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Number of items: 7.

Journal Article

Bauer, Peter, Bretz, Frank, Dragalin, Vladimir, Koenig, Franz and Wassmer, Gernot (2016). Authors' response to comments. Stat. Med., 35 (3). S. 364 - 368. HOBOKEN: WILEY. ISSN 1097-0258

Bauer, Peter, Bretz, Frank ORCID: 0000-0002-2008-8340, Dragalin, Vladimir, Koenig, Franz and Wassmer, Gernot (2016). Twenty-five years of confirmatory adaptive designs: opportunities and pitfalls. Stat. Med., 35 (3). S. 325 - 348. HOBOKEN: WILEY. ISSN 1097-0258

Bauer, Peter, Hunimel, Michael, von Kalle, Christof, Schmutzler, Rita, Block, Andreas, Stroth, Matthias, Woopen, Christiane and Engelke, Karsten (2016). Molecular Genetic Diagnosis - What we do know about Machines? What we do want to know? Oncol. Res. Treat., 39. S. 3 - 25. BASEL: KARGER. ISSN 2296-5262

Guenther, Sven, Elert-Dobkowska, Ewelina, Soehn, Anne S., Hinreiner, Sophie, Yoon, Grace, Heller, Raoul, Hellenbroich, Yorck, Huebner, Christian A., Ray, Peter N., Hehr, Ute, Bauer, Peter, Sulek, Anna ORCID: 0000-0003-2975-4888 and Beetz, Christian ORCID: 0000-0001-7061-2895 (2016). High Frequency of Pathogenic Rearrangements in SPG11 and Extensive Contribution of Mutational Hotspots and Founder Alleles. Hum. Mutat., 37 (7). S. 703 - 710. HOBOKEN: WILEY. ISSN 1098-1004

Minnerop, Martina, Kurzwelly, Delia, Wagner, Holger, Soehn, Anne S., Reichbauer, Jennifer, Tao, Feifei, Rattay, Tim W. ORCID: 0000-0002-5456-7761, Peitz, Michael, Rehbach, Kristina, Giorgetti, Alejandro, Pyle, Angela, Thiele, Holger, Altmueller, Janine, Timmann, Dagmar, Karaca, Ilker, Lennarz, Martina, Baets, Jonathan, Hengel, Holger, Synofzik, Matthis, Atasu, Burcu, Feely, Shawna, Kennerson, Marina, Stendel, Claudia, Lindig, Tobias, Gonzalez, Michael A., Stirnberg, Ruediger, Sturm, Marc ORCID: 0000-0002-6552-8362, Roeske, Sandra, Jung, Johanna, Bauer, Peter, Lohmann, Ebba, Herms, Stefan ORCID: 0000-0002-2786-8200, Heilmann-Heimbach, Stefanie ORCID: 0000-0003-1057-465X, Nicholson, Garth, Mahanjah, Muhammad, Sharkia, Rajech, Carloni, Paolo, Bruestle, Oliver, Klopstock, Thomas, Mathews, Katherine D., Shy, Michael E., de Jonghe, Peter, Chinnery, Patrick F., Horvath, Rita ORCID: 0000-0002-9841-170X, Kohlhase, Juergen, Schmitt, Ina, Wolf, Michael, Greschus, Susanne, Amunts, Katrin, Maier, Wolfgang, Schoels, Ludger, Nuernberg, Peter, Zuchner, Stephan, Klockgether, Thomas, Ramirez, Alfredo ORCID: 0000-0003-4991-763X and Schuele, Rebecca (2017). Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. Brain, 140. S. 1561 - 1579. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Miranda, Marcelo, Harmuth, Florian, Leonor Bustamante, M., Rossi, Malco, Sturm, Marc ORCID: 0000-0002-6552-8362, Magnusson, Olafur Th, Bauer, Peter, Klockgether, Thomas and Ramirez, Alfredo ORCID: 0000-0003-4991-763X (2020). Intermediate phenotype of ATP13A2 mutation in two Chilean siblings: Towards a continuum between parkinsonism and hereditary spastic paraplegia. Parkinsonism Relat. Disord., 81. S. 45 - 48. OXFORD: ELSEVIER SCI LTD. ISSN 1873-5126

Sepahi, Ilnaz, Faust, Ulrike, Sturm, Marc ORCID: 0000-0002-6552-8362, Bosse, Kristin, Kehrer, Martin, Heinrich, Tilman, Grundman-Hauser, Kathrin, Bauer, Peter, Ossowski, Stephan, Susak, Hana ORCID: 0000-0002-7965-7675, Varon, Raymonda, Schroeck, Evelin, Niederacher, Dieter, Auber, Bernd, Sutter, Christian, Arnold, Norbert ORCID: 0000-0003-4523-8808, Hahnen, Eric, Dworniczak, Bernd, Wang-Gorke, Shan, Gehrig, Andrea, Weber, Bernhard H. F., Engel, Christoph ORCID: 0000-0002-7247-282X, Lemke, Johannes R., Hartkopf, Andreas, Riess, Olaf and Schroeder, Christopher (2019). Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women. BMC Cancer, 19 (1). LONDON: BMC. ISSN 1471-2407

This list was generated on Thu Mar 28 20:09:20 2024 CET.