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Wolfram Klein

Ruhr University Bochum

65

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1578

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P230 - Ethnic differences in the genetic susceptibility to Crohn's disease: functional PPARγ gene variants are not associated with susceptibility to inflammatory bowel disease in the German population

2009 Journal of Crohns & Colitis
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P216 - The first two Crohn's disease susceptibility loci with a high degree of epistasis: PTGER4-expression-modulating polymorphisms in the 5p13.1 region enhance ATG16L1-associated susceptibility to Crohn's disease

2009 Journal of Crohns & Colitis
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P253 - The role of pregnane X receptor (PXR/NR1I2) gene variants in inflammatory bowel disease

2009 Journal of Crohns & Colitis
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P220 - The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery

2009 Journal of Crohns & Colitis
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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

2009 The American Journal of Gastroenterology
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M2046 Significant Differences in the Genetic Susceptibility to Crohn's Disease Between North American and European Populations Regarding Gene Variants in Phox2b, Ncf4, Fam92b, and in the Intergenic Region On Chromosome 10q21.1

2008 Gastroenterology
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Analysis of pregnane X receptor (PXR/NR1I2) gene variants in inflammatory bowel disease

2008 Zeitschrift Fur Gastroenterologie
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Novel protective markers for ulcerative colitis in the IL2/IL21 region suggest a common genetic background for ulcerative colitis and celiac disease

2008 Zeitschrift Fur Gastroenterologie
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M2042 The Role of Pregnane X Receptor (PXR/NR1i2) Gene Variants in Inflammatory Bowel Disease

2008 Gastroenterology
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The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery

2008 Zeitschrift Fur Gastroenterologie
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