(Q38367681)

2 September 2017

0 references

Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis (English)

1 reference

2 September 2017

28

1 reference

2 September 2017

P Gourh

2

0 references

Ivan Castellvi

I Castellvi

33

0 references

Antonio Fernandez-Nebro

A Fernandez-Nebro

19

0 references

Norberto Ortego-Centeno

N Ortego-Centeno

6

0 references

Ariane I. Herrick

A Herrick

27

0 references

Javier Martin

J Martin

40

0 references

Gabriela Riemekasten

10

G Riemekasten

1 reference

2 September 2017

14

J D Reveille

1 reference

2 September 2017

32

G Espinosa

1 reference

Miguel Angel Gonzalez-Gay

2 September 2017

23

M A González-Gay

1 reference

2 September 2017

Gracia A Gómez-Anduro

30

I Gómez-Gracia

1 reference

2 September 2017

L M Diaz-Gallo

1

1 reference

2 September 2017

J Broen

3

1 reference

2 September 2017

C Simeon

4

1 reference

2 September 2017

V Fonollosa

5

1 reference

2 September 2017

S Agarwal

7

1 reference

2 September 2017

M C Vonk

8

1 reference

2 September 2017

M Coenen

9

1 reference

2 September 2017

N Hunzelmann

11

1 reference

2 September 2017

R Hesselstrand

12

1 reference

2 September 2017

F K Tan

13

1 reference

2 September 2017

S Assassi

15

1 reference

2 September 2017

F J García-Hernandez

16

1 reference

2 September 2017

P Carreira

17

1 reference

2 September 2017

M T Camps

18

1 reference

2 September 2017

P Garcia de la Peña

20

1 reference

2 September 2017

T Nearney

21

1 reference

2 September 2017

D Hilda

22

1 reference

2 September 2017

P Airo

24

1 reference

2 September 2017

L Beretta

25

1 reference

2 September 2017

R Scorza

26

1 reference

2 September 2017

A Pros

29

1 reference

2 September 2017

L Trapiella

31

1 reference

2 September 2017

T Witte

34

1 reference

2 September 2017

F de Keyser

35

1 reference

2 September 2017

M Vanthuyne

36

1 reference

2 September 2017

M D Mayes

37

1 reference

2 September 2017

T R D J Radstake

38

1 reference

2 September 2017

F C Arnett

39

1 reference

2 September 2017

B Rueda

41

1 reference

2 September 2017

language of work or name

English

0 references

publication date

3 December 2010

1 reference

Annals of the Rheumatic Diseases

2 September 2017

1 reference

2 September 2017

70

1 reference

2 September 2017

3

1 reference

2 September 2017

454-462

1 reference

Interleukin-2 receptor signaling: at the interface between tolerance and immunity

2 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Lymphoid tyrosine phosphatase and autoimmunity: human genetics rediscovers tyrosine phosphatases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Genetic regulation of serum cytokines in systemic lupus erythematosus

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Systemic sclerosis and lupus: points in an interferon-mediated continuum

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Recent advances in the genetics of autoimmune disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

PTPN22 deficiency cooperates with the CD45 E613R allele to break tolerance on a non-autoimmune background.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

How to use an article about genetic association: B: Are the results of the study valid?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Detecting shared pathogenesis from the shared genetics of immune-related diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Relationship of Sjögren's syndrome to other connective tissue and autoimmune disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Genetics and genomic studies in scleroderma (systemic sclerosis).

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Assessing heterogeneity in meta-analysis: Q statistic or I2 index?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Identification of substrates of human protein-tyrosine phosphatase PTPN22

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Measuring inconsistency in meta-analyses

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Assessment of lung involvement.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Role of protein tyrosine phosphatases in T cell activation.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Criteria for the classification of early systemic sclerosis.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Association study designs for complex diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Preliminary criteria for the classification of systemic sclerosis (scleroderma). Subcommittee for scleroderma criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Associated autoimmune diseases in systemic sclerosis define a subset of patients with milder disease: results from 2 large cohorts of European Caucasian patients.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

BANK1 functional variants are associated with susceptibility to diffuse systemic sclerosis in Caucasians

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Association of a functional polymorphism in the IRF5 region with systemic sclerosis in a Japanese population.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotype.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

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

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Lack of association of the PTPN22 gene polymorphism R620W with systemic sclerosis.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

BANK1is a genetic risk factor for diffuse cutaneous systemic sclerosis and has additive effects withIRF5andSTAT4

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

STAT4is a genetic risk factor for systemic sclerosis having additive effects withIRF5on disease susceptibility and related pulmonary fibrosis

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Association between theIRF5rs2004640 functional polymorphism and systemic sclerosis: A new perspective for pulmonary fibrosis

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3170726

Scleroderma (systemic sclerosis): classification, subsets and pathogenesis

3 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21131644

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Geographical variation of disease manifestations in systemic sclerosis: a report from the EULAR Scleroderma Trials and Research (EUSTAR) group database

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21131644

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ARD.2010.130138

1 reference

2 September 2017

1 reference

2 September 2017

1 reference