Publications by authors named "Simone Pfennig"

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Pregnane X receptor (PXR/NR1I2) gene haplotypes modulate susceptibility to inflammatory bowel disease.
Jürgen Glas, Julia Seiderer, Daniel Fischer, Barbara Tengler, Simone Pfennig

Inflamm Bowel Dis· September 2011

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Role of PPARG gene variants in inflammatory bowel disease.
Jürgen Glas, Julia Seiderer, Christian Markus, Simone Pfennig, Martin Wetzke

Inflamm Bowel Dis· April 2011

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CEACAM6 gene variants in inflammatory bowel disease.
Jürgen Glas, Julia Seiderer, Christoph Fries, Cornelia Tillack, Simone Pfennig

PLoS One· April 2011

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Formation of antinuclear and double-strand DNA antibodies and frequency of lupus-like syndrome in anti-TNF-α antibody-treated patients with inflammatory bowel disease.
Florian Beigel, Fabian Schnitzler, Rüdiger Paul Laubender, Simone Pfennig, Maria Weidinger

Inflamm Bowel Dis· January 2011

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The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.
Jürgen Glas, Julia Seiderer, Cornelia Tillack, Simone Pfennig, Florian Beigel

PLoS One· December 2010

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Disease activity, ANCA, and IL23R genotype status determine early response to infliximab in patients with ulcerative colitis.
Matthias Jürgens, Rüdiger P Laubender, Franziska Hartl, Maria Weidinger, Julia Seiderer, Simone Pfennig

Am J Gastroenterol· August 2010

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The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn's disease independent of the IL23R genotype.
Matthias Jürgens, Stephan Brand, Rüdiger P Laubender, Julia Seiderer, Jürgen Glas, Simone Pfennig

J Gastroenterol· July 2010

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Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
Jürgen Glas, Julia Seiderer, Melinda Nagy, Christoph Fries, Florian Beigel, Simone Pfennig

PLoS One· April 2010

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The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease.
Martin Storr, Dominik Emmerdinger, Julia Diegelmann, Simone Pfennig, Thomas Ochsenkühn

PLoS One· February 2010

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Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease.
Jürgen Glas, Johannes Stallhofer, Stephan Ripke, Martin Wetzke, Simone Pfennig

Am J Gastroenterol· July 2009

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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 population.
Jürgen Glas, Julia Seiderer, Giulia Pasciuto, Cornelia Tillack, Julia Diegelmann, Simone Pfennig

Am J Gastroenterol· March 2009

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Role of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD.
Julia Seiderer, Ira Elben, Julia Diegelmann, Jürgen Glas, Johannes Stallhofer, Simone Pfennig

Inflamm Bowel Dis· April 2008

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Genotype-phenotype analysis of the CXCL16 p.Ala181Val polymorphism in inflammatory bowel disease.
Julia Seiderer, Julia Dambacher, Dorothea Leistner, Cornelia Tillack, Jürgen Glas, Simone Pfennig

Clin Immunol· April 2008

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The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
Jürgen Glas, Astrid Konrad, Silke Schmechel, Julia Dambacher, Julia Seiderer, Simone Pfennig

Am J Gastroenterol· March 2008

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rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
Jürgen Glas, Julia Seiderer, Martin Wetzke, Astrid Konrad, Helga-Paula Török, Simone Pfennig

PLoS One· September 2007

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Macrophage migration inhibitory factor (MIF) -173G/C promoter polymorphism influences upper gastrointestinal tract involvement and disease activity in patients with Crohn's disease.
Julia Dambacher, Tanja Staudinger, Julia Seiderer, Zeljka Sisic, Fabian Schnitzler, Simone Pfennig

Inflamm Bowel Dis· January 2007

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Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis.
Julia Seiderer, Fabian Schnitzler, Stephan Brand, Tanja Staudinger, Simone Pfennig

Scand J Gastroenterol· December 2006

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Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: results of a prospective study.
Julia Seiderer, Stephan Brand, Karin A Herrmann, Fabian Schnitzler, Rudolf Hatz, Simone Pfennig

Inflamm Bowel Dis· December 2006

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Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease.
Fabian Schnitzler, Stephan Brand, Tanja Staudinger, Simone Pfennig, Katrin Hofbauer

Immunogenetics· April 2006

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Increased expression of the chemokine fractalkine in Crohn's disease and association of the fractalkine receptor T280M polymorphism with a fibrostenosing disease Phenotype.
Stephan Brand, Katrin Hofbauer, Julia Dambacher, Fabian Schnitzler, Tanja Staudinger, Simone Pfennig

Am J Gastroenterol· January 2006

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The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.
Stephan Brand, Tanja Staudinger, Fabian Schnitzler, Simone Pfennig, Katrin Hofbauer

Inflamm Bowel Dis· July 2005

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