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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
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.
Pharmacogenetics of inflammatory bowel disease.
Mascheretti S, Croucher PJ, Schreiber S. Mascheretti S, et al. Among authors: schreiber s. Best Pract Res Clin Gastroenterol. 2004 Jun;18(3):597-609. doi: 10.1016/j.bpg.2003.12.001. Best Pract Res Clin Gastroenterol. 2004. PMID: 15157830 Review.
Sarcoidosis is associated with a truncating splice site mutation in BTNL2.
Valentonyte R, Hampe J, Huse K, Rosenstiel P, Albrecht M, Stenzel A, Nagy M, Gaede KI, Franke A, Haesler R, Koch A, Lengauer T, Seegert D, Reiling N, Ehlers S, Schwinger E, Platzer M, Krawczak M, Müller-Quernheim J, Schürmann M, Schreiber S. Valentonyte R, et al. Among authors: schreiber s. Nat Genet. 2005 Apr;37(4):357-64. doi: 10.1038/ng1519. Epub 2005 Feb 27. Nat Genet. 2005. PMID: 15735647
Dissection of the inflammatory bowel disease transcriptome using genome-wide cDNA microarrays.
Costello CM, Mah N, Häsler R, Rosenstiel P, Waetzig GH, Hahn A, Lu T, Gurbuz Y, Nikolaus S, Albrecht M, Hampe J, Lucius R, Klöppel G, Eickhoff H, Lehrach H, Lengauer T, Schreiber S. Costello CM, et al. Among authors: schreiber s. PLoS Med. 2005 Aug;2(8):e199. doi: 10.1371/journal.pmed.0020199. Epub 2005 Aug 23. PLoS Med. 2005. PMID: 16107186 Free PMC article.
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
2,765 results