Rezultati pretrage - Daniel W. Fults

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    TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma od Marc Remke, Vijay Ramaswamy, John Peacock, David Shih, Christian Koelsche, Paul A. Northcott, Nadia Hill, Florence M.G. Cavalli, Marcel Kool, Xin Wang, Stephen C. Mack, Mark Barszczyk, A. Sorana Morrissy, Xiaochong Wu, Sameer Agnihotri, Betty Luu, David Jones, Livia Garzia, Adrian M. Dubuc, Nataliya Zhukova, Robert J. Vanner, Johan M. Kros, Pim J. French, Erwin G. Van Meir, Rajeev Vibhakar, Karel Zitterbart, Jennifer A. Chan, László Bognár, Álmos Klekner, Bolesław Lach, Shin Jung, Ali G. Saad, Linda M. Liau, Steffen Albrecht, Massimo Zollo, Michael K. Cooper, Reid C. Thompson, Olivier Delattre, Franck Bourdeaut, François Doz, Miklós Garami, Péter Hauser, Carlos Gilberto Carlotti, Timothy Van Meter, Luca Massimi, Daniel W. Fults, Scott L. Pomeroy, Toshiro Kumabe, Young Shin, Jeffrey R. Leonard, Samer K. Elbabaa, Jaume Mora, Joshua B. Rubin, Yoon‐Jae Cho, Roger E. McLendon, Darell D. Bigner, Charles G. Eberhart, Maryam Fouladi, Robert J. Wechsler‐Reya, Cláudia C. Faria, Sidney Croul, Annie Huang, Éric Bouffet, Cynthia Hawkins, Peter B. Dirks, William A. Weiss, Ulrich Schüller, Ian F. Pollack, Stefan Rutkowski, David Meyronet, Anne Jouvet, Michelle Fèvre‐Montange, Nada Jabado, Marta Perek‐Polnik, Wiesława Grajkowska, Seung-Ki Kim, James T. Rutka, David Malkin, Uri Tabori, Stefan M. Pfister, Andrey Korshunov, Andreas von Deimling, Michael D. Taylor

    Izdano 2013
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  11. 11

    Epigenomic alterations define lethal CIMP-positive ependymomas of infancy od Stephen C. Mack, Hendrik Witt, Rosario M. Piro, Lei Gu, Scott Zuyderduyn, Adrian M. Stütz, Xin Wang, Marco Gallo, Livia Garzia, Kory Zayne, Xiaoyang Zhang, Vijay Ramaswamy, Natalie Jäger, David Jones, Martin Sill, Trevor J. Pugh, Marina Ryzhova, Khalida Wani, David Shih, Renee Head, Marc Remke, Swneke D. Bailey, Thomas Zichner, Cláudia C. Faria, Mark Barszczyk, Sebastian Stark, Huriye Seker‐Cin, Sonja Hutter, Pascal D. Johann, Sebastian Bender, Volker Hovestadt, Theophilos Tzaridis, Adrian M. Dubuc, Paul A. Northcott, J.H. Peacock, Kelsey C. Bertrand, Sameer Agnihotri, Florence M.G. Cavalli, Ian D. Clarke, Kathleen Nethery-Brokx, Caretha L. Creasy, Sharad K. Verma, Jan Köster, Xiangji Wu, Yuan Yao, Till Milde, Patrick Sin‐Chan, Jennifer Zuccaro, Lynette Lau, Sérgio L. Pereira, Pedro Castelo‐Branco, Martin Hirst, Marco A. Marra, Stephen S. Roberts, Daniel W. Fults, Luca Massimi, Y. J. Cho, Timothy Van Meter, Wiesława Grajkowska, Bolesław Lach, Andreas E. Kulozik, Andreas von Deimling, Olaf Witt, Stephen W. Scherer, Xing Fan, Karin M. Muraszko, Marcel Kool, Scott L. Pomeroy, Nalin Gupta, Joanna J. Phillips, Annie Huang, Uri Tabori, Cynthia Hawkins, David Malkin, Paul Kongkham, William A. Weiss, Nada Jabado, James T. Rutka, Éric Bouffet, Jan O. Korbel, Mathieu Lupien, Kenneth Aldape, Gary D. Bader, Roland Eils, Peter Lichter, Peter B. Dirks, Stefan M. Pfister, Andrey Korshunov, Michael D. Taylor

    Izdano 2014
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  12. 12

    Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort od Sebastian M. Waszak, Paul A. Northcott, Ivo Buchhalter, Giles Robinson, Christian Sutter, Susanne N. Groebner, Kerstin Grund, Laurence Brugières, David Jones, Kristian W. Pajtler, A. Sorana Morrissy, Marcel Kool, Dominik Sturm, Lukas Chávez, Aurélie Ernst, Sebastian Brabetz, M. Hain, Thomas Zichner, Maia Segura‐Wang, Joachim Weischenfeldt, Tobias Rausch, Balca R. Mardin, Xin Zhou, Cristina Baciu, Christian Lawerenz, Jennifer A. Chan, Pascale Varlet, Léa Guerrini‐Rousseau, Daniel W. Fults, Wiesława Grajkowska, Péter Hauser, Nada Jabado, Young‐Shin Ra, Karel Zitterbart, Suyash Shringarpure, Francisco M. De La Vega, Carlos D. Bustamante, Ho‐Keung Ng, Arie Perry, Tobey J. MacDonald, Pablo Hernáiz Driever, Anne Bendel, Daniel C. Bowers, Geoffrey McCowage, Murali Chintagumpala, Richard J. Cohn, Tim Hassall, Gudrun Fleischhack, Tone Eggen, Finn Wesenberg, Maria Feychting, Birgitta Lannering, Joachim Schüz, Christoffer Johansen, Tina Veje Andersen, Martin Röösli, Claudia E. Kuehni, Michael Grotzer, Kristina Kjærheim, Camelia M. Monoranu, Tenley C. Archer, Elizabeth S. Duke, Scott L. Pomeroy, Shelagh Redmond, Stephan Frank, David Sumerauer, Wolfram Scheurlen, Marina Ryzhova, Till Milde, Christian P. Kratz, David Samuel, Jinghui Zhang, David A. Solomon, Marco A. Marra, Roland Eils, Claus R. Bartram, Katja von Hoff, Stefan Rutkowski, Vijay Ramaswamy, Richard J. Gilbertson, Andrey Korshunov, Michael D. Taylor, Peter Lichter, David Malkin, Amar Gajjar, Jan O. Korbel, Stefan M. Pfister

    Izdano 2018
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  13. 13

    Divergent clonal selection dominates medulloblastoma at recurrence od A. Sorana Morrissy, Livia Garzia, David Shih, Scott Zuyderduyn, Xi Huang, Patryk Skowron, Marc Remke, Florence M.G. Cavalli, Vijay Ramaswamy, Patricia Lindsay, Salomeh Jelveh, Laura Donovan, Xin Wang, Betty Luu, Kory Zayne, Yisu Li, Chelsea Mayoh, Nina Thiessen, Eloi Mercier, Karen Mungall, Yusanne Ma, Kane Tse, Thomas Zeng, Karey Shumansky, Andrew Roth, Sohrab P. Shah, Hamza Farooq, Noriyuki Kijima, Borja Holgado, John J. Y. Lee, Stuart Matan-Lithwick, Jessica Liu, Stephen C. Mack, Alex Manno, Kulandaimanuvel Antony Michealraj, Carolina Nör, John Peacock, Lei Qin, Jüri Reimand, Adi Rolider, Yuan Thompson, Xiaochong Wu, Trevor J. Pugh, Adrian Ally, Mikhail Bilenky, Yaron S.N. Butterfield, Rebecca Carlsen, Young Cheng, Eric Chuah, Richard Corbett, Noreen Dhalla, Anyuan He, Darlene Lee, Haiyan I. Li, William D. Long, Michael Mayo, Patrick Plettner, Jenny Q. Qian, Jacqueline E. Schein, Angela Tam, Tina Wong, İnanç Birol, Yongjun Zhao, Cláudia C. Faria, José Pimentel, Sofía Nunes, Tarek Shalaby, Michael Grotzer, Ian F. Pollack, Ronald L. Hamilton, Xiao‐Nan Li, Anne Bendel, Daniel W. Fults, Andrew W. Walter, Toshihiro Kumabe, Teiji Tominaga, V. Peter Collins, Yoon-Jae Cho, Caitlin Hoffman, David Lyden, Jeffrey H. Wisoff, James H. Garvin, Duncan Stearns, Luca Massimi, Ulrich Schüller, Jaroslav Štěrba, Karel Zitterbart, Stéphanie Puget, Olivier Ayrault, Sandra E. Dunn, Daniela Pretti da Cunha Tirapelli, Carlos Gilberto Carlotti, Helen Wheeler, Andrew R. Hallahan, Wendy J. Ingram, Tobey J. MacDonald, Jeffrey J. Olson, Erwin G. Van Meir, Ji-Yeoun Lee, Kyu‐Chang Wang

    Izdano 2016
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  14. 14

    Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors od Jonathon Torchia, Brian Golbourn, Shengrui Feng, King Ching Ho, Patrick Sin‐Chan, Alexandre Vasiljevic, Joseph Norman, Paul Guilhamon, Livia Garzia, Natalia R. Agamez, Mei Lu, Tiffany Sin Yu Chan, Daniel Picard, Pasqualino de Antonellis, Dong-Anh Khuong-Quang, Aline Cristiane Planello, Constanze Zeller, Dalia Baršytė-Lovejoy, Lucie Lafay‐Cousin, Louis Létourneau, Mathieu Bourgey, Man Yu, Deena M.A. Gendoo, Misko Dzamba, Mark Barszczyk, Tiago da Silva Medina, Alexandra N. Riemenschneider, A. Sorana Morrissy, Young‐Shin Ra, Vijay Ramaswamy, Marc Remke, Christopher Dunham, Stephen Yip, Ho‐Keung Ng, Jian‐Qiang Lu, Vivek Mehta, Steffen Albrecht, José Pimentel, Jennifer A. Chan, Gino R. Somers, Cláudia C. Faria, Lúcia Roque, Maryam Fouladi, Lindsey M. Hoffman, Andrew S. Moore, Yin Wang, Seung Ah Choi, Jordan R. Hansford, Daniel Catchpoole, Diane K. Birks, Nicholas K. Foreman, Doug Strother, Álmos Klekner, László Bognár, Miklós Garami, Péter Hauser, Tibor Hortobágyi, Beverly Wilson, Juliette Hukin, Anne-Sophie Carret, Timothy Van Meter, Eugene Hwang, Amar Gajjar, Shih‐Hwa Chiou, Hideo Nakamura, Helen Toledano, Iris Fried, Daniel W. Fults, Takafumi Wataya, Chris Fryer, David D. Eisenstat, Katrin Scheinemann, Adam Fleming, Donna L. Johnston, Jean Michaud, Shayna Zelcer, Robert Hammond, Samina Afzal, David A. Ramsay, Nongnuch Sirachainan, Suradej Hongeng, Noppadol Larbcharoensub, Richard G. Grundy, Rishi Lulla, Jason Fangusaro, Harriet Druker, Ute Bartels, Ronald Grant, David Malkin, C. Jane McGlade, Theodore Nicolaides, Tarık Tihan, Joanna J. Phillips, Jacek Majewski, Alexandre Montpetit, Guillaume Bourque, Gary D. Bader, Alyssa Reddy, G. Yancey Gillespie, Monika Warmuth‐Metz

    Izdano 2016
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