O. Meyer

发表

Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population

J. Cracowski, P. Dieudé, C. Boileau, 2010, Annals of the rheumatic diseases.

High N-terminal pro-brain natriuretic peptide levels and low diffusing capacity for carbon monoxide as independent predictors of the occurrence of precapillary pulmonary arterial hypertension in patients with systemic sclerosis.

D. Borderie, O. Ekindjian, L. Mouthon, 2008, Arthritis and rheumatism.

Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis

Erika Salvi, Mohamad Saad, Eric Hachulla, 2011, PLoS genetics.

STAT4 is a genetic risk factor for systemic sclerosis having additive effects with IRF5 on disease susceptibility and related pulmonary fibrosis.

I. Fajardy, J. Cracowski, P. Dieudé, 2009, Arthritis and rheumatism.

Association between the IRF5 rs2004640 functional polymorphism and systemic sclerosis: a new perspective for pulmonary fibrosis.

I. Fajardy, J. Cracowski, P. Dieudé, 2009, Arthritis and rheumatism.

Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis.

J. Cracowski, P. Dieudé, C. Boileau, 2011, Arthritis and rheumatism.

Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension.

C. Junien, C. Boileau, L. Mouthon, 2006, Rheumatology.

Association of hypoxia‐inducible factor 1A (HIF1A) gene polymorphisms with systemic sclerosis in a French European Caucasian population

P. Dieudé, C. Boileau, L. Mouthon, 2009, Scandinavian journal of rheumatology.

Association of a KCNA5 gene polymorphism with systemic sclerosis-associated pulmonary arterial hypertension in the European Caucasian population.

M. Humbert, J. Cracowski, P. Dieudé, 2010, Arthritis and rheumatism.

Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: association with the functional IRAK1 196Phe/532Ser haplotype.

H. Wichmann, W. Koenig, P. Dieudé, 2011, Arthritis and rheumatism.

BANK1 is a genetic risk factor for diffuse cutaneous systemic sclerosis and has additive effects with IRF5 and STAT4.

J. Cracowski, P. Dieudé, C. Boileau, 2009, Arthritis and rheumatism.

Validation of French version of the Scleroderma Health Assessment Questionnaire (SSc HAQ)

O. Chassany, L. Mouthon, J. Cabane, 2005, Clinical Rheumatology.

NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesis

J. Cracowski, P. Dieudé, C. Boileau, 2010, Annals of the rheumatic diseases.

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

P. Dieudé, C. Boileau, L. Mouthon, 2008, Arthritis and rheumatism.

Treatment patterns in adults with immune thrombocytopenia before, during and after use of thrombopoietin receptor agonists: a longitudinal prescription database study from Germany

H. Richter, O. Meyer, A. Lebioda, 2021, Hematology.

Vaccination in adults with auto-immune disease and/or drug related immune deficiency: results of the GEVACCIM Delphi survey.

J. Pouchot, X. Mariette, E. Hachulla, 2009, Vaccine.

Impact of pain in health related quality of life of patients with systemic sclerosis.

O. Chassany, J. Pouchot, L. Mouthon, 2006, Rheumatology.

[Quality of life assessment with the MOS-SF36 in patients with systemic sclerosis].

O. Chassany, L. Mouthon, D. Farge, 2004, La Revue de medecine interne.

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

P. Dieudé, C. Boileau, L. Mouthon, 2006, Annals of the rheumatic diseases.