Russell, Claire, Issler, Naomi, Afonso, Sara, Ziegler, Christine, Weissman, Irith, Dumitriu, Simona, Lowe, Martin, Jordan, Katrin, Iancu, Daniela, Davies, Benjamin, Cebrian-Serrano, Alberto, Tekman, Mehmet, Böckenhauer, Detlef, Warth, Richard, Kleta, Robert, Zaccai, Tzipora C.  Falik, Meindl, Katrin, Stanescu, Horia C., Dahlke, Eileen, Klootwijk, Enriko D., Tziridis, Konstantin, Yan, Guanhua, Kesselheim, Anne, Patel, Vaksha, Robles-López, José M., Tabernero, Lydia, Schulze, Holger, Mozere, Monika, Anikster, Yair, Magen, Daniella, Jaureguiberry, Graciana, Ben Izhak, Ofer, Arnon-Sheleg, Elite, Outtandy, Priya, Fedida, Ayalla, Forst, Anna-Lena, Kalfon, Limor, Sterner, Christina, Biton, Efrat Shuster, Heinl, Elena-Sofia, Othmen, Helga, Tegtmeier, Ines, Reichold, Markus, Schiessl, Ina Maria, Limm, Katharina, Oefner, Peter, Witzgall, Ralph, Fu, Lifei, Theilig, Franziska, Schilling, Achim, "A founder mutation in EHD1 presents with tubular proteinuria and deafness", ,