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Acta Neuropathologica|November 28, 2012
Aberrant patterns of H3K4 and H3K27 histone lysine methylation occur across subgroups in medulloblastomaAdrian M Dubuc, Marc Remke, Andrey Korshunov, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Lessons learned from the application of whole-genome analysis to the treatment of patients with advanced cancersJanessa Laskin, Steven Jones, Samuel Aparicio, et al.
Cancer Cell|September 13, 2017
Identification of GPC2 as an Oncoprotein and Candidate Immunotherapeutic Target in High-Risk NeuroblastomaKristopher R Bosse, Pichai Raman, Zhongyu Zhu, et al.
Nature|March 4, 2011
MHC class II transactivator CIITA is a recurrent gene fusion partner in lymphoid cancersChristian Steidl, Sohrab P Shah, Bruce W Woolcock, et al.
Genome Research|February 14, 2004
Development and application of a salmonid EST database and cDNA microarray: data mining and interspecific hybridization characteristicsMatthew L Rise, Kristian R von Schalburg, Gordon D Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1Tali Mazor, Charles Chesnelong, Aleksandr Pankov, et al.
Blood Advances|June 27, 2020
Genetic and evolutionary patterns of treatment resistance in relapsed B-cell lymphomaChristopher K Rushton, Sarah E Arthur, Miguel Alcaide, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 5, 2020
Uncovering Clinically Relevant Gene Fusions with Integrated Genomic and Transcriptomic Profiling of Metastatic CancersErica S Tsang, Cameron J Grisdale, Erin Pleasance, et al.
Cancer Cell|June 24, 2014
Quiescent sox2(+) cells drive hierarchical growth and relapse in sonic hedgehog subgroup medulloblastomaRobert J Vanner, Marc Remke, Marco Gallo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2020
Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencingMy Linh Thibodeau, Kieran O'Neill, Katherine Dixon, et al.
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