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Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies., , , , , , , , , and 4 other author(s). PLoS One, 8 (6): e66621 (2013)Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia, , , , , , , , , and 19 other author(s). PLoS Genet, 10 (6): e1004345 (June 2014)scSNPdemux: a sensitive demultiplexing pipeline using single nucleotide polymorphisms for improved pooled single-cell RNA sequencing analysis., , , , , , and . BMC Bioinform., 24 (1): 326 (December 2023)Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma., , , , , , , , , and 66 other author(s). Nat Genet, 45 (8): 927--932 (August 2013)Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma., , , , , , , , , and 69 other author(s). Nature, 511 (7510): 428--434 (July 2014)Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia., , , , , , , , , and 19 other author(s). PLoS Genet, 10 (6): e1004345 (June 2014)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)Oligonucleotide array-based comparative genomic hybridization (aCGH) of 90 neuroblastomas reveals aberration patterns closely associated with relapse pattern and outcome., , , , , , , , , and . Genes Chromosomes Cancer, 45 (12): 1130--1142 (December 2006)Conumee 2.0: enhanced copy-number variation analysis from DNA methylation arrays for humans and mice., , , , , , , , , and 1 other author(s). Bioinform., (February 2024)Active medulloblastoma enhancers reveal subgroup-specific cellular origins., , , , , , , , , and 29 other author(s). Nat., 530 (7588): 57-62 (2016)