Philippe Goyette


Ontology type: schema:Person     


Person Info

NAME

Philippe

SURNAME

Goyette

Publications in SciGraph latest 50 shown

  • 2017-06-14 Genetic loci associated with heart rate variability and their effects on cardiac disease risk in NATURE COMMUNICATIONS
  • 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
  • 2013-06 Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
  • 2012-11 Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease in NATURE
  • 2011-11 Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease in NATURE GENETICS
  • 2011-01 A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles in GENES & IMMUNITY
  • 2010-11 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index in NATURE GENETICS
  • 2010-04 Genome-wide association identifies multiple ulcerative colitis susceptibility loci in NATURE GENETICS
  • 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
  • 2008-10 MAST3: a novel IBD risk factor that modulates TLR4 signaling in GENES & IMMUNITY
  • 2008-09 Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease in NATURE GENETICS
  • 2008-03 Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis in MUCOSAL IMMUNOLOGY
  • 2007-05 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis in NATURE GENETICS
  • 2002-09 Multiple transcription start sites and alternative splicing in the methylenetetrahydrofolate reductase gene result in two enzyme isoforms in MAMMALIAN GENOME
  • 1998-08 Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1998-08 Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR) in MAMMALIAN GENOME
  • 1996-04 NEW MUTATION IDENTIFIED IN FOUR UNRELATED PATIENTS WITH METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY. † 843 in PEDIATRIC RESEARCH
  • 1995-05 A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase in NATURE GENETICS
  • 1994-08 Erratum: Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification in NATURE GENETICS
  • 1994-06 Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification in NATURE GENETICS
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