David Alexandre Trégouët


Ontology type: schema:Person     


Person Info

NAME

David Alexandre

SURNAME

Trégouët

Publications in SciGraph latest 50 shown

  • 2019-02 A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria in DIABETOLOGIA
  • 2018-12 Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients in NATURE COMMUNICATIONS
  • 2018-12 Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes in CARDIOVASCULAR DIABETOLOGY
  • 2018-12 A systems-approach reveals human nestin is an endothelial-enriched, angiogenesis-independent intermediate filament protein in SCIENTIFIC REPORTS
  • 2018-12 A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients in NATURE COMMUNICATIONS
  • 2018-05 Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study in HUMAN GENETICS
  • 2018-04 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes in NATURE GENETICS
  • 2017-12 Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH in SCIENTIFIC REPORTS
  • 2017-12 Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk in SCIENTIFIC REPORTS
  • 2017-07 Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study in HUMAN GENETICS
  • 2017-02 Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index in MOLECULAR PSYCHIATRY
  • 2017-01-09 Genetic evidence of assortative mating in humans in NATURE HUMAN BEHAVIOUR
  • 2015-12 Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci in NATURE COMMUNICATIONS
  • 2015-03 SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes in DIABETOLOGIA
  • 2015-02 Genetic studies of body mass index yield new insights for obesity biology in NATURE
  • 2014-01 EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension in NATURE GENETICS
  • 2013-12 A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis in BMC MEDICAL GENETICS
  • 2013-05 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture in NATURE GENETICS
  • 2013-05 Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension in NATURE GENETICS
  • 2013-04 Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease in MOLECULAR PSYCHIATRY
  • 2013-01 Large-scale association analysis identifies new risk loci for coronary artery disease in NATURE GENETICS
  • 2012-12 Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: The Athero Gene Study in BMC MEDICAL GENETICS
  • 2011-12 Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels in BMC MEDICAL GENETICS
  • 2011-03 Effect of cytochrome P450 2C19 genotype on voriconazole exposure in cystic fibrosis lung transplant patients in EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY
  • 2010-03 A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians in ENVIRONMENTAL HEALTH AND PREVENTIVE MEDICINE
  • 2010-02 Influence of ghrelin gene polymorphisms on hypertension and atherosclerotic disease in HYPERTENSION RESEARCH
  • 2010-02 Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study in JOURNAL OF MOLECULAR MEDICINE
  • 2009-12 Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM Project in BMC MEDICAL GENETICS
  • 2009-03 Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease in NATURE GENETICS
  • 2009-03 New susceptibility locus for coronary artery disease on chromosome 3q22.3 in NATURE GENETICS
  • 2008-12 Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM Project in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2008-10 Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study in JOURNAL OF MOLECULAR MEDICINE
  • 2007-11 Polymorphisms in 33 inflammatory genes and risk of myocardial infarction—a system genetics approach in JOURNAL OF MOLECULAR MEDICINE
  • 2006-04 Environmental and genetic factors associated with morphine response in the postoperative period in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2004-11 Cox proportional hazards survival regression in haplotype-based association analysis using the Stochastic-EM algorithm in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2004-05 CYP3A5 and MDR1 Genetic Polymorphisms and Cyclosporine Pharmacokinetics After Renal Transplantation in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2004-05 Pharmacogenetics of Acenocoumarol Pharmacodynamics in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2001-10 Serum myeloperoxidase concentration in a healthy population: biological variations, familial resemblance and new genetic polymorphisms in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2001-08 Combined segregation-linkage analysis of plasma thrombin activatable fibrinolysis inhibitor (TAFI) antigen levels with TAFI gene polymorphisms in HUMAN GENETICS
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