scholarly article | Q13442814 |
meta-analysis | Q815382 |
P819 | ADS bibcode | 2011PLoSO...624292T |
P356 | DOI | 10.1371/JOURNAL.PONE.0024292 |
P932 | PMC publication ID | 3174938 |
P698 | PubMed publication ID | 21949702 |
P5875 | ResearchGate publication ID | 51665627 |
P50 | author | Gianfranco Ferraccioli | Q41067658 |
Valerio Napolioni | Q43235166 | ||
Elisa Gremese | Q50166371 | ||
Alice Mannocci | Q55543098 | ||
Barbara Tolusso | Q56444226 | ||
Stefano Alivernini | Q57080600 | ||
Silvia Canestri | Q58328493 | ||
Silvia Laura Bosello | Q114314203 | ||
Michele Ciro Totaro | Q114314215 | ||
P2093 | author name string | Francesca Faustini | |
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Rheumatoid arthritis seropositive for the rheumatoid factor is linked to the protein tyrosine phosphatase nonreceptor 22-620W allele | Q24812738 | ||
The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritis | Q27860872 | ||
Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population | Q28248685 | ||
A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes | Q28248848 | ||
Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant | Q28280659 | ||
Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus | Q28301821 | ||
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 | Q28301839 | ||
Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins | Q31460983 | ||
Investigation of potential non-HLA rheumatoid arthritis susceptibility loci in a European cohort increases the evidence for nine markers | Q34125266 | ||
PTPN22 polymorphism and anti-cyclic citrullinated peptide antibodies in combination strongly predicts future onset of rheumatoid arthritis and has a specificity of 100% for the disease | Q34896568 | ||
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 | Q34897145 | ||
Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study | Q36171863 | ||
The PTPN22 1858C/T polymorphism is associated with anti-cyclic citrullinated peptide antibody-positive early rheumatoid arthritis in northern Sweden | Q36392280 | ||
PTPN22: setting thresholds for autoimmunity | Q36491114 | ||
Association of common polymorphisms in known susceptibility genes with rheumatoid arthritis in a Slovak population using osteoarthritis patients as controls | Q37270770 | ||
Rheumatoid arthritis: a view of the current genetic landscape | Q37315484 | ||
Ethnogenetic heterogeneity of rheumatoid arthritis-implications for pathogenesis | Q37710382 | ||
The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population | Q38936485 | ||
Functional polymorphisms of PTPN22 and FcgR genes in Tunisian patients with rheumatoid arthritis. | Q39448372 | ||
Reevaluation of the interaction between HLA-DRB1 shared epitope alleles, PTPN22, and smoking in determining susceptibility to autoantibody-positive and autoantibody-negative rheumatoid arthritis in a large UK Caucasian population | Q42632057 | ||
Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients. | Q42680902 | ||
PTPN22 1858C>T polymorphism is strongly associated with rheumatoid arthritis but not with a response to methotrexate therapy | Q42871416 | ||
Discovery of a novel submicromolar inhibitor of the lymphoid specific tyrosine phosphatase. | Q43106114 | ||
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 | Q44449408 | ||
Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes | Q44932416 | ||
Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects | Q45129416 | ||
No association of PTPN22 gene polymorphism with rheumatoid arthritis in Turkey | Q46055652 | ||
Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases | Q46368513 | ||
The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis. | Q46521556 | ||
Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: further support that PTPN22 is an autoimmunity gene | Q46525978 | ||
Association of the PTPN22 C1858T single-nucleotide polymorphism with rheumatoid arthritis phenotypes in an inception cohort. | Q46689842 | ||
Auto-antibodies, HLA and PTPN22: susceptibility markers for rheumatoid arthritis | Q46835340 | ||
Association between protein tyrosine phosphatase 22 variant R620W in conjunction with the HLA-DRB1 shared epitope and humoral autoimmunity to an immunodominant epitope of cartilage-specific type II collagen in early rheumatoid arthritis | Q46872978 | ||
Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis | Q54330502 | ||
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The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples | Q57154867 | ||
The 620W allele is the PTPN22 genetic variant conferring susceptibility to RA in a Dutch population | Q58234945 | ||
Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma | Q59697424 | ||
The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases | Q80161055 | ||
The PTPN22 promoter polymorphism -1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material | Q80697518 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | rheumatoid arthritis | Q187255 |
meta-analysis | Q815382 | ||
P304 | page(s) | e24292 | |
P577 | publication date | 2011-09-16 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | PTPN22 1858C>T polymorphism distribution in Europe and association with rheumatoid arthritis: case-control study and meta-analysis | |
P478 | volume | 6 |
Q34447782 | Assessment of protein tyrosine phosphatases number 22 polymorphism prevalence among rheumatoid arthritis patients: A study on Iranian patients |
Q36335826 | Association between PTPN22 C1858T polymorphism and alopecia areata risk |
Q46840442 | Association of PTPN22 1858C→T polymorphism, HLA-DRB1 shared epitope and autoantibodies with rheumatoid arthritis. |
Q43654959 | Association of PTPN22 rs2476601 and EGFR rs17337023 Gene polymorphisms and rheumatoid arthritis in Zahedan, Southeast Iran. |
Q51046617 | Association of STAT4 rs7574865 and PTPN22 rs2476601 polymorphisms with rheumatoid arthritis and non-systemically reacting antibodies in Egyptian patients. |
Q28482717 | Biochemical and functional studies of lymphoid-specific tyrosine phosphatase (Lyp) variants S201F and R266W |
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Q90207982 | The Contribution of PTPN22 to Rheumatic Disease |
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Q43646920 | The impact of CTLA4 and PTPN22 genes polymorphisms on long-term renal allograft function and transplant outcomes |
Q37054990 | The role of PTPN22 C1858T gene polymorphism in diabetes mellitus type 1: first evaluation in Greek children and adolescents |
Q44532167 | Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population |
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