Kool, Marcel
German Cancer Research Center · Hopp Children's Cancer Center Heidelberg
27 papers on CoChatORCID 0000-0002-6557-5468
Most cited papers
- Verified
TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma
Remke, M., Ramaswamy, V., Peacock, J., Shih, D. J. H., Koelsche, C., Northcott, P. A., Hill, N., Cavalli, F. M. G., Kool, M., Wang, X., et al. (2013) · Acta Neuropathologica
Glioma Diagnosis and TreatmentCancer Genomics and Diagnostics
Cited by 164
- Verified
Hypermutation of the Inactive X Chromosome Is a Frequent Event in Cancer
Jäger, N., Schlesner, M., Jones, D. T. W., Raffel, S., Mallm, J.-P., Junge, K. M., Weichenhan, D., Bauer, T., Ishaque, N., Kool, M., et al. (2013) · Cell
Cancer Genomics and DiagnosticsChromatin Remodeling and Cancer
Cited by 90
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The Senescence-associated Secretory Phenotype Mediates Oncogene-induced Senescence in Pediatric Pilocytic Astrocytoma
Buhl, J. L., Selt, F., Hielscher, T., Guiho, R., Ecker, J., Sahm, F., Ridinger, J., Riehl, D., Usta, D., Ismer, B., et al. (2019) · Clinical Cancer Research
Telomeres, Telomerase, and SenescenceGlioma Diagnosis and Treatment
Cited by 84
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