First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
Titel:
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
Auteur:
Gehlen, Jan Giel, Ann-Sophie Köllges, Ricarda Haas, Stephan L. Zhang, Rong Trcka, Jiri Sungur, Ayse Ö. Renziehausen, Florian Bornholdt, Dorothea Jung, Daphne Hoyer, Paul D. Nordenskjöld, Agneta Tibboel, Dick Vlot, John Spaander, Manon C.W. Smigiel, Robert Patkowski, Dariusz Roeleveld, Nel van Rooij, Iris ALM. de Blaauw, Ivo Hölscher, 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 Bläss, Gaby Landén, 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 Stenström, Pernilla Arnbjörnsson, Einar Frybova, Barbora Lebensztejn, Dariusz M. Debek, Wojciech Kolodziejczyk, Elwira Kozera, Katarzyna Kierkus, Jaroslaw Kaliciński, Piotr Stefanowicz, Marek Socha-Banasiak, Anna Kolejwa, Michal Piaseczna-Piotrowska, Anna Czkwianianc, Elzbieta Nöthen, 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 Małecka-Panas, Ewa Wöhr, Markus Knapp, Michael Seitz, Guido de Klein, Annelies Oracz, Grzegorz Brosens, Erwin Reutter, Heiko Schumacher, Johannes