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Intertumoral Heterogeneity within Medulloblastoma Subgroups.
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Subtypes of medulloblastoma have distinct developmental origins.
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The whole-genome landscape of medulloblastoma subtypes.
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Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma.
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Medulloblastoma can be initiated by deletion of Patched in lineage-restricted progenitors or stem cells.
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Dissecting the genomic complexity underlying medulloblastoma.
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Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition.
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Combined MYC and P53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease.
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Integrated genomics identifies five medulloblastoma subtypes with distinct genetic profiles, pathway signatures and clinicopathological features.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.