Universität zu Köln

Journal Article

Kause, Franziska, Reutter, Heiko, Marsch, Florian, Thiele, Holger, Altmueller, Janine, Ludwig, Michael and Zhang, Rong (2018). Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio-otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance? Mol. Med. Rep., 17 (2). S. 3200 - 3206. ATHENS: SPANDIDOS PUBL LTD. ISSN 1791-3004

Kause, Franziska ORCID: 0000-0002-0074-8962, Zhang, Rong, Ludwig, Michael, Schmiedeke, Eberhard, Rissmann, Anke, Thiele, Holger, Altmueller, Janine, Herms, Stefan, Hilger, Mina C., Hildebrandt, Friedhelm and Reutter, Heiko (2019). HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Res., 111 (10). S. 591 - 598. HOBOKEN: WILEY. ISSN 2472-1727

Todd, William D., Fenselau, Henning, Wang, Joshua L., Zhang, Rong ORCID: 0000-0001-7906-6210, Machado, Natalia L., Venner, Anne ORCID: 0000-0001-7481-3248, Broadhurst, Rebecca Y., Kaur, Satvinder, Lynagh, Timothy ORCID: 0000-0003-4888-4098, Olson, David P., Lowell, Bradford B., Fuller, Patrick M. and Saper, Clifford B. (2018). A hypothalamic circuit for the circadian control of aggression. Nat. Neurosci., 21 (5). S. 717 - 728. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1546-1726

Weitensteiner, Valerie, Zhang, Rong, Bungenberg, Julia, Marks, Matthias, Gehlen, Jan, Ralser, Damian J., Hilger, Alina C., Sharma, Amit ORCID: 0000-0002-2216-5389, Schumacher, Johannes, Gembruch, Ulrich ORCID: 0000-0001-8284-4669, Merz, Waltraut M., Becker, Albert, Altmueller, Janine, Thiele, Holger, Herrmann, Bernhard G., Odermatt, Benjamin, Ludwig, Michael and Reutter, Heiko (2018). Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth Defects Res., 110 (7). S. 587 - 598. HOBOKEN: WILEY. ISSN 2472-1727

Zhang, Rong, Marsch, Florian, Kause, Franziska, Degenhardt, Franziska, Schmiedeke, Eeberhard, Maerzheuser, Stefanie, Hoppe, Bernd, Bachour, Haitham, Boemers, Thomas M., Schaefer, Matthias, Spychalski, Nicole, Neser, Joerg, Leonhardt, Johannes, Kosch, Ferdinand, Ure, Benno, Gomez, Barbara, Lacher, Martin, Deffaa, Oliver J., Palta, Markus, Wittekindt, Boris, Kleine, Katharina, Schmedding, Andrea ORCID: 0000-0002-7796-3329, Grasshoff-Derr, Sabine, van der Ven, Amelie, Heilmann-Heimbach, Stefanie ORCID: 0000-0003-1057-465X, Zwink, Nadine, Jenetzky, Ekkehart ORCID: 0000-0001-5415-8784, Ludwig, Michael and Reutter, Heiko ORCID: 0000-0002-3591-5265 (2017). Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations. Birth Defects Res., 109 (13). S. 1063 - 1070. HOBOKEN: WILEY. ISSN 2472-1727

Zhang, Rong, Thiele, Holger, Bartmann, Peter, Hilger, Alina C., Berg, Christoph, Herberg, Ulrike, Klingmueller, Dietrich, Nuernberg, Peter, Ludwig, Michael and Reutter, Heiko (2016). Whole-Exome Sequencing in Nine Monozygotic Discordant Twins. Twin Res. Hum. Genet., 19 (1). S. 60 - 66. NEW YORK: CAMBRIDGE UNIV PRESS. ISSN 1839-2628