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Marko, Hannah L., Hornig, Nadine C., Betz, Regina C., Holterhus, Paul-Martin, Altmueller, Janine, Thiele, Holger, Fabiano, Marietta 
ORCID: 0000-0002-4360-6809, Schweikert, Hans-Udo, Braun, Doreen and Schweizer, Ulrich ORCID: 0000-0003-1380-4780
(2022).
Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex development.
Hum. Mutat., 43 (3).
S. 420 - 434.
HOBOKEN:
WILEY.
ISSN 1098-1004
Rieke, Johanna Magdalena, Zhang, Rong, Braun, Doreen, Yilmaz, Oeznur, Japp, Anna S., Lopes, Filipa M., Pleschka, Michael, Hilger, Alina C., Schneider, Sophia, Newman, William G., Beaman, Glenda M., Nordenskjoeld, Agneta, Ebert, Anne-Karoline, Promm, Martin, Roesch, Wolfgang H., Stein, Raimund, Hirsch, Karin, Schaefer, Frank-Mattias, Schmiedeke, Eberhard, Boemers, Thomas M., Lacher, Martin, Kluth, Dietrich, Gosemann, Jan-Hendrik, Anderberg, Magnus, Barker, Gillian, Holmdahl, Gundela, Laeckgren, Goran, Keene, David, Cervellione, Raimondo M., Giorgio, Elisa, Di Grazia, Massimo, Feitz, Wouter F. J., Marcelis, Carlo L. M., Van Rooij, Iris A. L. M., Boekenkamp, Arend, Beckers, Goedele M. A., Keegan, Catherine E., Sharma, Amit ORCID: 0000-0002-2216-5389, Dakal, Tikam Chand, Wittler, Lars, Grote, Phillip ORCID: 0000-0002-9254-1458, Zwink, Nadine, Jenetzky, Ekkehart, Brusco, Alfredo, Thiele, Holger ORCID: 0000-0002-0169-998X, Ludwig, Michael, Schweizer, Ulrich ORCID: 0000-0003-1380-4780, Woolf, Adrian S. ORCID: 0000-0001-5541-1358, Odermatt, Benjamin and Reutter, Heiko
(2020).
SLC20A1Is Involved in Urinary Tract and Urorectal Development.
Front. Cell. Dev. Biol., 8.
LAUSANNE:
FRONTIERS MEDIA SA.
ISSN 2296-634X
Kudin, Alexei P., Baron, Gregor, Zsurka, Gabor ORCID: 0000-0002-6379-849X, Hampel, Kevin G., Elger, Christian E., Grote, Alexander, Weber, Yvonne, Lerche, Holger, Thiele, Holger, Nuernberg, Peter, Schulz, Herbert, Ruppert, Ann-Kathrin, Sander, Thomas, Cheng, Qing, Arner, Elias S. J., Schomburg, Lutz, Seeher, Sandra, Fradejas-Villar, Noelia, Schweizer, Ulrich ORCID: 0000-0003-1380-4780 and Kunz, Wolfram S. ORCID: 0000-0003-1113-3493
(2017).
Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.
Free Radic. Biol. Med., 106.
S. 270 - 278.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1873-4596