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Transforming Growth Factor β1 and Gap Junction Protein Alpha 4 Gene Heterogeneity in Relation to the Severity of Clinical Disease in Cystic Fibrosis Laubach, Joern Pascal; Ludwig, Michael; Horn, Tabea; Eickmeier, Olaf; Smaczny, Christina; Schubert, Ralf; Zielen, Stefan; Majoor, Christof; Aydin, Malik; Schnell, Alexander; Schmitt-Grohe, Sabina 分享 收藏
Mannose-Binding Lectin (MBL) and Gap Junction Protein Alpha 4 (GJA4) Gene Heterogeneity in Relation to Severity of Clinical Disease in Cystic Fibrosis Laubach, Joern Pascal; Ludwig, Michael; Horn, Tabea; Eickmeier, Olaf; Smaczny, Christina; Schubert, Ralf; Zielen, Stefan; Majoor, Christof; Aydin, Malik; Schmitt-Grohe, Sabina 分享 收藏
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B Gehlen, Jan; Giel, Ann-Sophie; Koellges, Ricarda; Haas, Stephan L.; Zhang, Rong; Trcka, Jiri; Sungur, Ayse O.; Renziehausen, Florian; Bornholdt, Dorothea; Jung, Daphne; Hoyer, Paul D.; Nordenskjold, Agneta; Tibboel, Dick; Vlot, John; Spaander, Manon C. W.; Smigiel, Robert; Patkowski, Dariusz; Roeleveld, Nel; van Rooij, Iris Alm; de Blaauw, Ivo; Hoelscher, Alice; Pauly, Marcus; Leutner, Andreas; Fuchs, Joerg; Niethammer, Joel; Melissari, Maria-Theodora; Jenetzky, Ekkehart; Zwink, Nadine; Thiele, Holger; Hilger, Alina Christine; Hess, Timo; Trautmann, Jessica; Marks, Matthias; Baumgarten, Martin; Blaess, Gaby; Landen, Mikael; Fundin, Bengt; Bulik, Cynthia M.; Pennimpede, Tracie; Ludwig, Michael; Ludwig, Kerstin U.; Mangold, Elisabeth; Heilmann-Heimbach, Stefanie; Moebus, Susanne; Herrmann, Bernhard G.; Alsabeah, Kristina; Burgos, Carmen M.; Lilja, Helene E.; Azodi, Sahar; Stenstrom, Pernilla; Arnbjornsson, Einar; Frybova, Barbora; Lebensztejn, Dariusz M.; Debek, Wojciech; Kolodziejczyk, Elwira; Kozera, Katarzyna; Kierkus, Jaroslaw; Kalicinski, Piotr; Stefanowicz, Marek; Socha-Banasiak, Anna; Kolejwa, Michal; Piaseczna-Piotrowska, Anna; Czkwianianc, Elzbieta; Noethen, Markus M.; Grote, Phillip; Rygl, Michal; Reinshagen, Konrad; Spychalski, Nicole; Ludwikowski, Barbara; Hubertus, Jochen; Heydweiller, Andreas; Ure, Benno; Muensterer, Oliver J.; Aubert, Ophelia; Gosemann, Jan-Hendrik; Lacher, Martin; Degenhardt, Petra; Boemers, Thomas M.; Mokrowiecka, Anna; Malecka-Panas, Ewa; Woehr, Markus; Knapp, Michael; Seitz, Guido; de Klein, Annelies; Oracz, Grzegorz; Brosens, Erwin; Reutter, Heiko; Schumacher, Johannes 分享 收藏
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Detection of meticillin-resistant Staphylococcus aureus and carbapenemase-producing Enterobacteriaceae in Danish emergency departments - evaluation of national screening guidelines Skjot-Arkil, H.; Mogensen, C. B.; Lassen, A. T.; Johansen, I. S.; Chen, M.; Petersen, P.; Andersen, K., V; Ellermann-Eriksen, S.; Moller, J. M.; Ludwig, M.; Fuglsang-Damgaard, D.; Nielsen, F. E.; Petersen, D. B.; Jensen, U. S.; Rosenvinge, F. S. 分享 收藏
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction Kolvenbach, Caroline M.; Dworschak, Gabriel C.; Frese, Sandra; Japp, Anna S.; Schuster, Peggy; Wenzlitschke, Nina; Yilmaz, Oeznur; Lopes, Filipa M.; Pryalukhin, Alexey; Schierbaum, Luca; van der Zanden, Loes F. M.; Kause, Franziska; Schneider, Ronen; Taranta-Janusz, Katarzyna; Szczepanska, Maria; Pawlaczyk, Krzysztof; Newman, William G.; Beaman, Glenda M.; Stuart, Helen M.; Cervellione, Raimondo M.; Feitz, Wouter F. J.; van Rooij, Iris A. L. M.; Schreuder, Michiel F.; Steffens, Martijn; Weber, Stefanie; Merz, Waltraut M.; Feldkoetter, Markus; Hoppe, Bernd; Thiele, Holger; Altmueller, Janine; Berg, Christoph; Kristiansen, Glen; Ludwig, Michael; Reutter, Heiko; Woolf, Adrian S.; Hildebrandt, Friedhelm; Grote, Phillip; Zaniew, Marcin; Odermatt, Benjamin; Hilger, Alina C. 分享 收藏
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ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development Zhang, Rong; Knapp, Michael; Suzuki, Kentaro; Kajioka, Daiki; Schmidt, Johanna M.; Winkler, Jonas; Yilmaz, Oeznur; Pleschka, Michael; Cao, Jia; Kockum, Christina Clementson; Barker, Gillian; Holmdahl, Gundela; Beaman, Glenda; Keene, David; Woolf, Adrian S.; Cervellione, Raimondo M.; Cheng, Wei; Wilkins, Simon; Gearhart, John P.; Sirchia, Fabio; Di Grazia, Massimo; Ebert, Anne-Karolin; Roesch, Wolfgang; Ellinger, Joerg; Jenetzky, Ekkehart; Zwink, Nadine; Feitz, Wout F.; Marcelis, Carlo; Schumacher, Johannes; Martinon-Torres, Federico; Hibberd, Martin Lloyd; Khor, Chiea Chuen; Heilmann-Heimbach, Stefanie; Barth, Sandra; Boyadjiev, Simeon A.; Brusco, Alfredo; Ludwig, Michael; Newman, William; Nordenskjold, Agneta; Yamada, Gen; Odermatt, Benjamin; Reutter, Heiko 分享 收藏
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs Schumann, Madita; Hofmann, Andrea; Krutzke, Sophia K.; Hilger, Alina C.; Marsch, Florian; Stienen, Dietlinde; Gembruch, Ulrich; Ludwig, Michael; Merz, Waltraut M.; Reutter, Heiko 分享 收藏
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association Hilger, Alina C.; Halbritter, Jan; Pennimpede, Tracie; van der Ven, Amelie; Sarma, Georgia; Braun, Daniela A.; Porath, Jonathan D.; Kohl, Stefan; Hwang, Daw-Yang; Dworschak, Gabriel C.; Hermann, Bernhard G.; Pavlova, Anna; El-Maarri, Osman; Noethen, Markus M.; Ludwig, Michael; Reutter, Heiko; Hildebrandt, Friedhelm 分享 收藏
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish Korberg, Izabella Baranowska; Hofmeister, Wolfgang; Markljung, Ellen; Cao, Jia; Nilsson, Daniel; Ludwig, Michael; Draaken, Markus; Holmdahl, Gundela; Barker, Gillian; Reutter, Heiko; Vukojevic, Vladana; Kockum, Christina Clementson; Lundin, Johanna; Lindstrand, Anna; Nordenskjold, Agneta 分享 收藏
Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy Draaken, Markus; Knapp, Michael; Pennimpede, Tracie; Schmidt, Johanna M.; Ebert, Anne-Karolin; Roesch, Wolfgang; Stein, Raimund; Utsch, Boris; Hirsch, Karin; Boemers, Thomas M.; Mangold, Elisabeth; Heilmann, Stefanie; Ludwig, Kerstin U.; Jenetzky, Ekkehart; Zwink, Nadine; Moebus, Susanne; Herrmann, Bernhard G.; Mattheisen, Manuel; Noethen, Markus M.; Ludwig, Michael; Reutter, Heiko 分享 收藏
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Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder Reutter, Heiko; Draaken, Markus; Pennimpede, Tracie; Wittler, Lars; Brockschmidt, Felix F.; Ebert, Anne-Karolin; Bartels, Enrika; Roesch, Wolfgang; Boemers, Thomas M.; Hirsch, Karin; Schmiedeke, Eberhard; Meesters, Christian; Becker, Tim; Stein, Raimund; Utsch, Boris; Mangold, Elisabeth; Nordenskjoeld, Agneta; Barker, Gillian; Kockum, Christina Clementsson; Zwink, Nadine; Holmdahl, Gundula; Laeckgren, Goeran; Jenetzky, Ekkehart; Feitz, Wouter F. J.; Marcelis, Carlo; Wijers, Charlotte H. W.; Van Rooij, Iris A. L. M.; Gearhart, John P.; Herrmann, Bernhard G.; Ludwig, Michael; Boyadjiev, Simeon A.; Noethen, Markus M.; Mattheisen, Manuel 分享 收藏
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Effect of Genetic Variation in a Drosophila Model of Diabetes-Associated Misfolded Human Proinsulin He, Bin Z.; Ludwig, Michael Z.; Dickerson, Desiree A.; Barse, Levi; Arun, Bharath; Vilhjalmsson, Bjarni J.; Park, Soo-Young; Tamarina, Natalia A.; Selleck, Scott B.; Wittkopp, Patricia J.; Bell, Graeme I.; Kreitman, Martin 分享 收藏
Genetic Complexity in a Drosophila Model of Diabetes-Associated Misfolded Human Proinsulin Park, Soo-Young; Ludwig, Michael Z.; Tamarina, Natalia A.; He, Bin Z.; Carl, Sarah H.; Dickerson, Desiree A.; Barse, Levi; Arun, Bharath; Williams, Calvin L.; Miles, Cecelia M.; Philipson, Louis H.; Steiner, Donald F.; Bell, Graeme I.; Kreitman, Martin 分享 收藏
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