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Page 1
CARD15 mutations in Blau syndrome.
Miceli-Richard C, Lesage S, Rybojad M, Prieur AM, Manouvrier-Hanu S, Häfner R, Chamaillard M, Zouali H, Thomas G, Hugot JP. Miceli-Richard C, et al. Among authors: thomas g. Nat Genet. 2001 Sep;29(1):19-20. doi: 10.1038/ng720. Nat Genet. 2001. PMID: 11528384
CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.
Lesage S, Zouali H, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Binder V, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, Merlin F, Chamaillard M, Jannot AS, Thomas G, Hugot JP; EPWG-IBD Group; EPIMAD Group; GETAID Group. Lesage S, et al. Among authors: thomas g. Am J Hum Genet. 2002 Apr;70(4):845-57. doi: 10.1086/339432. Epub 2002 Mar 1. Am J Hum Genet. 2002. PMID: 11875755 Free PMC article.
CARD15/NOD2 analyses in spondylarthropathy.
Miceli-Richard C, Zouali H, Lesage S, Thomas G, Hugot JP, Said-Nahal R, Breban M. Miceli-Richard C, et al. Among authors: thomas g. Arthritis Rheum. 2002 May;46(5):1405-6. doi: 10.1002/art.10196. Arthritis Rheum. 2002. PMID: 12115249 Free article. No abstract available.
Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases.
Chamaillard M, Philpott D, Girardin SE, Zouali H, Lesage S, Chareyre F, Bui TH, Giovannini M, Zaehringer U, Penard-Lacronique V, Sansonetti PJ, Hugot JP, Thomas G. Chamaillard M, et al. Among authors: thomas g. Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3455-60. doi: 10.1073/pnas.0530276100. Epub 2003 Mar 7. Proc Natl Acad Sci U S A. 2003. PMID: 12626759 Free PMC article.
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cézard JP, Belaiche J, Almer S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, Gower-Rousseau C, Macry J, Colombel JF, Sahbatou M, Thomas G. Hugot JP, et al. Among authors: thomas g. Nature. 2001 May 31;411(6837):599-603. doi: 10.1038/35079107. Nature. 2001. PMID: 11385576
Clustering of Crohn's disease within affected sibships.
Hugot JP, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, Montague S, Gassull M, Christensen S, Finkel Y, Gower-Rousseau C, Modigliani R, Zouali H, Lesage S, Chamaillard M, Macry J, Thomas G, Victor JM; GETAID. Hugot JP, et al. Among authors: thomas g. Eur J Hum Genet. 2003 Feb;11(2):179-84. doi: 10.1038/sj.ejhg.5200932. Eur J Hum Genet. 2003. PMID: 12634866
Significant linkage to spondyloarthropathy on 9q31-34.
Miceli-Richard C, Zouali H, Said-Nahal R, Lesage S, Merlin F, De Toma C, Blanche H, Sahbatou M, Dougados M, Thomas G, Breban M, Hugot JP; Groupe Français d'Etude Génétique des Spondylarthropathies. Miceli-Richard C, et al. Among authors: thomas g. Hum Mol Genet. 2004 Aug 1;13(15):1641-8. doi: 10.1093/hmg/ddh179. Hum Mol Genet. 2004. PMID: 15234954
Etiology of the inflammatory bowel diseases.
Hugot JP, Zouali H, Lesage S, Thomas G. Hugot JP, et al. Among authors: thomas g. Int J Colorectal Dis. 1999 Feb;14(1):2-9. doi: 10.1007/s003840050175. Int J Colorectal Dis. 1999. PMID: 10207723 Review.
Genetic analyses of chromosome 12 loci in Crohn's disease.
Lesage S, Zouali H, Colombel JF, Belaiche J, Cézard JP, Tysk C, Almer S, Gassull M, Binder V, Chamaillard M, Le Gall I, Thomas G, Hugot JP. Lesage S, et al. Among authors: thomas g. Gut. 2000 Dec;47(6):787-91. doi: 10.1136/gut.47.6.787. Gut. 2000. PMID: 11076876 Free PMC article.
6,034 results