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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Philippe Dieudé

Paris Diderot University

AP-HP

INSERM U699

and Hôpital Bichat Claude Bernard

France

[email]@bch.aphp.fr

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Paris Diderot University, AP-HP, INSERM U699, and Hôpital Bichat Claude Bernard, France. 2007 - 2011
  • LREPR-EA3886, Evry-Génopole, université d'Evry-Val-d'Essonne, France. 2009
  • Université Paris 7, Paris, France. 2008

References

  1. Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: Association with the functional IRAK1 196Phe/532Ser haplotype. Dieudé, P., Bouaziz, M., Guedj, M., Riemekasten, G., Airò, P., Müller, M., Cusi, D., Matucci-Cerinic, M., Melchers, I., Koenig, W., Salvi, E., Wichmann, H.E., Cuomo, G., Hachulla, E., Diot, E., Hunzelmann, N., Caramaschi, P., Mouthon, L., Riccieri, V., Distler, J., Tarner, I., Avouac, J., Meyer, O., Kahan, A., Chiocchia, G., Boileau, C., Allanore, Y. Arthritis Rheum. (2011) [Pubmed]
  2. NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesis. Dieudé, P., Guedj, M., Wipff, J., Ruiz, B., Riemekasten, G., Airo, P., Melchers, I., Hachulla, E., Cerinic, M.M., Diot, E., Hunzelmann, N., Caramaschi, P., Sibilia, J., Tiev, K., Mouthon, L., Riccieri, V., Cracowski, J.L., Carpentier, P.H., Distler, J., Amoura, Z., Tarner, I., Avouac, J., Meyer, O., Kahan, A., Boileau, C., Allanore, Y. Ann. Rheum. Dis. (2011) [Pubmed]
  3. Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis. Dieudé, P., Guedj, M., Truchetet, M.E., Wipff, J., Revillod, L., Riemekasten, G., Matucci-Cerinic, M., Melchers, I., Hachulla, E., Airo, P., Diot, E., Hunzelmann, N., Mouthon, L., Cabane, J., Cracowski, J.L., Riccieri, V., Distler, J., Amoura, Z., Valentini, G., Camaraschi, P., Tarner, I., Frances, C., Carpentier, P., Brembilla, N.C., Meyer, O., Kahan, A., Chizzolini, C., Boileau, C., Allanore, Y. Arthritis Rheum. (2011) [Pubmed]
  4. High Levels of Anti-Cyclic Citrullinated Peptide Autoantibodies Are Associated with Co-occurrence of Pulmonary Diseases with Rheumatoid Arthritis. Aubart, F., Crestani, B., Nicaise-Roland, P., Tubach, F., Bollet, C., Dawidowicz, K., Quintin, E., Hayem, G., Palazzo, E., Meyer, O., Chollet-Martin, S., Dieudé, P. J. Rheumatol. (2011) [Pubmed]
  5. Phenotype-haplotype correlation of IRF5 in systemic sclerosis: role of 2 haplotypes in disease severity. Dieude, P., Dawidowicz, K., Guedj, M., Legrain, Y., Wipff, J., Hachulla, E., Diot, E., Sibilia, J., Mouthon, L., Cabane, J., Amoura, Z., Crakowski, J.L., Carpentier, P., Avouac, J., Meyer, O., Kahan, A., Boileau, C., Allanore, Y. J. Rheumatol. (2010) [Pubmed]
  6. Association between the IRF5 rs2004640 functional polymorphism and systemic sclerosis: a new perspective for pulmonary fibrosis. Dieudé, P., Guedj, M., Wipff, J., Avouac, J., Fajardy, I., Diot, E., Granel, B., Sibilia, J., Cabane, J., Mouthon, L., Cracowski, J.L., Carpentier, P.H., Hachulla, E., Meyer, O., Kahan, A., Boileau, C., Allanore, Y. Arthritis Rheum. (2009) [Pubmed]
  7. STAT4 is a genetic risk factor for systemic sclerosis having additive effects with IRF5 on disease susceptibility and related pulmonary fibrosis. Dieudé, P., Guedj, M., Wipff, J., Ruiz, B., Hachulla, E., Diot, E., Granel, B., Sibilia, J., Tiev, K., Mouthon, L., Cracowski, J.L., Carpentier, P.H., Amoura, Z., Fajardy, I., Avouac, J., Meyer, O., Kahan, A., Boileau, C., Allanore, Y. Arthritis Rheum. (2009) [Pubmed]
  8. Rheumatic diseases: environment and genetics. Dieudé, P. Joint. Bone. Spine (2009) [Pubmed]
  9. The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis. Dieudé, P., Guedj, M., Wipff, J., Avouac, J., Hachulla, E., Diot, E., Granel, B., Sibilia, J., Cabane, J., Meyer, O., Mouthon, L., Kahan, A., Boileau, C., Allanore, Y. Arthritis Rheum. (2008) [Pubmed]
  10. The TNFRSF1A R92Q mutation is frequent in rheumatoid arthritis but shows no evidence for association or linkage with the disease. Dieudé, P., Goossens, M., Cornélis, F., Michou, L., Bardin, T., Tchernitchko, D.O. Ann. Rheum. Dis. (2007) [Pubmed]
 
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