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Anzahl der Publikationen: 4
Zeitschriftenartikel
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; Rooij, Iris A. L. M. van; Blaauw, Ivo de; 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 und Schumacher, Johannes
(2022):
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.
In: Human Genetics and Genomics Advances, Bd. 3, Nr. 2, 100093
Zhang, Rong; Gehlen, Jan; Kawalia, Amit; Melissari, Maria-Theodora; Dakal, Tikam Chand; Menon, Athira M.; Hoefele, Julia; Riedhammer, Korbinian; Waffenschmidt, Lea; Fabian, Julia; Breuer, Katinka; Kalanithy, Jeshurun; Hilger, Alina Christine; Sharma, Amit; Hoelscher, Alice; Boemers, Thomas M.; Pauly, Markus; Leutner, Andreas; Fuchs, Jörg; Seitz, Guido; Ludwikowski, Barbara M.; Gomez, Barbara; Hubertus, Jochen; Heydweiller, Andreas; Kurz, Ralf; Leonhardt, Johannes; Kosch, Ferdinand; Holland-Cunz, Stefan; Muensterer, Oliver; Ure, Beno; Schmiedeke, Eberhard; Neser, Jörg; Degenhardt, Petra; Maerzheuser, Stefanie; Kleine, Katharina; Schaefer, Mattias; Spychalski, Nicole; Deffaa, Oliver J.; Gosemann, Jan-Hendrik; Lacher, Martin; Heilmann-Heimbach, Stefanie; Zwink, Nadine; Jenetzky, Ekkehart; Ludwig, Michael; Grote, Phillip; Schumacher, Johannes; Thiele, Holger und Reutter, Heiko
(2020):
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia.
In: PLOS One 15(6), e0234246 [PDF, 1MB]
In: PLOS One 15(6), e0234246 [PDF, 1MB]
Weber, Stefanie; Büscher, Anja K.; Hagmann, Henning; Liebau, Max C.; Heberle, Christian; Ludwig, Michael; Rath, Sabine; Alberer, Martin; Beissert, Antje; Zenker, Martin; Hoyer, Peter F.; Konrad, Martin; Klein, Hanns-Georg und Hoefele, Julia
(2016):
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing.
In: Pediatric Nephrology, Bd. 31, Nr. 1: S. 73-81
Degenhardt, Franziska; Heinemann, Barbara; Strohmaier, Jana; Pfohl, Marvin A.; Giegling, Ina; Hofmann, Andrea; Ludwig, Kerstin U.; Witt, Stephanie H.; Ludwig, Michael; Forstner, Andreas J.; Albus, Margot; Schwab, Sibylle G.; Borrmann-Hassenbach, Margitta; Lennertz, Leonard; Wagner, Michael; Hoffmann, Per; Rujescu, Dan; Maier, Wolfgang; Cichon, Sven; Rietschel, Marcella und Nöthen, Markus M.
(2016):
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.
In: Psychiatric Genetics, Bd. 26, Nr. 6: S. 293-296