Martin Lacher
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Mingardo E, Beaman G, Grote P, Nordenskjöld A, Newman W, Woolf A, Eckstein M, Hilger A, Dworschak G, Rösch W, Ebert A, Stein R, Brusco A, Di Grazia M, Tamer A, Torres F, Hernandez J, Erben P, Maj C, Olmos J, Riancho J, Valero C, Hostettler I, Houlden H, Werring D, Schumacher J, Gehlen J, Giel A, Buerfent B, Arkani S, Åkesson E, Rotstein E, Ludwig M, Holmdahl G, Giorgio E, Berettini A, Keene D, Cervellione R, Younsi N, Ortlieb M, Oswald J, Haid B, Promm M, Neissner C, Hirsch K, Stehr M, Schäfer F, Schmiedeke E, Boemers T, van Rooij I, Feitz W, Marcelis C, Lacher M, Nelson J, Ure B, Fortmann C, Gale D, Chan M, Ludwig K, Nöthen M, Heilmann S, Zwink N, Jenetzky E, Odermatt B, Knapp M, Reutter H. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Commun Biol 2022; 5:1203.
09.11.2022A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
09.11.2022Commun Biol 2022; 5:1203
Mingardo Enrico, Beaman Glenda, Grote Philip, Nordenskjöld Agneta, Newman William, Woolf Adrian S, Eckstein Markus, Hilger Alina C, Dworschak Gabriel C, Rösch Wolfgang, Ebert Anne-Karolin, Stein Raimund, Brusco Alfredo, Di Grazia Massimo, Tamer Ali, Torres Federico M, Hernandez Jose L, Erben Philipp, Maj Carlo, Olmos Jose M, Riancho Jose A, Valero Carmen, Hostettler Isabel, Houlden Henry, Werring David J, Schumacher Johannes, Gehlen Jan, Giel Ann-Sophie, Buerfent Benedikt C, Arkani Samara, Åkesson Elisabeth, Rotstein Emilia, Ludwig Michael, Holmdahl Gundela, Giorgio Elisa, Berettini Alfredo, Keene David, Cervellione Raimondo M, Younsi Nina, Ortlieb Melissa, Oswald Josef, Haid Bernhard, Promm Martin, Neissner Claudia, Hirsch Karin, Stehr Maximilian, Schäfer Frank-Mattias, Schmiedeke Eberhard, Boemers Thomas M, van Rooij Iris A L M, Feitz Wouter F J, Marcelis Carlo L M, Lacher Martin, Nelson Jana, Ure Benno, Fortmann Caroline, Gale Daniel P, Chan Melanie M Y, Ludwig Kerstin U, Nöthen Markus M, Heilmann Stefanie, Zwink Nadine, Jenetzky Ekkehart, Odermatt Benjamin, Knapp Michael, Reutter Heiko
Functional Toll-Like Receptor (TLR)2 polymorphisms in the susceptibility to inflammatory bowel disease
Török H, Bellon V, Konrad A, Lacher M, Tonenchi L, Siebeck M, Brand S, De Toni E. Functional Toll-Like Receptor (TLR)2 polymorphisms in the susceptibility to inflammatory bowel disease. PloS one 2017; 12:e0175180.
07.04.2017Functional Toll-Like Receptor (TLR)2 polymorphisms in the susceptibility to inflammatory bowel disease
07.04.2017PloS one 2017; 12:e0175180
Török Helga Paula, Bellon Victor, Konrad Astrid, Lacher Martin, Tonenchi Laurian, Siebeck Matthias, Brand Stephan, De Toni Enrico Narciso
Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease
Schroepf S, Koletzko S, von Schweinitz D, Berger M, Ballauff A, Helmbrecht J, Hoster E, Glas J, Lohse P, Prell C, Brand S, Kappler R, Lacher M. Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease. Inflamm Bowel Dis 2010; 16:1882-90.
01.11.2010Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease
01.11.2010Inflamm Bowel Dis 2010; 16:1882-90
Schroepf Sebastian, Koletzko Sibylle, von Schweinitz Dietrich, Berger Michael, Ballauff Antje, Helmbrecht Johanna, Hoster Eva, Glas Jürgen, Lohse Peter, Prell Christine, Brand Stephan, Kappler Roland, Lacher Martin
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
Glas J, Müller-Myhsok B, Ochsenkühn T, Göke B, Lohse P, Folwaczny M, Koletzko S, Lacher M, Schiemann U, Griga T, Epplen J, Klein W, Pfennig S, Wetzke M, Ripke S, Stallhofer J, Brand S. 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. Am J Gastroenterol 2009; 104:1737-44.
19.05.2009Novel 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
19.05.2009Am J Gastroenterol 2009; 104:1737-44
Glas Jürgen, Müller-Myhsok Bertram, Ochsenkühn Thomas, Göke Burkhard, Lohse Peter, Folwaczny Matthias, Koletzko Sibylle, Lacher Martin, Schiemann Uwe, Griga Thomas, Epplen Jörg T, Klein Wolfram, Pfennig Simone, Wetzke Martin, Ripke Stephan, Stallhofer Johannes, Brand Stephan