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Genetics of Crohn disease, an archetypal inflammatory barrier disease.
Schreiber S, Rosenstiel P, Albrecht M, Hampe J, Krawczak M. Schreiber S, et al. Nat Rev Genet. 2005 May;6(5):376-88. doi: 10.1038/nrg1607. Nat Rev Genet. 2005. PMID: 15861209 Review.
Tumour necrosis factor alpha and interleukin 1beta in relapse of Crohn's disease.
Schreiber S, Nikolaus S, Hampe J, Hämling J, Koop I, Groessner B, Lochs H, Raedler A. Schreiber S, et al. Lancet. 1999 Feb 6;353(9151):459-61. doi: 10.1016/S0140-6736(98)03339-X. Lancet. 1999. PMID: 9989717
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort.
Hampe J, Schreiber S, Shaw SH, Lau KF, Bridger S, Macpherson AJ, Cardon LR, Sakul H, Harris TJ, Buckler A, Hall J, Stokkers P, van Deventer SJ, Nürnberg P, Mirza MM, Lee JC, Lennard-Jones JE, Mathew CG, Curran ME. Hampe J, et al. Am J Hum Genet. 1999 Mar;64(3):808-16. doi: 10.1086/302294. Am J Hum Genet. 1999. PMID: 10053016 Free PMC article.
Linkage of inflammatory bowel disease to human chromosome 6p.
Hampe J, Shaw SH, Saiz R, Leysens N, Lantermann A, Mascheretti S, Lynch NJ, MacPherson AJ, Bridger S, van Deventer S, Stokkers P, Morin P, Mirza MM, Forbes A, Lennard-Jones JE, Mathew CG, Curran ME, Schreiber S. Hampe J, et al. Am J Hum Genet. 1999 Dec;65(6):1647-55. doi: 10.1086/302677. Am J Hum Genet. 1999. PMID: 10577918 Free PMC article.
Anticipation in inflammatory bowel disease: a phenomenon caused by an accumulation of confounders.
Hampe J, Heymann K, Kruis W, Raedler A, Fölsch UR, Schreiber S. Hampe J, et al. Am J Med Genet. 2000 May 29;92(3):178-83. doi: 10.1002/(sici)1096-8628(20000529)92:3<178::aid-ajmg4>;2-p. Am J Med Genet. 2000. PMID: 10817651
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease.
Hampe J, Lynch NJ, Daniels S, Bridger S, Macpherson AJ, Stokkers P, Forbes A, Lennard-Jones JE, Mathew CG, Curran ME, Schreiber S. Hampe J, et al. Gut. 2001 Feb;48(2):191-7. doi: 10.1136/gut.48.2.191. Gut. 2001. PMID: 11156639 Free PMC article.
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.
Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Mascheretti S, Fisher S, Frenzel H, King K, Hasselmeyer A, MacPherson AJ, Bridger S, van Deventer S, Forbes A, Nikolaus S, Lennard-Jones JE, Foelsch UR, Krawczak M, Lewis C, Schreiber S, Mathew CG. Hampe J, et al. Lancet. 2001 Jun 16;357(9272):1925-8. doi: 10.1016/S0140-6736(00)05063-7. Lancet. 2001. PMID: 11425413
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. 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.
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