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Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p.
Hampe J, Frenzel H, Mirza MM, Croucher PJ, Cuthbert A, Mascheretti S, Huse K, Platzer M, Bridger S, Meyer B, Nürnberg P, Stokkers P, Krawczak M, Mathew CG, Curran M, Schreiber S. Hampe J, et al. Among authors: schreiber s. Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):321-6. doi: 10.1073/pnas.261567999. Epub 2001 Dec 18. Proc Natl Acad Sci U S A. 2002. PMID: 11752413 Free PMC article.
Response to infliximab treatment in Crohn's disease is not associated with mutations in the CARD15 (NOD2) gene: an analysis in 534 patients from two multicenter, prospective GCP-level trials.
Mascheretti S, Hampe J, Croucher PJ, Nikolaus S, Andus T, Schubert S, Olson A, Bao W, Fölsch UR, Schreiber S. Mascheretti S, et al. Among authors: schreiber s. Pharmacogenetics. 2002 Oct;12(7):509-15. doi: 10.1097/00008571-200210000-00002. Pharmacogenetics. 2002. PMID: 12360101 Clinical Trial.
Genetic variation in DLG5 is associated with inflammatory bowel disease.
Stoll M, Corneliussen B, Costello CM, Waetzig GH, Mellgard B, Koch WA, Rosenstiel P, Albrecht M, Croucher PJ, Seegert D, Nikolaus S, Hampe J, Lengauer T, Pierrou S, Foelsch UR, Mathew CG, Lagerstrom-Fermer M, Schreiber S. Stoll M, et al. Among authors: schreiber s. Nat Genet. 2004 May;36(5):476-80. doi: 10.1038/ng1345. Epub 2004 Apr 11. Nat Genet. 2004. PMID: 15107852
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Hampe J, Franke A, Rosenstiel P, Till A, Teuber M, Huse K, Albrecht M, Mayr G, De La Vega FM, Briggs J, Günther S, Prescott NJ, Onnie CM, Häsler R, Sipos B, Fölsch UR, Lengauer T, Platzer M, Mathew CG, Krawczak M, Schreiber S. Hampe J, et al. Among authors: schreiber s. Nat Genet. 2007 Feb;39(2):207-11. doi: 10.1038/ng1954. Epub 2006 Dec 31. Nat Genet. 2007. PMID: 17200669
2,743 results