Mark T Ross

Ontology type: schema:Person     

Person Info


Mark T



Publications in SciGraph latest 50 shown

  • 2018-10 Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project in GENETICS IN MEDICINE
  • 2016-05-10 The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes in NATURE COMMUNICATIONS
  • 2015-09 Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma in NATURE GENETICS
  • 2014-10 Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics in GENOME MEDICINE
  • 2014-02 Intraclonal heterogeneity is a critical early event in the development of myeloma and precedes the development of clinical symptoms in LEUKEMIA
  • 2013-12 Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2 in NATURE COMMUNICATIONS
  • 2012-07 BAP1 loss defines a new class of renal cell carcinoma in NATURE GENETICS
  • 2010-01 A comprehensive catalogue of somatic mutations from a human cancer genome in NATURE
  • 2008-11 Accurate whole human genome sequencing using reversible terminator chemistry in NATURE
  • 2007-02 Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials in CHROMOSOME RESEARCH
  • 2005-10 Isolation, X location and activity of the marsupial homologue of SLC16A2, an XIST-flanking gene in eutherian mammals in CHROMOSOME RESEARCH
  • 2003-06 Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma in NATURE GENETICS
  • 2003-03 Construction and integration of radiation-hybrid and cytogenetic maps of dog Chromosome X in MAMMALIAN GENOME
  • 2001-06 Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region in HUMAN GENETICS
  • 1998-09 UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1998-05 Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2) in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1996-10 A radiation hybrid map spanning the entire human X Chromosome integrating YACs, genes, and STS markers in MAMMALIAN GENOME
  • 1992-07 Selection of a human chromosome 21 enriched YAC sub–library using a chromosome–specific composite probe in NATURE GENETICS
  • 1992-06 Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region in NATURE GENETICS
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