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Showing 1–12 of 12 results
Advanced filters: Author: "Peter Lichter" Clear advanced filters
  • Viral pathogen load in cancer genomes is estimated through analysis of sequencing data from 2,656 tumors across 35 cancer types using multiple pathogen-detection pipelines, identifying viruses in 382 genomic and 68 transcriptome datasets.

    • Marc Zapatka
    • Ivan Borozan
    • Christian von Mering
    ResearchOpen Access
    Nature Genetics
    Volume: 52, P: 320-330
  • Genomic analysis of 491 medulloblastoma samples, including methylation profiling of 1,256 cases, effectively assigns candidate drivers to most tumours across all molecular subgroups.

    • Paul A. Northcott
    • Ivo Buchhalter
    • Peter Lichter
    ResearchOpen Access
    Nature
    Volume: 547, P: 311-317
  • There is an increasing realization of epigenetic dysregulation in cancer, which comprises both the mutation of genes encoding epigenetic regulators and the broader disruptions to chromatin states of the epigenome. This Review discusses our latest understanding of these phenomena, their convergence and the implications for cancer biology and therapeutics.

    • Christoph Plass
    • Stefan M. Pfister
    • Peter Lichter
    Reviews
    Nature Reviews Genetics
    Volume: 14, P: 765-780
  • The latest large-scale genomic and epigenomic profiling studies have yielded an unprecedented abundance of novel data and provided deeper insights into gliomagenesis across all age groups. These studies have highlighted key distinctions, but also some commonalities, which are discussed in this Review.

    • Dominik Sturm
    • Sebastian Bender
    • Stefan M. Pfister
    Reviews
    Nature Reviews Cancer
    Volume: 14, P: 92-107
  • Medulloblastoma has been the subject of numerous genomics and transcriptomics studies that have led to this disease being subclassified into various clinically meaningful groups and to advances in understanding the biology of these subgroups, with implications for treatment.

    • Paul A. Northcott
    • David T. W. Jones
    • Stefan M. Pfister
    Reviews
    Nature Reviews Cancer
    Volume: 12, P: 818-834
  • Medulloblastoma is a malignant childhood brain tumour presenting major clinical challenges; here, a comprehensive genome-wide DNA methylation data set from human and mouse tumours, coupled with analysis of histone modifications, RNA transcripts and genome sequencing, uncovers a wealth of alterations that provide insights into the epigenetic regulation of transcription and genome organization in medulloblastoma pathogenesis.

    • Volker Hovestadt
    • David T. W. Jones
    • Peter Lichter
    Research
    Nature
    Volume: 510, P: 537-541
  • Precision medicine has dramatically changed the landscape of drug development in oncology, but this paradigm shift remains to be adopted in early phase clinical trials of molecularly targeted agents and immunotherapeutic agents in children with cancer. The authors, members of the Innovative Therapies for Children with Cancer (ITCC) Consortium, describe trial design strategies to enable drugs with promising activity to progress rapidly to randomized studies and, therefore, substantially accelerate drug development for children and adolescents with cancer.

    • Lucas Moreno
    • Andrew D. J. Pearson
    • Gilles Vassal
    Reviews
    Nature Reviews Clinical Oncology
    Volume: 14, P: 497-507
  • Medulloblastoma, once thought to represent a single disease entity, is now recognized to comprise distinct subgroups that can be identified using histological, genetic and transcriptomic approaches. Northcott et al. present the evidence for the four recently defined subgroups of medulloblastoma, and highlight how stratification of tumours into these subgroups could have important clinical implications for patient prognosis, treatment and care.

    • Paul A. Northcott
    • Andrey Korshunov
    • Michael D. Taylor
    Reviews
    Nature Reviews Neurology
    Volume: 8, P: 340-351
  • Many factors, including genetic and epigenetic alterations, antigenic drive and the microenvironment, are crucial in the initiation and progression of chronic lymphocytic leukaemia (CLL). How will our growing understanding of CLL biology lead to the translation of therapeutic targets and prognostic markers into clinical practice?

    • Thorsten Zenz
    • Daniel Mertens
    • Stephan Stilgenbauer
    Reviews
    Nature Reviews Cancer
    Volume: 10, P: 37-50