Circulating biomarkers search for vasospasm occurrence in subarachnoid hemorrhage patients. |
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Development of gene-prioritising methods using statistical genetics and clinical annotation for rare genetic disorders |
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Développement de méthodes de priorisation de gènes pour les maladies génétiques rares grâce à un test paramétrique de statistique génétique et à l'annotation clinique. |
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Épidémiologie épi-génétique de biomarqueurs du risque cardiovasculaire : intérêt de l'étude de la méthylation de l'ADN à partir d'échantillons sanguins |
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Epigenetics of Cardiometabolic Biomarkers Through the Study of DNA Methylation Patterns from Blood Samples. |
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Les équations d'estimation : principes et applications à l'étude de la composante familiale et génétique des maladies multifactorielles |
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Etude de l'importance génétique, moléculaire et physiologique du gène PHACTR1, récemment identifié comme central dans les pathologies vasculaires |
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Etude des facteurs génétiques de variabilité phénotypique dans les formes syndromiques d'anévrismes de l'aorte thoracique |
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Étude des interactions entre la fonction rénale, la thrombose artérielle et la thrombose veineuse par une approche génétique |
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Exposition aux endotoxines : influence de l'alimentation et rôle dans le vieillissement cognitif |
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Genetic and environmental factors study of type 2 diabetes complications. |
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Genetic and plasmatic variations of microRNAs : impact on haemostatic traits. |
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Genetic factors reponsible of clinical variability in familial forms of thoracic aortic aneurysm. |
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A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis |
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GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm |
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Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM Project |
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Homocysteine concentration in coronary artery disease: Influence of three common single nucleotide polymorphisms. |
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Identification de variants génétiques associés à la thrombose veineuse |
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Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome |
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Identification of novel actors implicated in HDL metabolism : impact on cardiovascular diseases. |
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Identification of venous thromboembolism risk factors. |
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Influence of coronary artery disease-associated genetic variants on risk of venous thromboembolism. |
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Influence of ghrelin gene polymorphisms on hypertension and atherosclerotic disease. |
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KNG1 Ile581Thr and susceptibility to venous thrombosis |
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Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM Project |
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Large-scale association analysis identifies new risk loci for coronary artery disease |
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Link between heritability and prediction of complex phenotypes in human genomics : approaching the problem using ridge regression on population data. |
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Macrothrombocytopenia and dense granule deficiency associated with FLI1 variants: ultrastructural and pathogenic features. |
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Merkel cell polyomavirus infection occurs during early childhood and is transmitted between siblings |
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Metabolic determinants are much more important than genetic polymorphisms in determining the PAI-1 activity and antigen plasma concentrations: a family study with part of the Stanislas Cohort. |
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Méthodes statistiques pour la prise en compte de différentes sources de biais dans les études d'association à grande échelle. |
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Méthodologie statistique pour l'analyse de polymorphismes génétiques dans une étude de type cas-cohorte : application au projet MORGAME |
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MFGE8 does not influence chorio-retinal homeostasis or choroidal neovascularization in vivo. |
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Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation |
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miR-322 regulates insulin signaling pathway and protects against metabolic syndrome-induced cardiac dysfunction in mice |
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miR-421 and miR-30c inhibit SERPINE 1 gene expression in human endothelial cells |
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Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control |
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Multilocus genetic risk scores for venous thromboembolism risk assessment |
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A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm. |
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A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies. |
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New susceptibility loci associated with kidney disease in type 1 diabetes |
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No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects |
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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 |
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PARVG Gene Polymorphism and Operational Renal Allograft Tolerance |
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PDGFB, a new candidate plasma biomarker for venous thromboembolism: results from the VEREMA affinity proteomics study. |
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Pharmacogenetic assessment of toxicity and outcome in patients with metastatic colorectal cancer treated with LV5FU2, FOLFOX, and FOLFIRI: FFCD 2000-05. |
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Pharmacogenetics of acenocoumarol pharmacodynamics. |
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Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach. |
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Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study |
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Precision Medicine and Prediction in Pharmacology : Pharmacodynamics and Pharmacogenetics approaches to the evaluation of cardiovascular drugs. |
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Prediction of Causal Candidate Genes in Coronary Artery Disease LociSignificance |
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Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans |
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Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk. |
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Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes |
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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. |
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Quantification of thrombin activatable fibrinolysis inhibitor (TAFI) gene polymorphism effects on plasma levels of TAFI measured with assays insensitive to isoform-dependent artefact |
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Recherche de biomarqueurs circulants de la survenue du vasospasme chez des patients souffrant d'hémorragie sous-arachnoïdienne |
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Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data |
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Robust validation of methylation levels association at CPT1A locus with lipid plasma levels |
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The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis |
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Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages |
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Serum myeloperoxidase concentration in a healthy population: biological variations, familial resemblance and new genetic polymorphisms |
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Sex-specific effect of CPB2 Ala147Thr but not Thr325Ile variants on the risk of venous thrombosis: A comprehensive meta-analysis |
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Shared genetic regulatory networks for cardiovascular disease and type 2 diabetes in multiple populations of diverse ethnicities in the United States |
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Single nucleotide polymorphisms in an intergenic chromosome 2q region associated with tissue factor pathway inhibitor plasma levels and venous thromboembolism. |
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Single nucleotide polymorphisms in MMP1 and MMP3 gene promoters as risk factor in head and neck squamous cell carcinoma |
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Small platelet microparticle levels are increased in pulmonary arterial hypertension. |
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SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes |
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Sources and consequences of regulatory variants in humans. |
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Specific haplotypes of the P-selectin gene are associated with myocardial infarction. |
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Statistical methodologies for the analysis of genetic determinants of venous thromboembolic disease and its complications. |
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Statistical methods to account for different sources of bias in Genome-Wide association studies |
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Stratégies de recherches de phénomènes d'interactions dans les maladies multifactorielles |
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Study of interactions between renal function, arterial thrombosis and venous thrombosis using a genetic approach. |
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Thrombin Generation Potential and Whole-Blood DNA methylation |
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Transcriptome-Wide Analysis Identifies Novel Associations With Blood Pressure |
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Transcriptomic characterization of endothelial cells from HHT and PAH patients carrying ALK1 mutations to propose new therapeutic approaches for these two vascular diseases. |
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Variation génétique et plasmatique des microARNs : impact sur les paramètres biologiques de l'hémostase |
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Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II. |
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What is currently known about the genetics of venous thromboembolism at the dawn of next generation sequencing technologies |
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