Glas, J., J. Seiderer, J. Wagner, T. Olszak, C. Fries, C. Tillack, M. Friedrich, F. Beigel, J. Stallhofer, C. Steib, M. Wetzke, B. Göke, T. Ochsenkühn, J. Diegelmann, D. Czamara and S. Brand: Analysis of IL12B Gene Variants in Inflammatory Bowel Disease. In: PLoS ONE 7, 3, Seq. No.: e34349 (2012).
Glas, J., J. Wagner, J. Seiderer, T. Olszak, M. Wetzke, F. Beigel, C. Tillack, J. Stallhofer, M. Friedrich, C. Steib, B. Göke, T. Ochsenkühn, N. Karbalai, J. Diegelmann, D. Czamara and S. Brand: PTPN2 Gene Variants Are Associated with Susceptibility to Both Crohn's Disease and Ulcerative Colitis Supporting a Common Genetic Disease Background. In: PLoS ONE 7, 3, Seq. No.: e33682 (2012).
Glas, J., J. Seiderer, D. Fischer, B. Tengler, S. Pfennig, M. Wetzke, F. Beigel, T. Olszak, M. Weidinger, B. Göke, T. Ochsenkühn, M. Folwaczny, B. Müller-Myhsok, J. Diegelmann, D. Czamara and S. Brand: Pregnane X Receptor (PXR/NR1I2) Gene Haplotypes Modulate Susceptibility to Inflammatory Bowel Disease. In: Inflammatory Bowel Diseases 17, 9, 1917-1924 (2011).
Glas, J., J. Seiderer, C. Fries, C. Tillack, S. Pfennig, M. Weidinger, F. Beigel, T. Olszak, U. Lass, B. Göke, T. Ochsenkühn, C. Wolf, P. Lohse, B. Müller-Myhsok, J. Diegelmann, D. Czamara and S. Brand: CEACAM6 Gene Variants in Inflammatory Bowel Disease. In: PLoS ONE 6, 4, Seq. No.: e19319 (2011).
Glas, J., J. Seiderer, C. Markus, S. Pfennig, M. Wetzke, E. Paschos, B. Göke, T. Ochsenkühn, B. Müller-Myhsok, J. Diegelmann, D. Roeske and S. Brand: Role of PPARG Gene Variants in Inflammatory Bowel Disease. In: Inflammatory Bowel Diseases 17, 4, 1057-1058 (2011).
Glas, J., J. Seiderer, C. Tillack, S. Pfennig, F. Beigel, M. Jürgens, T. Olszak, R. P. Laubender, M. Weidinger, B. Müller-Myhsok, B. Göke, T. Ochsenkühn, P. Lohse, J. Diegelmann, D. Czamara and S. Brand: The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants. In: PLoS ONE 5, 12, Seq. No.: e14466 (2010).
Glas, J., J. Seiderer, M. Nagy, C. Fries, F. Beigel, M. Weidinger, S. Pfennig, W. Klein, J. T. Epplen, P. Lohse, M. Folwaczny, B. Göke, T. Ochsenkühn, J. Diegelmann, B. Müller-Myhsok, D. Roeske and S. Brand: Evidence for STAT4 as a Common Autoimmune Gene: rs7574865 Is Associated with Colonic Crohn's Disease and Early Disease Onset. In: PLoS ONE 5, 4, Seq. No.: doi:10.1371/journal.pone.0010373 (2010).
Glas, J. N., J. Stallhofer, S. Ripke, M. Wetzke, S. Pfennig, W. Klein, J. T. Epplen, T. Griga, U. Schiemann, M. Lacher, S. Koletzko, M. Folwaczny, P. Lohse, B. Göke, T. Ochsenkühn, B. Müller-Myhsok and S. Brand: 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. In: American Journal of Gastroenterology 104, 7, 1737-1744 (2009).
Glas, J., J. Seiderer, G. Pasciuto, C. Tillack, J. Diegelmann, S. Pfennig, A. Konrad, S. Schmechel, M. Wetzke, H. P. Torok, J. Stallhofer, M. Jürgens, T. Griga, W. Klein, J. T. Epplen, U. Schiemann, T. Mussack, P. Lohse, B. Göke, T. Ochsenkühn, M. Folwaczny, B. Müller-Myhsok and S. Brand: 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. In: American Journal of Gastroenterology 104, 3, 665-672 (2009).
Seiderer, J., J. Dambacher, D. Leistner, C. Tillack, J. Glas, J. H. Niess, S. Pfennig, M. Jürgens, B. Müller-Myhsok, B. Göke, T. Ochsenkühn, P. Lohse, H. C. Reinecker and S. Brand: Genotype-phenotype analysis of the CXCL 16 p.Ala181Val polymorphism in inflammatory bowel disease. In: Clinical Immunology 127, 1, 49-55 (2008).
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.