Universität zu Köln

Juenger, Stephanie T., Andreiuolo, Felipe, Mynarek, Martin, Wohlers, Inken, Rahmann, Sven, Klein-Hitpass, Ludger, Doerner, Evelyn, zur Muehlen, Anja, Velez-Char, Natalia, von Hoff, Katja, Warmuth-Metz, Monika, Kortmann, Rolf-Dieter, Timmermann, Beate, von Bueren, Andre, Rutkowski, Stefan and Pietsch, Torsten (2020). CDKN2A deletion in supratentorial ependymoma with RELA alteration indicates a dismal prognosis: a retrospective analysis of the HIT ependymoma trial cohort. Acta Neuropathol., 140 (3). S. 405 - 408. NEW YORK: SPRINGER. ISSN 1432-0533

Juenger, Stephanie T., Mynarek, Martin, Wohlers, Inken, Doerner, Evelyn, zur Muehlen, Anja, Velez-Char, Natalia, von Hoff, Katja, Rutkowski, Stefan, Warmuth-Metz, Monika, Kortmann, Rolf-Dieter, Timmermann, Beate, Rahmann, Sven, Klein-Hitpass, Ludger, von Bueren, Andre O. and Pietsch, Torsten (2019). Improved risk-stratification for posterior fossa ependymoma of childhood considering clinical, histological and genetic features - a retrospective analysis of the HIT ependymoma trial cohort. Acta Neuropathol. Commun., 7 (1). LONDON: BMC. ISSN 2051-5960

Lindner, Sven, Bachmann, Hagen S., Odersky, Andrea, Schaefers, Simon, Klein-Hitpass, Ludger, Hero, Barbara, Fischer, Matthias, Eggert, Angelika ORCID: 0000-0003-3476-8184, Schramm, Alexander ORCID: 0000-0001-7670-7529 and Schulte, Johannes H. (2015). Absence of telomerase reverse transcriptase promoter mutations in neuroblastoma. Biomed. Rep., 3 (4). S. 443 - 447. ATHENS: SPANDIDOS PUBL LTD. ISSN 2049-9442

Molenaar, Jan J., Domingo-Fernandez, Raquel, Ebus, Marli E., Lindner, Sven, Koster, Jan ORCID: 0000-0002-0890-7585, Drabek, Ksenija, Mestdagh, Pieter, van Sluis, Peter, Valentijn, Linda J., van Nes, Johan ORCID: 0000-0001-7691-1431, Broekmans, Marloes, Haneveld, Franciska, Volckmann, Richard, Bray, Isabella, Heukamp, Lukas ORCID: 0000-0002-3388-3482, Spruessel, Annika, Thor, Theresa, Kieckbusch, Kristina, Klein-Hitpass, Ludger, Fischer, Matthias, Vandesompele, Jo ORCID: 0000-0001-6274-0184, Schramm, Alexander ORCID: 0000-0001-7670-7529, van Noesel, Max M., Varesio, Luigi, Speleman, Frank, Eggert, Angelika ORCID: 0000-0003-3476-8184, Stallings, Raymond L., Caron, Huib N., Versteeg, Rogier ORCID: 0000-0001-7172-0388 and Schulte, Johannes H. (2012). LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppression. Nature Genet., 44 (11). S. 1199 - 1207. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1546-1718

Wieczorek, Dagmar ORCID: 0000-0003-2812-6492, Boegershausen, Nina, Beleggia, Filippo ORCID: 0000-0003-0234-7094, Steiner-Haldenstaett, Sabine, Pohl, Esther, Li, Yun, Milz, Esther, Martin, Marcel ORCID: 0000-0002-0680-200X, Thiele, Holger, Altmueller, Janine, Alanay, Yasemin ORCID: 0000-0003-0683-9731, Kayserili, Hulya ORCID: 0000-0003-0376-499X, Klein-Hitpass, Ludger, Bohringer, Stefan, Wollstein, Andreas, Albrecht, Beate, Boduroglu, Koray ORCID: 0000-0001-6260-1942, Caliebe, Almuth ORCID: 0000-0003-2157-425X, Chrzanowska, Krystyna ORCID: 0000-0003-3888-0624, Cogulu, Ozgur, Cristofoli, Francesca, Czeschik, Johanna Christina ORCID: 0000-0002-9254-0084, Devriendt, Koenraad, Dotti, Maria Teresa, Elcioglu, Nursel, Gener, Blanca, Goecke, Timm O., Krajewska-Walasek, Malgorzata ORCID: 0000-0001-8721-210X, Guillen-Navarro, Encarnacion, Hayek, Joussef, Houge, Gunnar, Kilic, Esra, Simsek-Kiper, Pelin Ozlem, Lopez-Gonzalez, Vanesa, Kuechler, Alma, Lyonnet, Stanislas ORCID: 0000-0001-5426-9417, Mari, Francesca ORCID: 0000-0003-1992-1654, Marozza, Annabella, Dramard, Michele Mathieu, Mikat, Barbara, Morin, Gilles, Morice-Picard, Fanny, Ozkinay, Ferda, Rauch, Anita ORCID: 0000-0003-2930-3163, Renieri, Alessandra ORCID: 0000-0002-0846-9220, Tinschert, Sigrid, Utine, G. Eda, Vilain, Catheline, Vivarelli, Rossella, Zweier, Christiane ORCID: 0000-0001-8002-2020, Nuernberg, Peter, Rahmann, Sven, Vermeesch, Joris, Luedecke, Hermann-Josef, Zeschnigk, Michael and Wollnik, Bernd (2013). A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling. Hum. Mol. Genet., 22 (25). S. 5121 - 5136. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2083