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Plos One|January 7, 2011
The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variantsJürgen Glas, Julia Seiderer, Cornelia Tillack, et al.
Plos One|May 12, 2011
CEACAM6 gene variants in inflammatory bowel diseaseJürgen Glas, Julia Seiderer, Christoph Fries, et al.
The American Journal of Gastroenterology|March 4, 2010
Disease activity, ANCA, and IL23R genotype status determine early response to infliximab in patients with ulcerative colitisMatthias Jürgens, Rüdiger P Laubender, Franziska Hartl, et al.
Plos One|May 11, 2010
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onsetJürgen Glas, Julia Seiderer, Melinda Nagy, et al.
Journal of Gastroenterology|April 30, 2010
The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn's disease independent of the IL23R genotypeMatthias Jürgens, Stephan Brand, Rüdiger P Laubender, et al.
Inflammatory Bowel Diseases|June 29, 2006
Role of the NFKB1 -94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genesJürgen Glas, Helga-Paula Török, Laurian Tonenchi, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|March 16, 2006
IL-22 is increased in active Crohn's disease and promotes proinflammatory gene expression and intestinal epithelial cell migrationStephan Brand, Florian Beigel, Torsten Olszak, et al.
Wiener Klinische Wochenschrift|October 19, 2007
A systematic survey evaluating 6-thioguanine-related hepatotoxicity in patients with inflammatory bowel diseaseAlexander Teml, Matthias Schwab, Daan W Hommes, et al.
The American Journal of Gastroenterology|March 6, 2009
rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German populationJürgen Glas, Julia Seiderer, Giulia Pasciuto, et al.
Plos One|September 6, 2007
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variantsJürgen Glas, Julia Seiderer, Martin Wetzke, et al.
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