Items where Author is "Wagner, Matias"

2021

Vavassori, Stefano and Chou, Janet and Faletti, Laura Eva and Haunerdinger, Veronika and Opitz, Lennart and Joset, Pascal and Fraser, Christopher J. and Prader, Seraina and Gao, Xianfei and Schuch, Luise A. and Wagner, Matias and Hoefele, Julia and Maccari, Maria Elena and Zhu, Ying and Elakis, George and Gabbett, Michael T. and Forstner, Maria and Omran, Heymut and Kaiser, Thomas and Kessler, Christina and Olbrich, Heike and Frosk, Patrick and Almutairi, Abduarahman and Platt, Craig D. and Elkins, Megan and Weeks, Sabrina and Rubin, Tamar and Planas, Raquel and Marchetti, Tommaso and Koovely, Danil and Klämbt, Verena and Soliman, Neveen A. and von Hardenberg, Sandra and Klemann, Christian and Baumann, Ulrich and Lenz, Dominic and Klein-Franke, Andreas and Schwemmle, Martin and Huber, Michael and Sturm, Ekkehard and Hartleif, Steffen and Häffner, Karsten and Gimpel, Charlotte and Brotschi, Barbara and Laube, Guido and Güngör, Tayfun and Buckley, Michael F. and Kottke, Raimund and Staufner, Christian and Hildebrandt, Friedhelm and Reu-Hofer, Simone and Moll, Solange and Weber, Achim and Kaur, Hundeep and Ehl, Stephan and Hiller, Sebastian and Geha, Raif and Roscioli, Tony and Griese, Matthias and Pachlopnik Schmid, Jana. (2021) Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency. The Journal of Allergy & Clinical Immunology, 148 (2). pp. 381-393.

2020

Ascari, Giulia and Peelman, Frank and Farinelli, Pietro and Rosseel, Toon and Lambrechts, Nina and Wunderlich, Kirsten A. and Wagner, Matias and Nikopoulos, Konstantinos and Martens, Pernille and Balikova, Irina and Derycke, Lara and Holtappels, Gabriële and Krysko, Olga and Van Laethem, Thalia and De Jaegere, Sarah and Guillemyn, Brecht and De Rycke, Riet and De Bleecker, Jan and Creytens, David and Van Dorpe, Jo and Gerris, Jan and Bachert, Claus and Neuhofer, Christiane and Walraedt, Sophie and Bischoff, Almut and Pedersen, Lotte B. and Klopstock, Thomas and Rivolta, Carlo and Leroy, Bart P. and De Baere, Elfride and Coppieters, Frauke. (2020) Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility. Human mutation, 41 (5). pp. 998-1011.