Andrew J Mungall


Ontology type: schema:Person     


Person Info

NAME

Andrew J

SURNAME

Mungall

Publications in SciGraph latest 50 shown

  • 2018-12 Whole genome and whole transcriptome genomic profiling of a metastatic eccrine porocarcinoma in NPJ PRECISION ONCOLOGY
  • 2018-10 The genetic basis and cell of origin of mixed phenotype acute leukaemia in NATURE
  • 2018-04 Erratum: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions in NATURE MEDICINE
  • 2018-01 The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions in NATURE MEDICINE
  • 2017-12 Increasing quality, throughput and speed of sample preparation for strand-specific messenger RNA sequencing in BMC GENOMICS
  • 2017-12 The North American bullfrog draft genome provides insight into hormonal regulation of long noncoding RNA in NATURE COMMUNICATIONS
  • 2017-10 A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor in NATURE GENETICS
  • 2017-09 Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy in NATURE
  • 2017-07 The whole-genome landscape of medulloblastoma subtypes in NATURE
  • 2017-06 Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes in NATURE GENETICS
  • 2017-05 Spatial heterogeneity in medulloblastoma in NATURE GENETICS
  • 2016-11-08 Genomic analyses identify recurrent MEF2D fusions in acute lymphoblastic leukaemia in NATURE COMMUNICATIONS
  • 2016-07 Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer in NATURE GENETICS
  • 2016-07 A somatic reference standard for cancer genome sequencing in SCIENTIFIC REPORTS
  • 2016-04 Validation and calibration of next-generation sequencing to identify Epstein-Barr virus-positive gastric cancer in The Cancer Genome Atlas in GASTRIC CANCER
  • 2016-01 Divergent clonal selection dominates medulloblastoma at recurrence in NATURE
  • 2015-12 Immunogenicity of recurrent mutations in MYD88 and EZH2 in non-Hodgkin lymphomas in JOURNAL FOR IMMUNOTHERAPY OF CANCER
  • 2015-12 Epigenetic and transcriptional determinants of the human breast in NATURE COMMUNICATIONS
  • 2015-12 MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours in NATURE COMMUNICATIONS
  • 2015-12 Comprehensive miRNA sequence analysis reveals survival differences in diffuse large B-cell lymphoma patients in GENOME BIOLOGY
  • 2015-12 The genomic and transcriptomic landscape of anaplastic thyroid cancer: implications for therapy in BMC CANCER
  • 2015-02 Integrative analysis of 111 reference human epigenomes in NATURE
  • 2015-02 Dynamics of genomic clones in breast cancer patient xenografts at single-cell resolution in NATURE
  • 2014-07-09 Comprehensive molecular profiling of lung adenocarcinoma in NATURE
  • 2013-12 Barnacle: detecting and characterizing tandem duplications and fusions in transcriptome assemblies in BMC GENOMICS
  • 2013-07 DNA hypomethylation within specific transposable element families associates with tissue-specific enhancer landscape in NATURE GENETICS
  • 2013-05-01 Integrated genomic characterization of endometrial carcinoma in NATURE
  • 2012-09-23 Comprehensive molecular portraits of human breast tumours in NATURE
  • 2012-08 Subgroup-specific structural variation across 1,000 medulloblastoma genomes in NATURE
  • 2011-08 Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma in NATURE
  • 2010-02 Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin in NATURE GENETICS
  • 2008-08 Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians in NATURE GENETICS
  • 2007-12 The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals in BMC EVOLUTIONARY BIOLOGY
  • 2007-02 RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer in ONCOGENE
  • 2006-02 Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH in ONCOGENE
  • 2003-10 The DNA sequence and analysis of human chromosome 6 in NATURE
  • 2003-07 β-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation in MOLECULAR PSYCHIATRY
  • 2002-12 The human homologue of unc-93 maps to chromosome 6q27 – characterisation and analysis in sporadic epithelial ovarian cancer in BMC GENETICS
  • 2002-10 Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors in ONCOGENE
  • 2002-01 Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer in ONCOGENE
  • 2001-05 Vanin genes are clustered (human 6q22–24 and mouse 10A2B1) and encode isoforms of pantetheinase ectoenzymes in IMMUNOGENETICS
  • 2001-02 Comparison of human genetic and sequence-based physical maps in NATURE
  • 2001-02 The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X in NATURE
  • 2001-02 Initial sequencing and analysis of the human genome in NATURE
  • 1998-10 Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy in NATURE GENETICS
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