Dermot P B Mcgovern

Ontology type: schema:Person     

Person Info


Dermot P B



Publications in SciGraph latest 50 shown

  • 2019 Semantic Segmentation of Colon Glands in Inflammatory Bowel Disease Biopsies in INFORMATION TECHNOLOGY IN BIOMEDICINE
  • 2016-11-25 Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease in NATURE COMMUNICATIONS
  • 2016-08-09 A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis in NATURE COMMUNICATIONS
  • 2016-08 Analysis of protein-coding genetic variation in 60,706 humans in NATURE
  • 2015-02 High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis in NATURE GENETICS
  • 2014-11 Reprograming of gut microbiome energy metabolism by the FUT2 Crohn’s disease risk polymorphism in THE ISME JOURNAL
  • 2014-10 The role of glycosylation in IBD in NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY
  • 2014-09 A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia in NATURE GENETICS
  • 2014-09 Use of animal models in elucidating disease pathogenesis in IBD in SEMINARS IN IMMUNOPATHOLOGY
  • 2014-05 Towards personalized care in IBD in NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY
  • 2013-05 Assessing Health Status in Inflammatory Bowel Disease Using a Novel Single-Item Numeric Rating Scale in DIGESTIVE DISEASES AND SCIENCES
  • 2009-12 Common variants at five new loci associated with early-onset inflammatory bowel disease in NATURE GENETICS
  • 2009-10 Susceptibility to Crohn’s disease is mediated by KIR2DL2/KIR2DL3 heterozygosity and the HLA-C ligand in IMMUNOGENETICS
  • 2009-09 Phenotypic and Genotypic Characteristics of Inflammatory Bowel Disease in French Canadians: Comparison With a Large North American Repository in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2009-02 Ulcerative colitis–risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study in NATURE GENETICS
  • 2005-04 A common CTLA4 haplotype associated with coeliac disease in EUROPEAN JOURNAL OF HUMAN GENETICS
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