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Number of items: 7.

Journal Article

Hahnen, Eric, Baumann, Klaus H., Heimbach, Andre, Reuss, Alexander, Jackisch, Christian, Hauke, Jan, Park-Simon, Tjoung-Won, Richters, Lisa Katharina, Hanker, Lars Christian, Kroeber, Sandra, Pfisterer, Jacobus, Gevensleben, Heidrun, Schnelzer, Andreas, Dietrich, Dimo, Schneider, Stephanie, Kommoss, Stefan, Marme, Frederic, Prieske, Katharina, Schmutzler, Rita K. and Harter, Philipp (2016). Prevalence of somatic mutations in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1 study). J. Clin. Oncol., 34 (15). ALEXANDRIA: AMER SOC CLINICAL ONCOLOGY. ISSN 1527-7755

Harter, Philipp, Hauke, Jan, Heitz, Florian ORCID: 0000-0002-2412-0352, Reuss, Alexander, Kommoss, Stefan, Marme, Frederik, Heimbach, Andre, Prieske, Katharina, Richters, Lisa, Burges, Alexander, Neidhardt, Guido, de Gregorio, Nikolaus, El-Balat, Ahmed, Hilpert, Felix, Meier, Werner, Kimmig, Rainer, Kast, Karin, Sehouli, Jalid, Baumann, Klaus, Jackisch, Christian, Park-Simon, Tjoung-Won, Hanker, Lars, Kroeber, Sandra, Pfisterer, Jacobus, Gevensleben, Heidrun, Schnelzer, Andreas, Dietrich, Dimo, Neunhoeffer, Tanja, Krockenberger, Mathias, Brucker, Sara Y., Nuernberg, Peter, Thiele, Holger, Altmueller, Janine, Lamla, Josefin, Elser, Gabriele, du Bois, Andreas, Hahnen, Eric and Schmutzler, Rita (2017). Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1). PLoS One, 12 (10). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Harter, Philipp, Hauke, Jan, Heitz, Florian, Reuss, Alexander, Kommoss, Stefan, Marme, Frederik, Heimbach, Andre, Prieske, Katharina, Richters, Lisa Katharina, Burges, Alexander, Neidhardt, Guido, de Gregorio, Nikolaus, El-Balat, Ahmed, Hilpert, Felix, Meier, Werner, Heubner, Martin Leonhard, Kast, Karin, Braicu, Ioana, Hahnen, Eric and Schmutzler, Rita K. (2016). Incidence of gernnline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1). J. Clin. Oncol., 34 (15). ALEXANDRIA: AMER SOC CLINICAL ONCOLOGY. ISSN 1527-7755

Hauke, Jan, Hahnen, Eric, Schneider, Stephanie, Reuss, Alexander, Richters, Lisa, Kommoss, Stefan, Heimbach, Andre, Marme, Frederik, Schmidt, Sandra, Prieske, Katharina, Gevensleben, Heidrun, Burges, Alexander, Borde, Julika, De Gregorio, Nikolaus, Nuernberg, Peter, El-Balat, Ahmed, Thiele, Holger, Hilpert, Felix, Altmueller, Janine, Meier, Werner, Dietrich, Dimo, Kimmig, Rainer, Schoemig-Markiefka, Birgid, Kast, Karin, Braicu, Elena, Baumann, Klaus, Jackisch, Christian, Park-Simon, Tjoung-Won, Ernst, Corinna, Hanker, Lars, Pfisterer, Jacobus, Schnelzer, Andreas, du Bois, Andreas, Schmutzler, Rita K. and Harter, Philipp (2019). Deleterious somatic variants in 473 consecutive individuals with ovarian cancer: results of the observational AGO-TR1 study (NCT02222883). J. Med. Genet., 56 (9). S. 574 - 581. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-6244

Knudsen, K., Krack, P., Tonder, L., Houeto, J. -L., Rau, J., Schade-Brittinger, C., Hartmann, A., Haelbig, Thomas D., Paschen, Stephen, Barbe, Michael T., Kuehn, Andrea, Fraix, Valerie, Brefel-Courbon, Christine, Vesper, Jan, Maltete, David, Sixel-Doering, Friederike, Weiss, Daniel, Witjas, Tatiana, Thobois, Stephane, Agid, Yves, Schnitzler, A., Schuepbach, W. M. M., Timmermann, L., Damier, Philippe, Vidailhet, M., Deuschl, G., Czernecki, Virginie, Hesekamp, Helke, Meier, Nildaus, Negovanska, Velina, Welter, Marie-Laure, Corvol, Jean-Christophe ORCID: 0000-0001-7325-0199, Pineau, Fanny, Cornu, Philippe, Navarro, Soledad, Paschen, Laura, Paschen, Stephen, Volkmann, Jens, Moeller, Bettina, Nebel, Adelheid, Witt, Karsten, Raethjen, Jan, Falk, Daniels, Mehdorn, Maktnilian, Meister, Ingo G., Kuhn, Jens, Dafsari, Haidar S., Fink, Gereon, Donner, Kerstin, Kessler, Josef, Maarouf, Mohammad, Kupsch, Andeas, Schneider, Gerd -H., Gruber, Doreen, Mueller, Bianca, Faust, Katharina, Chabardes, Stephan, Kistler, Andrea, Pollak, Pierre, Ory-Magne, Fabienne, Rascol, Oliver, Arbus, Christophe, Chaynes, P. Patrick, Danet, Lola, Derrey, Stephane, Lefaucheur, Romain, Benatru, Isabelle, Bataille, Benoit, Colin, Olivier, Wojtecki, Lars, Groiss, Stefan J., Elben, Saskia, Hartmann, Christian, Suedmeyer, Martin, Pinsker, Marcus O., Amtage, Florian, Gharabaghi, Alireza, Waechter, Tobias, Kruger, Rejko, Derkinderen, Pascal, Ledily, Severine, Raoul, Sylvia, Sauvaget, Anne, Elena-Klinik, Paracelsus, Trenkwalder, Claudia, Richter-Dreske, Wenke, Regis, Jean-Marie, Eusebio, Alexandro, Philippe, Jean, Polo, Gustavo, Pinto, Serge, Mertens, Patrick, Levin, Johannes ORCID: 0000-0001-5092-4306, Oertel, Wolfgang H., Dornier, Stephanie, Pene, Fredy, Hourton, Delphine, Bissery, Anne, Bouton, Didier, Quintin, Mathieu, Hoffart-Jourdain, Cecile, Brocvielle, Helene, Partowinia-Peters, Mahnaz, Schickor, Mandy, Balthasar, Kerstin, Stein, Meryem, Harnisch, Susanne, Reuss, Alexander, Aminossadati, Behnaz, Nasemann, Christian and Stoker, Valerie (2019). Programming parameters of subthalamic deep brain stimulators in Parkinson's disease from a controlled trial. Parkinsonism Relat. Disord., 65. S. 217 - 224. OXFORD: ELSEVIER SCI LTD. ISSN 1873-5126

Weber-Lassalle, Konstantin, Ernst, Corinna, Reuss, Alexander, Mollenhoff, Kathrin ORCID: 0000-0001-7861-3892, Baumann, Klaus, Jackisch, Christian, Hauke, Jan, Dietrich, Dimo, Borde, Julika, Park-Simon, Tjoung-Won, Hanker, Lars, Prieske, Katharina, Schmidt, Sandra, Weber-Lassalle, Nana, Pohl-Rescigno, Esther, Kommoss, Stefan, Marme, Frederik, Heitz, Florian, Stingl, Julia C., Schmutzler, Rita K., Harter, Philipp and Hahnen, Eric . Clonal Hematopoiesis-Associated Gene Mutations in a Clinical Cohort of 448 Patients With Ovarian Cancer. JNCI-J. Natl. Cancer Inst.. CARY: OXFORD UNIV PRESS INC. ISSN 1460-2105

Weber-Lassalle, Konstantin, Harter, Philipp, Hauke, Jan, Ernst, Corinna, Kommoss, Stefan, Marme, Frederik, Weber-Lassalle, Nana, Prieske, Katharina, Dietrich, Dimo, Borde, Julika, Pohl-Rescigno, Esther, Reuss, Alexander, Ataseven, Beyhan, Engel, Christoph ORCID: 0000-0002-7247-282X, Stingl, Julia C. ORCID: 0000-0002-1566-8156, Schmutzler, Rita K. and Hahnen, Eric (2018). Diagnosis of Li-Fraumeni Syndrome: Differentiating TP53 germline mutations from clonal hematopoiesis Results of the observational AGO-TR1 trial. Hum. Mutat., 39 (12). S. 2040 - 2047. HOBOKEN: WILEY. ISSN 1098-1004

This list was generated on Fri Mar 29 10:01:11 2024 CET.