across the protein tyrosine phosphatase gene in patients with rheumatoid arthritis in the UK.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The non-synonymous C1858T substitution in the PTPN22 gene is associated with susceptibility to the severe forms of alopecia areata.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Shared and distinct genetic variants in type 1 diabetes and celiac disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of R602W in a protein tyrosine phosphatase gene with a high risk of rheumatoid arthritis in a British population: evidence for an early onset/disease severity effect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of the PTPN22 C1858T single-nucleotide polymorphism with rheumatoid arthritis phenotypes in an inception cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The functional R620W variant of the PTPN22 gene is associated with celiac disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22-1858C>T (R620W) functional polymorphism is associated with generalized vitiligo in the Romanian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The protein tyrosine phosphatase nonreceptor 22 (PTPN22) is associated with high GAD antibody titer in latent autoimmune diabetes in adults: Non Insulin Requiring Autoimmune Diabetes (NIRAD) Study 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of the PTPN22 R620W polymorphism with increased risk for SLE in the genetically homogeneous population of Crete

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of functional variants of PTPN22 and tp53 in psoriatic arthritis: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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/10.1038%2FGENE.2012.46

PTPN22 C1858T polymorphism in women with endometriosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of the PTPN22 R620W polymorphism with anti-topoisomerase I- and anticentromere antibody-positive systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association between type 1 diabetes and GWAS SNPs in the southeast US Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22 1858T is not a risk factor for North American pemphigus vulgaris

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Clinical characteristics and PTPN22 1858C/T variant analysis in Jordanian Arab vitiligo patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The role of PTPN22 gene polymorphism in childhood immune thrombocytopenic purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

No association of PTPN22 gene polymorphism with rheumatoid arthritis in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Lymphoid tyrosine phosphatase R620W variant and inflammatory bowel disease in Tunisia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22 R620W polymorphism is not associated with systemic rheumatic diseases in South Africans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Haplotype analysis revealed no association between the PTPN22 gene and RA in a Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Prevalence of common disease-associated variants in Asian Indians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22 allele polymorphisms in 15 Chinese populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Recent advances in the genetics of autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of PTPN22 1858C/T polymorphism with vitiligo susceptibility in Gujarat population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The protein tyrosine phosphatase non-receptor type 22 C1858T polymorphism is a joint susceptibility locus for immunthyroiditis and autoimmune diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Genetic risk markers related to diabetes-associated autoantibodies in young patients with type 1 diabetes in berlin, Germany

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of PTPN22 C1858T and CTLA-4 A49G polymorphisms with Type 1 Diabetes in Croatians

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The association between the PTPN22 1858C>T variant and type 1 diabetes depends on HLA risk and GAD65 autoantibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Common and different genetic background for rheumatoid arthritis and coeliac disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Testing for linkage and association with rheumatoid arthritis a ptpn22 promoter polymorphism reported to be associated and linked with type 1 diabetes in the Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: further support that PTPN22 is an autoimmunity gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22 R620W polymorphism associates with RF positive rheumatoid arthritis in a dose-dependent manner but not with HLA-SE status

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

PTPN22 1858C>T polymorphism is strongly associated with rheumatoid arthritis but not with a response to methotrexate therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Evaluation of the rheumatoid arthritis susceptibility loci HLA-DRB1, PTPN22, OLIG3/TNFAIP3, STAT4 and TRAF1/C5 in an inception cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of the PTPN22 locus with rheumatoid arthritis in a New Zealand Caucasian cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

No association of PTPN22 R620W gene polymorphism with rheumatic heart disease and systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Evaluation of the genetic association of thePTPN22 R620W polymorphism in familial and sporadic systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22 620W allele is a risk factor for Wegener's granulomatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Overlap of disease susceptibility loci for rheumatoid arthritis and juvenile idiopathic arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22gain-of-function+1858T(+) genotypes correlate with low IL-2 expression in thymomas and predispose to myasthenia gravis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The autoimmunity-related polymorphism PTPN22 1858C/T is associated with anti-titin antibody-positive myasthenia gravis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Polymorphisms in the PTPN22 region are associated with psoriasis of early onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Genome-wide association analysis identifies three psoriasis susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association between the PTPN22 +1858 C/T polymorphism and psoriatic arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Genome-wide association study in alopecia areata implicates both innate and adaptive immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The protein tyrosine phosphatase N22 gene is associated with juvenile and adult idiopathic inflammatory myopathy independent of the HLA 8.1 haplotype in British Caucasian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Increased representation of the PTPN22 mutation in patients with immune thrombocytopenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Lack of association between ankylosing spondylitis and a functional polymorphism of PTPN22 proposed as a general susceptibility marker for autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Primary sclerosing cholangitis: diagnosis and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Pemphigus vulgaris and its active disease mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Protein tyrosine phosphatase PTPN22 in human autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

High frequency of autoreactive myelin proteolipid protein-specific T cells in the periphery of naive mice: mechanisms of selection of the self-reactive repertoire

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Multiple sclerosis candidate autoantigens except myelin oligodendrocyte glycoprotein are transcribed in human thymus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

The 620W allele is the PTPN22 genetic variant conferring susceptibility to RA in a Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Perifollicular and Perivascular Mouse Skin Mast Cells Express Corticotropin-Releasing Hormone Receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

Finnish case-control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

The PTPN22 promoter polymorphism -1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Evaluating the role of the genetic variations of PTPN22, NFKB1, and FcGRIIIA genes in inflammatory bowel disease: A meta-analysis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Atherosclerosis and PTPN22: a study in coronary artery disease

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Association of the PTPN22/LYP gene with type 1 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Association analysis of the PTPN22 gene in childhood-onset systemic lupus erythematosus in Mexican population

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Association of the PTPN22 gene polymorphism with autoantibody positivity in Turkish rheumatoid arthritis patients

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

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://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

The R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

The PTPN22 1858T variant is not associated with primary biliary cirrhosis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

PTPN22 R620W polymorphism is not associated with pemphigus

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.46

7 January 2021

Identifiers

DOI

10.1038/GENE.2012.46

1 reference

Dimensions Publication ID

26 July 2017

0 references

1 reference