Search Results - Jahn, Arne

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  1. 1
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    De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias by Harms, Frederike Leonie (Author) , Dingemans, Alexander J. M. (Author) , Hempel, Maja (Author) , Pfundt, Rolph (Author) , Bierhals, Tatjana (Author) , Casar, Christian (Author) , Müller, Christian (Author) , Niermeijer, Jikke-Mien F. (Author) , Fischer, Jan (Author) , Jahn, Arne (Author) , Hübner, Christoph (Author) , Majore, Silvia (Author) , Agolini, Emanuele (Author) , Novelli, Antonio (Author) , van der Smagt, Jasper (Author) , Ernst, Robert (Author) , van Binsbergen, Ellen (Author) , Mancini, Grazia M. S. (Author) , van Slegtenhorst, Marjon (Author) , Barakat, Tahsin Stefan (Author) , Wakeling, Emma L. (Author) , Kamath, Arveen (Author) , Downie, Lilian (Author) , Pais, Lynn (Author) , White, Susan M. (Author) , de Vries, Bert B. A. (Author) , Kutsche, Kerstin (Author) ,


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  2. 2
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    A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children by Friedrich, Ulrike A. (Author) , Bienias, Marc (Author) , Zinke, Claudia (Author) , Prazenicova, Maria (Author) , Lohse, Judith (Author) , Jahn, Arne (Author) , Menzel, Maria (Author) , Langanke, Jonas (Author) , Walter, Carolin (Author) , Wagener, Rabea (Author) , Brozou, Triantafyllia (Author) , Varghese, Julian (Author) , Dugas, Martin (Author) , Erlacher, Miriam (Author) , Schröck, Evelin (Author) , Suttorp, Meinolf (Author) , Borkhardt, Arndt (Author) , Hauer, Julia Christina (Author) , Auer, Franziska (Author) ,


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  3. 3
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    Correction: De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadias by Harms, Frederike Leonie (Author) , Dingemans, Alexander J. M. (Author) , Hempel, Maja (Author) , Pfundt, Rolph (Author) , Bierhals, Tatjana (Author) , Casar, Christian (Author) , Müller, Christian (Author) , Niermeijer, Jikke-Mien F. (Author) , Fischer, Jan (Author) , Jahn, Arne (Author) , Hübner, Christoph (Author) , Majore, Silvia (Author) , Agolini, Emanuele (Author) , Novelli, Antonio (Author) , van der Smagt, Jasper (Author) , Ernst, Robert (Author) , van Binsbergen, Ellen (Author) , Mancini, Grazia M. S. (Author) , van Slegtenhorst, Marjon (Author) , Barakat, Tahsin Stefan (Author) , Wakeling, Emma L. (Author) , Kamath, Arveen (Author) , Downie, Lilian (Author) , Pais, Lynn (Author) , White, Susan M. (Author) , de Vries, Bert B. A. (Author) , Kutsche, Kerstin (Author) ,


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  4. 4
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    Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity by Möhrmann, Lino (Author) , Werner, Maximilian (Author) , Oleś, Małgorzata (Author) , Mock, Andreas (Author) , Uhrig, Sebastian (Author) , Jahn, Arne (Author) , Kreutzfeldt, Simon (Author) , Fröhlich, Martina (Author) , Hutter, Barbara (Author) , Paramasivam, Nagarajan (Author) , Richter, Daniela (Author) , Beck, Katja (Author) , Winter, Ulrike (Author) , Pfütze, Katrin (Author) , Heilig, Christoph E. (Author) , Teleanu, Maria-Veronica (Author) , Lipka, Daniel (Author) , Zapatka, Marc (Author) , Hanf, Dorothea (Author) , List, Catrin (Author) , Allgäuer, Michael (Author) , Penzel, Roland (Author) , Rüter, Gina (Author) , Jelas, Ivan (Author) , Hamacher, Rainer W. (Author) , Falkenhorst, Johanna (Author) , Wagner, Sebastian (Author) , Brandts, Christian H. (Author) , Börries, Melanie (Author) , Illert, Anna Lena (Author) , Metzeler, Klaus H. (Author) , Westphalen, C. Benedikt (Author) , Desuki, Alexander (Author) , Kindler, Thomas (Author) , Folprecht, Gunnar (Author) , Weichert, Wilko (Author) , Brors, Benedikt (Author) , Stenzinger, Albrecht (Author) , Schröck, Evelin (Author) , Hübschmann, Daniel (Author) , Horak, Peter (Author) , Heining, Christoph (Author) , Fröhling, Stefan (Author) , Glimm, Hanno (Author) ,


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  5. 5
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    Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers by Jahn, Arne (Author) , Rump, A. (Author) , Widmann, T. J. (Author) , Heining, C. (Author) , Horak, Peter (Author) , Hutter, Barbara (Author) , Paramasivam, Nagarajan (Author) , Uhrig, Sebastian (Author) , Gieldon, Laura (Author) , Drukewitz, S. (Author) , Kübler, A. (Author) , Bermudez, M. (Author) , Hackmann, K. (Author) , Porrmann, J. (Author) , Wagner, J. (Author) , Arlt, M. (Author) , Franke, M. (Author) , Fischer, J. (Author) , Kowalzyk, Z. (Author) , William, D. (Author) , Weth, V. (Author) , Oster, S. (Author) , Fröhlich, M. (Author) , Hüllein, Jennifer (Author) , Valle González, C. (Author) , Kreutzfeldt, Simon (Author) , Mock, Andreas (Author) , Heilig, Christoph E. (Author) , Lipka, Daniel (Author) , Möhrmann, L. (Author) , Hanf, D. (Author) , Oleś, M. (Author) , Teleanu, Maria-Veronica (Author) , Allgäuer, Michael (Author) , Ruhnke, L. (Author) , Kutz, O. (Author) , Knurr, Alexander (Author) , Laßmann, Andreas (Author) , Endris, Volker (Author) , Neumann, Olaf (Author) , Penzel, Roland (Author) , Beck, K. (Author) , Richter, D. (Author) , Winter, U. (Author) , Wolf, S. (Author) , Pfütze, Katrin (Author) , Geörg, C. (Author) , Meissburger, Bettina (Author) , Buchhalter, Ivo (Author) , Augustin, M. (Author) , Aulitzky, W. E. (Author) , Hohenberger, Peter (Author) , Kroiss, M. (Author) , Schirmacher, Peter (Author) , Schlenk, Richard Friedrich (Author) , Keilholz, Ulrich (Author) , Klauschen, Frederick (Author) , Folprecht, G. (Author) , Bauer, S. (Author) , Siveke, J. T. (Author) , Brandts, C. H. (Author) , Kindler, T. (Author) , Boerries, M. (Author) , Illert, A. L. (Author) , von Bubnoff, N. (Author) , Jost, P. J. (Author) , Metzeler, K. H. (Author) , Bitzer, M. (Author) , Schulze-Osthoff, K. (Author) , Kalle, Christof von (Author) , Brors, Benedikt (Author) , Stenzinger, Albrecht (Author) , Weichert, Wilko (Author) , Hübschmann, Daniel (Author) , Fröhling, Stefan (Author) , Glimm, Hanno (Author) , Schröck, E. (Author) , Klink, Barbara (Author) ,


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  6. 6
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    Response to cabozantinib following acquired entrectinib resistance in a patient with ETV6-NTRK3 fusion-positive carcinoma harboring the NTRK3G623R solvent-front mutation by Hanf, Dorothea (Author) , Heining, Christoph (Author) , Laaber, Karin (Author) , Nebelung, Heiner (Author) , Uhrig, Sebastian (Author) , Hutter, Barbara (Author) , Jahn, Arne (Author) , Richter, Daniela (Author) , Aust, Daniela (Author) , Herbst, Friederike (Author) , Fröhling, Stefan (Author) , Glimm, Hanno (Author) , Folprecht, Gunnar (Author) ,


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  7. 7
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    Metastatic adult pancreatoblastoma: multimodal treatment and molecular characterization of a very rare disease by Berger, Anne Katrin (Author) , Mughal, Sadaf Shabbir (Author) , Allgäuer, Michael (Author) , Springfeld, Christoph (Author) , Hackert, Thilo (Author) , Weber, Tim (Author) , Naumann, Patrick (Author) , Hutter, Barbara (Author) , Horak, Peter (Author) , Jahn, Arne (Author) , Schröck, Evelin (Author) , Haag, Georg Martin (Author) , Apostolidis, Leonidas (Author) , Jäger, Dirk (Author) , Stenzinger, Albrecht (Author) , Fröhling, Stefan (Author) , Glimm, Hanno (Author) , Heining, Christoph (Author) ,


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  8. 8
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    The landscape of chromothripsis across adult cancer types by Voronina, Natalia (Author) , Wong, John K. L. (Author) , Hübschmann, Daniel (Author) , Hlevnjak, Mario (Author) , Uhrig, Sebastian (Author) , Heilig, Christoph E. (Author) , Horak, Peter (Author) , Kreutzfeldt, Simon (Author) , Mock, Andreas (Author) , Stenzinger, Albrecht (Author) , Hutter, Barbara (Author) , Fröhlich, Martina (Author) , Brors, Benedikt (Author) , Jahn, Arne (Author) , Klink, Barbara (Author) , Gieldon, Laura (Author) , Sieverling, Lina Katharine (Author) , Feuerbach, Lars (Author) , Chudasama, Priya (Author) , Beck, Katja (Author) , Kroiss, Matthias (Author) , Heining, Christoph (Author) , Möhrmann, Lino (Author) , Fischer, Andrea (Author) , Schröck, Evelin (Author) , Glimm, Hanno (Author) , Zapatka, Marc (Author) , Lichter, Peter (Author) , Fröhling, Stefan (Author) , Ernst, Aurélie (Author) ,


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  9. 9
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    Optimizing Genetic Workup in Pheochromocytoma and Paraganglioma by Integrating Diagnostic and Research Approaches by Gieldon, Laura (Author) , William, Doreen (Author) , Hackmann, Karl (Author) , Jahn, Winnie (Author) , Jahn, Arne (Author) , Wagner, Johannes (Author) , Rump, Andreas (Author) , Bechmann, Nicole (Author) , Nölting, Svenja (Author) , Knösel, Thomas (Author) , Gudziol, Volker (Author) , Constantinescu, Georgiana (Author) , Masjkur, Jimmy (Author) , Beuschlein, Felix (Author) , Timmers, Henri JLM (Author) , Canu, Letizia (Author) , Pacak, Karel (Author) , Robledo, Mercedes (Author) , Aust, Daniela (Author) , Schröck, Evelin (Author) , Eisenhofer, Graeme (Author) , Richter, Susan (Author) , Klink, Barbara (Author) ,


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  10. 10
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    ZBTB48 is both a vertebrate telomere‐binding protein and a transcriptional activator by Jahn, Arne (Author) , Buchholz, Frank (Author) ,


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