Database Entry Point
max planck institut
informatik
mpii logo Minerva of the Max Planck Society
 

MPI-INF D3 Publications, generated: 3:12, 19 October 2019

Search the publication database

  . Return

Your search returned the following 16 documents:

  1. David Ellinghaus, Hu Zhang, Sebastian Zeissig, Simone Lipinski, Andreas Till, Tao Jiang, Björn Stade, Yana Bromberg, Eva Ellinghaus, Andreas Keller, Manuel A. Rivas, Jurgita Skieceviciene, Nadezhda T. Doncheva, Xiao Liu, Qing Liu, Fuman Jiang, Michael Forster, Gabriele Mayr, Mario Albrecht, Robert Häsler, Bernhard O. Boehm, Jane Goodall, Carlo R. Berzuini, James Lee, Vibeke Andersen, Ulla Vogel, Limas Kupcinskas, Manfred Kayser, Michael Krawczak, Susanna Nikolaus, Rinse K. Weersma, Cyriel Y. Ponsioen, Miquel Sans, Cisca Wijmenga, David P. Strachan, Wendy L. McArdle, Séverine Vermeire, Paul Rutgeerts, Jeremy D. Sanderson, Christopher G. Mathew, Morten H. Vatn, Jun Wang, Markus M. Nöthen, Richard H. Duerr, Carsten Büning, Stephan Brand, Jürgen Glas, Juliane Winkelmann, Thomas Illig, Anna Latiano, Vito Annese, Jonas Halfvarson, Mauro D'Amato, Mark J. Daly, Michael Nothnagel, Tom H. Karlsen, Suresh Subramani, Philip Rosenstiel, Stefan Schreiber, Miles Parkes, and Andre Franke
    Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies
    Gastroenterology 145 (2): 339-347, 2013
  2. Jimmy Z. Liu, Johannes Roksund Hov, Trine Folseraas, Eva Ellinghaus, Simon M. Rushbrook, Nadezhda T. Doncheva, Ole A. Andreassen, Rinse K. Weersma, Tobias J. Weismuller, Bertus Eksteen, Pietro Invernizzi, Gideon M. Hirschfield, Daniel Nils Gotthardt, Albert Pares, David Ellinghaus, Tejas Shah, Brian D. Juran, Piotr Milkiewicz, Christian Rust, Christoph Schramm, Tobias Muller, Brijesh Srivastava, Georgios Dalekos, Markus M. Nothen, Stefan Herms, Juliane Winkelmann, Mitja Mitrovic, Felix Braun, Cyriel Y. Ponsioen, Peter J. P. Croucher, Martina Sterneck, Andreas Teufel, Andrew L. Mason, Janna Saarela, Virpi Leppa, Ruslan Dorfman, Domenico Alvaro, Annarosa Floreani, Suna Onengut-Gumuscu, Stephen S. Rich, Wesley K. Thompson, Andrew J. Schork, Sigrid Naess, Ingo Thomsen, Gabriele Mayr, Inke R. Konig, Kristian Hveem, Isabelle Cleynen, Javier Gutierrez-Achury, Isis Ricano-Ponce, David van Heel, Einar Bjornsson, Richard N. Sandford, Peter R. Durie, Espen Melum, Morten H. Vatn, Mark S. Silverberg, Richard H. Duerr, Leonid Padyukov, Stephan Brand, Miquel Sans, Vito Annese, Jean-Paul Achkar, Kirsten Muri Boberg, Hanns-Ulrich Marschall, Olivier Chazouilleres, Christopher L. Bowlus, Cisca Wijmenga, Erik Schrumpf, Severine Vermeire, Mario Albrecht, The UK-PSCSC Consortium, The International IBD Genetics Consortium, John D. Rioux, Graeme Alexander, Annika Bergquist, Judy Cho, Stefan Schreiber, Michael P. Manns, Martti Farkkila, Anders M. Dale, Roger W. Chapman, Konstantinos N. Lazaridis, The International PSC Study Group, Andre Franke, Carl A. Anderson, and Tom H. Karlsen
    Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
    Nature Genetics 45 (6): 670-677, 2013
  3. Andre Franke, Tobias Balschun, Christian Sina, David Ellinghaus, Robert Häsler, Gabriele Mayr, Mario Albrecht, Michael Wittig, Eva Buchert, Susanna Nikolaus, Christian Gieger, H. Erich Wichmann, Jurgita Sventoraityte, Limas Kupcinskas, Clive M. Onnie, Maria Gazouli, Nicholas P. Anagnou, David Strachan, Wendy L. McArdle, Christopher G. Mathew, Paul Rutgeerts, Séverine Vermeire, Morten H. Vatn, Michael Krawczak, Philip Rosenstiel, Tom H. Karlsen, and Stefan Schreiber
    Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL)
    Nature Genetics 42 (4): 292-294, 2010
  4. Eva Ellinghaus, David Ellinghaus, Philip E. Stuart, Rajan P. Nair, Sophie Debrus, John V. Raelson, Majid Belouchi, Hélène Fournier, Claudia Reinhard, Jun Ding, Yun Li, Trilokraj Tejasvi, Johann Gudjonsson, Stefan W. Stoll, John J. Voorhees, Sylviane Lambert, Stephan Weidinger, Bernadette Eberlein, Manfred Kunz, Proton Rahman, Dafna D. Gladman, Christian Gieger, H. Erich Wichmann, Tom H. Karlsen, Gabriele Mayr, Mario Albrecht, Dieter Kabelitz, Ulrich Mrowietz, Gonçalo R. Abecasis, James T. Elder, Stefan Schreiber, Michael Weichenthal, and Andre Franke
    Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2
    Nature Genetics 42 (11): 991-995, 2010
  5. Andre Franke, Tobias Balschun, Tom H. Karlsen, Jurgita Sventoraityte, Susanna Nikolaus, Gabriele Mayr, Francisco S. Domingues, Mario Albrecht, Michael Nothnagel, David Ellinghaus, Christian Sina, Clive M. Onnie, Rinse K. Weersma, Pieter C. F. Stokkers, Cisca Wijmenga, Maria Gazouli, David Strachan, Wendy L. McArdle, Séverine Vermeire, Paul Rutgeers, Philip Rosenstiel, Michael Krawczak, Morten H. Vatn, the IBSEN study group, Christopher G. Mathew, and Stefan Schreiber
    Sequence variants in IL10, ARPC2, and multiple other loci contribute to ulcerative colitis
    Nature Genetics 40 (11): 1319-1323, 2008
  6. Jochen Hampe, Andre Franke, Philip Rosenstiel, Andreas Till, Markus Teuber, Klaus Huse, Mario Albrecht, Gabriele Mayr, Francisco M. De La Vega, Jason Briggs, Simone Günther, Natalie J. Prescott, Clive M. Onnie, Robert Häsler, Bence Sipos, Ulrich R. Fölsch, Thomas Lengauer, Matthias Platzer, Christopher G. Mathew, Michael Krawczak, and Stefan Schreiber
    A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
    Nature Genetics 39 (2): 207-211, 2007
  7. Andre Franke, Jochen Hampe, Philip Rosenstiel, Christoph Becker, Florian Wagner, Robert Häsler, Randall D. Little, Klaus Huse, Andreas Ruether, Tobias Balschun, Michael Wittig, Abdou ElSharawy, Gabriele Mayr, Mario Albrecht, Natalie J. Prescott, Clive M. Onnie, Hélène Fournier, Tim Keith, Uwe Radelof, Matthias Platzer, Christopher G. Mathew, Monika Stoll, Michael Krawczak, Peter Nürnberg, and Stefan Schreiber
    Systematic association mapping identifies NELL1 as a novel IBD disease gene
    PLoS ONE 2 (8): e691.1-13, 2007
  8. Christine M. Costello, Nancy Mah, Robert Häsler, Philip Rosenstiel, Georg H. Waetzig, Andreas Hahn, Tim Lu, Yesim Gurbuz, Susanna Nikolaus, Mario Albrecht, Jochen Hampe, Ralph Lucius, Günther Klöppel, Holger Eickhoff, Hans Lehrach, Thomas Lengauer, and Stefan Schreiber
    Dissection of the inflammatory bowel disease transcriptome using genome-wide cDNA microarrays identifies novel candidate disease genes
    PLoS Medicine 2 (8): 771-787, 2005
  9. Stefan Schreiber, Philip Rosenstiel, Mario Albrecht, Jochen Hampe, and Michael Krawczak
    Genetics of Crohn disease, an archetypal inflammatory barrier disease
    Nature Reviews Genetics 6 (5): 376-388, 2005
  10. Ruta Valentonyte, Jochen Hampe, Klaus Huse, Philip Rosenstiel, Mario Albrecht, Annette Stenzel, Marion Nagy, Karoline I. Gaede, Andre Franke, Robert Haesler, Andreas Koch, Thomas Lengauer, Dirk Seegert, Norbert Reiling, Stefan Ehlers, Eberhard Schwinger, Mathias Platzer, Michael Krawczak, Joachim Müller-Quernheim, Manfred Schürmann, and Stefan Schreiber
    Sarcoidosis is associated with a truncating splice site mutation in BTNL2
    Nature Genetics 37 (4): 357-364, 2005
  11. Andreas Hahn, Christine M. Costello, Tim Lu, Thomas Lengauer, and Stefan Schreiber
    Expression analysis for inflammatory bowel disease
    In: Workshop Poster Competition, Saarbrücken, 2004
  12. Monika Stoll, Brit Corneliussen, Christine M. Costello, Georg H. Waetzig, Bjorn Mellgard, W. Andreas Koch, Philip Rosenstiel, Mario Albrecht, Peter J.P. Croucher, Dirk Seegert, Susanna Nikolaus, Jochen Hampe, Thomas Lengauer, Stefan Pierrou, Ulrich R. Foelsch, Christopher G. Mathew, Maria Lagerstrom-Fermer, and Stefan Schreiber
    Genetic variation in DLG5 is associated with inflammatory bowel disease
    Nature Genetics 36 (5): 376-380, 2004
  13. Andreas Hahn, Christine M. Costello, Tim Lu, Thomas Lengauer, and Stefan Schreiber
    Expression analysis for inflammatory bowel disease
    In: Proceedings of the n?th Conference on, 2002

  14. Mario Albrecht, Thomas Lengauer, and Stefan Schreiber
    Disease-associated variants in PYPAF1 and NOD2 result in similar alterations of conserved sequence
    Bioinformatics 19: 2171-2175, 2003. Note: In press.
  15. Mario Albrecht, Francisco S. Domingues, Stefan Schreiber, and Thomas Lengauer
    Identification of mammalian orthologs associates PYPAF5 with distinct functional roles
    FEBS Letters 538 (1-3): 173-177, 2003
  16. Mario Albrecht, Francisco S. Domingues, Stefan Schreiber, and Thomas Lengauer
    Structural localization of disease-associated sequence variations in the NACHT and LRR domains of PYPAF1 and NOD2
    FEBS Letters 554 (3): 520-528, 2003