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Signatures of mutational processes in human cancer., , , , , , , , , and 65 other author(s). Nature, 500 (7463): 415--421 (Aug 22, 2013)Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations., , , , , , , , , and 41 other author(s). Cell, 148 (1-2): 59--71 (January 2012)Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer., , , , , , , , , and 50 other author(s). Cancer Cell, 23 (2): 159--170 (February 2013)Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition., , , , , , , , , and 67 other author(s). Cancer Cell, 25 (3): 393--405 (March 2014)Dissecting the genomic complexity underlying medulloblastoma., , , , , , , , , and 80 other author(s). Nature, 488 (7409): 100--105 (August 2012)Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing., , , , , , , , , and 35 other author(s). Nature, 510 (7506): 537--541 (June 2014)Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma., , , , , , , , , and 66 other author(s). Nat Genet, 45 (8): 927--932 (August 2013)Hypermutation of the inactive X chromosome is a frequent event in cancer., , , , , , , , , and 26 other author(s). Cell, 155 (3): 567--581 (October 2013)Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma., , , , , , , , , and 69 other author(s). Nature, 511 (7510): 428--434 (July 2014)Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies., , , , , , , , , and 4 other author(s). PLoS One, 8 (6): e66621 (2013)