Jones, David T W

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Journal Article

Kolodziejczak, Anna S; Guerrini-Rousseau, Lea; Planchon, Julien Masliah; Ecker, Jonas; Selt, Florian; Mynarek, Martin; Obrecht, Denise; Sill, Martin; Autry, Robert J; Zhao, Eric; Hirsch, Steffen; Amouyal, Elsa; Dufour, Christelle; Ayrault, Olivier; Torrejon, Jacob; Waszak, Sebastian M; Ramaswamy, Vijay; Pentikainen, Virve; Demir, Haci Ahmet; Clifford, Steven C; ... (2023). Clinical outcome of pediatric medulloblastoma patients with Li-Fraumeni syndrome. Neuro-Oncology, 25(12), pp. 2273-2286. Oxford University Press 10.1093/neuonc/noad114

Kommoss, Felix K F; Stichel, Damian; Mora, Jaume; Esteller, Manel; Jones, David T W; Pfister, Stefan M; Brack, Eva; Wachtel, Marco; Bode, Peter Karl; Sinn, Hans-Peter; Schmidt, Dietmar; Mentzel, Thomas; Kommoss, Friedrich; Sahm, Felix; von Deimling, Andreas; Koelsche, Christian (2021). Clinicopathologic and molecular analysis of embryonal rhabdomyosarcoma of the genitourinary tract: evidence for a distinct DICER1-associated subgroup. Modern pathology, 34(8), pp. 1558-1569. Springer Nature 10.1038/s41379-021-00804-y

Waszak, Sebastian M; Robinson, Giles W; Gudenas, Brian L; Smith, Kyle S; Forget, Antoine; Kojic, Marija; Garcia-Lopez, Jesus; Hadley, Jennifer; Hamilton, Kayla V; Indersie, Emilie; Buchhalter, Ivo; Kerssemakers, Jules; Jäger, Natalie; Sharma, Tanvi; Rausch, Tobias; Kool, Marcel; Sturm, Dominik; Jones, David T W; Vasilyeva, Aksana; Tatevossian, Ruth G; ... (2020). Germline Elongator mutations in Sonic Hedgehog medulloblastoma. Nature, 580(7803), pp. 396-401. Macmillan Journals Ltd. 10.1038/s41586-020-2164-5

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; ... (2020). Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course. Acta neuropathologica, 139(1), pp. 193-209. Springer-Verlag 10.1007/s00401-019-02078-w

Reinhardt, Annekathrin; Stichel, Damian; Schrimpf, Daniel; Koelsche, Christian; Wefers, Annika K; Ebrahimi, Azadeh; Sievers, Philipp; Huang, Kristin; Casalini, M Belén; Fernández-Klett, Francisco; Suwala, Abigail; Weller, Michael; Gramatzki, Dorothee; Felsberg, Joerg; Reifenberger, Guido; Becker, Albert; Hans, Volkmar H; Prinz, Marco; Staszewski, Ori; Acker, Till; ... (2019). Tumors diagnosed as cerebellar glioblastoma comprise distinct molecular entities. Acta neuropathologica communications, 7(1), p. 163. BioMed Central 10.1186/s40478-019-0801-8

Reinhardt, Annekathrin; Stichel, Damian; Schrimpf, Daniel; Sahm, Felix; Korshunov, Andrey; Reuss, David E; Koelsche, Christian; Huang, Kristin; Wefers, Annika K; Hovestadt, Volker; Sill, Martin; Gramatzki, Dorothee; Felsberg, Joerg; Reifenberger, Guido; Koch, Arend; Thomale, Ulrich-W; Becker, Albert; Hans, Volkmar H; Prinz, Marco; Staszewski, Ori; ... (2018). Anaplastic astrocytoma with piloid features, a novel molecular class of IDH wildtype glioma with recurrent MAPK pathway, CDKN2A/B and ATRX alterations. Acta neuropathologica, 136(2), pp. 273-291. Springer 10.1007/s00401-018-1837-8

Waszak, Sebastian M; Northcott, Paul A; Buchhalter, Ivo; Robinson, Giles W; Sutter, Christian; Groebner, Susanne; Grund, Kerstin B; Brugières, Laurence; Jones, David T W; Pajtler, Kristian W; Morrissy, A Sorana; Kool, Marcel; Sturm, Dominik; Chavez, Lukas; Ernst, Aurelie; Brabetz, Sebastian; Hain, Michael; Zichner, Thomas; Segura-Wang, Maia; Weischenfeldt, Joachim; ... (2018). Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort. Lancet oncology, 19(6), pp. 785-798. Elsevier 10.1016/S1470-2045(18)30242-0

Sturm, Dominik; Orr, Brent A; Toprak, Umut H; Hovestadt, Volker; Jones, David T W; Capper, David; Sill, Martin; Buchhalter, Ivo; Northcott, Paul A; Leis, Irina; Ryzhova, Marina; Koelsche, Christian; Pfaff, Elke; Allen, Sariah J; Balasubramanian, Gnanaprakash; Worst, Barbara C; Pajtler, Kristian W; Brabetz, Sebastian; Johann, Pascal D; Sahm, Felix; ... (2016). New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs. Cell, 164(5), pp. 1060-1072. Cell Press 10.1016/j.cell.2016.01.015

Pajtler, Kristian W; Witt, Hendrik; Sill, Martin; Jones, David T W; Hovestadt, Volker; Kratochwil, Fabian; Wani, Khalida; Tatevossian, Ruth; Punchihewa, Chandanamali; Johann, Pascal; Reimand, Jüri; Warnatz, Hans-Jörg; Ryzhova, Marina; Mack, Steve; Ramaswamy, Vijay; Capper, David; Schweizer, Leonille; Sieber, Laura; Wittmann, Andrea; Huang, Zhiqin; ... (2015). Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups. Cancer cell, 27(5), pp. 728-743. Cell Press 10.1016/j.ccell.2015.04.002

Koelsche, Christian; Hovestadt, Volker; Jones, David T W; Capper, David; Sturm, Dominik; Sahm, Felix; Schrimpf, Daniel; Adeberg, Sebastian; Böhmer, Katja; Hagenlocher, Christian; Mechtersheimer, Gunhild; Kohlhof, Patricia; Mühleisen, Helmut; Beschorner, Rudi; Hartmann, Christian; Braczynski, Anne Kristin; Mittelbronn, Michel; Buslei, Rolf; Becker, Albert; Grote, Alexander; ... (2015). Melanotic tumors of the nervous system are characterized by distinct mutational, chromosomal and epigenomic profiles. Brain pathology, 25(2), pp. 202-208. Blackwell 10.1111/bpa.12228

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