| Data | Título | Autor(es) | Tipo | Acesso |
| 27-Jan-2021 | Clinical outcomes and patient-matched molecular composition of relapsed medulloblastoma | Kumar, Rahul; Smith, Kyle S.; Deng, Maximilian; Terhune, Colt; Robinson, Giles W; Orr, Brent A.; Liu, Anthony P. Y.; Lin, Tong; Billups, Catherine A.; Chintagumpala, Murali; Bowers, Daniel C.; Hassall, Timothy E.; Hansford, Jordan R.; Khuong-Quang, Dong Anh; Crawford, John R.; Bendel, Anne E.; Gururangan, Sridharan; Schroeder, Kristin; Bouffet, Eric; Bartels, Ute; Fisher, Michael J.; Cohn, Richard; Partap, Sonia; Kellie, Stewart J.; McCowage, Geoffrey; Paulino, Arnold C.; Rutkowski, Stefan; Fleischhack, Gudrun; Dhall, Girish; Klesse, Laura J.; Leary, Sarah; Nazarian, Javad; Kool, Marcel; Wesseling, Pieter; Ryzhova, Marina; Zheludkova, Olga; Golanov, Andrey V.; McLendon, Roger E.; Packer, Roger J.; Dunham, Christopher; Hukin, Juliette; Fouladi, Maryam; Faria, Claudia; Pimentel, José; Walter, Andrew W.; Jabado, Nada; Cho, Yoon-Jae; Perreault, Sebastien; Croul, Sidney E.; Zapotocky, Michal; Hawkins, Cynthia; Tabori, Uri; Taylor, Michael D.; Pfister, Stefan M.; Klimo, Paul; Boop, Frederick A.; Ellison, David W.; Merchant, Thomas E.; Onar-Thomas, Arzu; Korshunov, Andrey; Jones, David T. W.; Gajjar, Amar; Ramaswamy, Vijay; Northcott, Paul A. | article |  |
| 2019 | Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course | Wefers, Annika K.; Stichel, Damian; Schrimpf, Daniel; Coras, Roland; Pages, Mélanie; Tauziède-Espariat, Arnault; Varlet, Pascale; Schwarz, Daniel; Söylemezoglu, Figen; Pohl, Ute; Pimentel, José; Meyer, Jochen; Hewer, Ekkehard; Japp, Anna; Joshi, Abhijit; Reuss, David E.; Reinhardt, Annekathrin; Sievers, Philipp; Casalini, M. Belén; Ebrahimi, Azadeh; Huang, Kristin; Koelsche, Christian; Low, Hu Liang; Rebelo, Olinda; Marnoto, Dina; Becker, Albert J.; Staszewski, Ori; Mittelbronn, Michel; Hasselblatt, Martin; Schittenhelm, Jens; Cheesman, Edmund; de Oliveira, Ricardo Santos; Queiroz, Rosane Gomes P.; Valera, Elvis Terci; Hans, Volkmar H.; Korshunov, Andrey; Olar, Adriana; Ligon, Keith L.; Pfister, Stefan M.; Jaunmuktane, Zane; Brandner, Sebastian; Tatevossian, Ruth G.; Ellison, David W.; Jacques, Thomas S.; Honavar, Mrinalini; Aronica, Eleonora; Thom, Maria; Sahm, Felix; von Deimling, Andreas; Jones, David T. W.; Blumcke, Ingmar; Capper, David | article |  |
| 2019 | Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma | Suzuki, Hiromichi; Kumar, Sachin A.; Shuai, Shimin; Diaz-Navarro, Ander; Gutierrez-Fernandez, Ana; De Antonellis, Pasqualino; Cavalli, Florence M. G.; Juraschka, Kyle; Farooq, Hamza; Shibahara, Ichiyo; Vladoiu, Maria C.; Zhang, Jiao; Abeysundara, Namal; Przelicki, David; Skowron, Patryk; Gauer, Nicole; Luu, Betty; Daniels, Craig; Wu, Xiaochong; Forget, Antoine; Momin, Ali; Wang, Jun; Dong, Weifan; Kim, Seung-Ki; Grajkowska, Wieslawa A.; Jouvet, Anne; Fèvre-Montange, Michelle; Garrè, Maria Luisa; Nageswara Rao, Amulya A.; Giannini, Caterina; Kros, Johan M; French, Pim J.; Jabado, Nada; Ng, Ho-Keung; Poon, Wai Sang; Eberhart, Charles G.; Pollack, Ian F.; Olson, James M.; Weiss, William A.; Kumabe, Toshihiro; López-Aguilar, Enrique; Lach, Boleslaw; Massimino, Maura; Van Meir, Erwin G.; Rubin, Joshua B.; Vibhakar, Rajeev; Chambless, Lola B.; Kijima, Noriyuki; Klekner, Almos; Bognár, László; Chan, Jennifer A.; Faria, Claudia; Ragoussis, Jiannis; Pfister, Stefan M.; Goldenberg, Anna; Wechsler-Reya, Robert J.; Bailey, Swneke D.; Garzia, Livia; Morrissy, A Sorana; Marra, Marco A.; Huang, Xi; Malkin, David; Ayrault, Olivier; Ramaswamy, Vijay; Puente, Xose S.; Calarco, John A.; Stein, Lincoln; Taylor, Michael D. | article | |
