| 1 | Associations of VEGF-A-Related Variants with Adolescent Cardiometabolic and Dietary Parameters | 4.7 | 6 | Citations (PDF) |
| 2 | Plasma Amino Acids in NAFLD Patients with Obesity Are Associated with Steatosis and Fibrosis: Results from the MAST4HEALTH Study | 3.5 | 6 | Citations (PDF) |
| 3 | The association of vascular endothelial growth factor related SNPs and circulating iron levels might depend on body mass index | 2.7 | 1 | Citations (PDF) |
| 4 | Association of Dietary Patterns with MRI Markers of Hepatic Inflammation and Fibrosis in the MAST4HEALTH Study | 3.1 | 3 | Citations (PDF) |
| 5 | VEGF-A-related genetic variants protect against Alzheimer’s diseaseAging, 2022, 14, 2524-2536 | 2.5 | 21 | Citations (PDF) |
| 6 | Lipolysis-Stimulated Lipoprotein Receptor Acts as Sensor to Regulate ApoE Release in Astrocytes | 4.5 | 9 | Citations (PDF) |
| 7 | Functional Impairment of Endothelial Colony Forming Cells (ECFC) in Patients with Severe Atherosclerotic Cardiovascular Disease (ASCVD) | 4.5 | 17 | Citations (PDF) |
| 8 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability | 13.9 | 132 | Citations (PDF) |
| 9 | Genome-wide association study of circulating interleukin 6 levels identifies novel loci | 3.0 | 52 | Citations (PDF) |
| 10 | Effect of Mastiha supplementation on NAFLD: The MAST4HEALTH Randomised, Controlled Trial | 4.1 | 31 | Citations (PDF) |
| 11 | Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD | 5.1 | 23 | Citations (PDF) |
| 12 | Epigenome-wide association study detects a novel loci associated with central obesity in healthy subjects | 1.8 | 6 | Citations (PDF) |
| 13 | Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants | 52.8 | 2,827 | Citations (PDF) |
| 14 | Dietary Patterns, Blood Pressure and the Glycemic and Lipidemic Profile of Two Teenage, European Populations | 4.7 | 10 | Citations (PDF) |
| 15 | A genetic determinant of VEGF-A levels is associated with telomere attritionAging, 2021, 13, 23517-23526 | 2.5 | 2 | Citations (PDF) |
| 16 | National trends in total cholesterol obscure heterogeneous changes in HDL and non-HDL cholesterol and total-to-HDL cholesterol ratio: a pooled analysis of 458 population-based studies in Asian and Western countries | 5.1 | 53 | Citations (PDF) |
| 17 | Telomere length determinants in childhood | 2.4 | 56 | Citations (PDF) |
| 18 | Milestones in Personalized Medicine: From the Ancient Time to Nowadays—the Provocation of COVID-19 | 2.4 | 42 | Citations (PDF) |
| 19 | Height and body-mass index trajectories of school-aged children and adolescents from 1985 to 2019 in 200 countries and territories: a pooled analysis of 2181 population-based studies with 65 million participants | 52.8 | 343 | Citations (PDF) |
| 20 | Repositioning of the global epicentre of non-optimal cholesterol | 38.7 | 237 | Citations (PDF) |
| 21 | Epigenome-wide association study in healthy individuals identifies significant associations with DNA methylation and PBMC extract VEGF-A concentration | 4.0 | 9 | Citations (PDF) |
| 22 | Increased risk of hypercholesterolemia in a French and Lebanese population due to an interaction between rs2569190 in CD14 and gender | 1.6 | 1 | Citations (PDF) |
| 23 | TERC Variants Associated with Short Leukocyte Telomeres: Implication of Higher Early Life Leukocyte Telomere Attrition as Assessed by the Blood-and-Muscle Model | 4.8 | 4 | Citations (PDF) |
| 24 | Obesity status modifies the association between rs7556897T>C in the intergenic region <i>SLC19A3</i>-<i>CCL20</i> and blood pressure in French children | 2.4 | 3 | Citations (PDF) |
| 25 | Peripheral blood mononuclear cells extracts VEGF protein levels and VEGF mRNA: Associations with inflammatory molecules in a healthy population | 2.4 | 11 | Citations (PDF) |
| 26 | 4th ESPT Summer School: Precision Medicine and Personalised Health | 1.6 | 0 | Citations (PDF) |
| 27 | Genetic determinants of circulating haptoglobin concentration | 1.6 | 17 | Citations (PDF) |
| 28 | Epigenome-Wide Association Study (EWAS) of Blood Lipids in Healthy Population from STANISLAS Family Study (SFS) | 4.5 | 17 | Citations (PDF) |
| 29 | Pleiotropy of ABO gene: correlation of rs644234 with E-selectin and lipid levels | 2.4 | 10 | Citations (PDF) |
| 30 | Contributions of mean and shape of blood pressure distribution to worldwide trends and variations in raised blood pressure: a pooled analysis of 1018 population-based measurement studies with 88.6 million participants | 5.1 | 76 | Citations (PDF) |
| 31 | The Relationship Between Vascular Endothelial Growth Factor Cis- and Trans-Acting Genetic Variants and Metabolic Syndrome | 0.8 | 8 | Citations (PDF) |
| 32 | Effect of <i>LSR</i> polymorphism on blood lipid levels and age‐specific epistatic interaction with the <i>APOE</i> common polymorphism | 2.1 | 5 | Citations (PDF) |
| 33 | A transnational collaborative network dedicated to the study and applications of the vascular endothelial growth factor-A in medical practice: the VEGF Consortium | 2.4 | 1 | Citations (PDF) |
| 34 | VEGF-A is associated with early degenerative changes in cartilage and subchondral bone | 1.8 | 18 | Citations (PDF) |
| 35 | Personalised Medicine: The Odyssey from Hope to Practice | 2.6 | 10 | Citations (PDF) |
| 36 | Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders | 6.5 | 416 | Citations (PDF) |
| 37 | The future of telomere length in personalized medicine | 6.0 | 35 | Citations (PDF) |
| 38 | The polymorphism rs6918289 located in the downstream region of the TREM2 gene is associated with TNF-α levels and IMT-F | 3.5 | 3 | Citations (PDF) |
| 39 | Epistatic interaction of apolipoprotein E and lipolysis-stimulated lipoprotein receptor genetic variants is associated with Alzheimer's disease | 3.4 | 4 | Citations (PDF) |
| 40 | VEGF-related polymorphisms identified by GWAS and risk for major depression | 5.5 | 46 | Citations (PDF) |
| 41 | 8th Santorini Conference: Systems medicine and personalized health and therapy, Santorini, Greece, 3–5 October 2016 | 1.0 | 5 | Citations (PDF) |
| 42 | Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults | 52.8 | 6,316 | Citations (PDF) |
| 43 | Next generation sequencing and immuno-histochemistry profiling identify numerous biomarkers for personalized therapy of endometrioid endometrial carcinoma | 2.4 | 1 | Citations (PDF) |
| 44 | IL6R haplotype rs4845625*T/rs4537545*C is a risk factor for simultaneously high CRP, LDL and ApoB levels | 3.8 | 7 | Citations (PDF) |
| 45 | Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19·1 million participants | 52.8 | 2,027 | Citations (PDF) |
| 46 | Pharmacogenomic Challenges in Cardiovascular Diseases: Examples of Drugs and Considerations for Future Integration in Clinical Practice | 2.3 | 9 | Citations (PDF) |
| 47 | TREM-1 SNP rs2234246 regulates TREM-1 protein and mRNA levels and is associated with plasma levels of L-selectin | 2.4 | 34 | Citations (PDF) |
| 48 | La Pharmacogénomique, meilleur exemple de médecine personnalisée | 0.1 | 0 | Citations (PDF) |
| 49 | Cardiovascular diseases-related GNB3 C825T polymorphism has a significant sex-specific effect on serum soluble E-selectin levels | 4.1 | 6 | Citations (PDF) |
| 50 | Pro- and anti-angiogenic VEGF mRNAs in autoimmune thyroid diseases | 3.2 | 7 | Citations (PDF) |
| 51 | Plasma VEGF-related polymorphisms are implied in autoimmune thyroid diseases | 3.2 | 8 | Citations (PDF) |
| 52 | Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies | 3.3 | 62 | Citations (PDF) |
| 53 | De l’écogénétique à la pharmacogénomique par le stress oxydant | 0.1 | 0 | Citations (PDF) |
| 54 | Le Professeur Gérard Siest nous a quittés (1936-2016) | 0.1 | 0 | Citations (PDF) |
| 55 | Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults | 2.0 | 32 | Citations (PDF) |
| 56 | Genetic Determined Low Response to Thienopyridines is Associated with Higher Systemic Inflammation in Smokers | 1.6 | 0 | Citations (PDF) |
| 57 | Influence of inflammation on cardiovascular protective effects of cytochrome P450 epoxygenase-derived epoxyeicosatrienoic acids | 3.9 | 32 | Citations (PDF) |
| 58 | Human cytochrome P450 epoxygenases: Variability in expression and role in inflammation-related disorders 2014, 144, 134-161 | | 90 | Citations (PDF) |
| 59 | Epistatic study reveals two genetic interactions in blood pressure regulation | 2.0 | 13 | Citations (PDF) |
| 60 | Associations of vascular endothelial growth factor (VEGF) with adhesion and inflammation molecules in a healthy population | 3.7 | 33 | Citations (PDF) |
| 61 | Dairy product consumption, calcium intakes, and metabolic syndrome–related factors over 5 years in the STANISLAS study | 2.9 | 64 | Citations (PDF) |
| 62 | Relationship between catalase haplotype and arterial aging | 1.6 | 14 | Citations (PDF) |
| 63 | Newly identified synergy between clopidogrel and calcium-channel blockers for blood pressure regulation possibly involves CYP2C19 rs4244285 | 2.3 | 4 | Citations (PDF) |
| 64 | A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C | 3.7 | 30 | Citations (PDF) |
| 65 | What Is the Contribution of Two Genetic Variants Regulating VEGF Levels to Type 2 Diabetes Risk and to Microvascular Complications? | 2.4 | 39 | Citations (PDF) |
| 66 | Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals | 3.3 | 453 | Citations (PDF) |
| 67 | Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity | 3.0 | 40 | Citations (PDF) |
| 68 | Alcohol Consumption, Beverage Preference, and Diet in Middle-Aged Men from the STANISLAS Study | 2.1 | 21 | Citations (PDF) |
| 69 | Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans | 3.0 | 235 | Citations (PDF) |
| 70 | Genetic biomarkers of hypertension and future challenges integrating epigenomics | 1.6 | 32 | Citations (PDF) |
| 71 | Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels | 1.6 | 15 | Citations (PDF) |
| 72 | Clinical necessity of partitioning of human plasma haptoglobin reference intervals by recently-discovered rs2000999 | 1.6 | 16 | Citations (PDF) |
| 73 | High Prevalence of Metabolic Syndrome in Iran in Comparison with France: What Are the Components That Explain This? | 2.1 | 51 | Citations (PDF) |
| 74 | A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans | 2.4 | 204 | Citations (PDF) |
| 75 | A Genome-Wide Association Study Identifies rs2000999 as a Strong Genetic Determinant of Circulating Haptoglobin Levels | 2.4 | 38 | Citations (PDF) |
| 76 | Functional Epistatic Interaction between rs6046G>A in F7 and rs5355C>T in SELE Modifies Systolic Blood Pressure Levels | 2.4 | 8 | Citations (PDF) |
| 77 | Childhood Obesity Is Associated with Shorter Leukocyte Telomere Length | 4.2 | 139 | Citations (PDF) |
| 78 | Klotho KL-VS genotype is involved in blood pressure regulation | 1.6 | 20 | Citations (PDF) |
| 79 | Cardiovascular diseases and genome-wide association studies | 1.6 | 22 | Citations (PDF) |
| 80 | Availability of Pharmacogenetic and Pharmacogenomic Information in Anticancer Drug Monographs in France: Personalized Cancer Therapy | 1.6 | 4 | Citations (PDF) |
| 81 | Identification of
<i>cis</i>
- and
<i>trans</i>
-Acting Genetic Variants Explaining Up to Half the Variation in Circulating Vascular Endothelial Growth Factor Levels | 12.5 | 81 | Citations (PDF) |
| 82 | Association of Genetic Loci With Glucose Levels in Childhood and Adolescence | 4.4 | 111 | Citations (PDF) |
| 83 | Biological and genetic factors associated with ABCB1 and pregnane-X-receptor expressions in peripheral blood mononuclear cells in the STANISLAS cohort | 0.3 | 3 | Citations (PDF) |
| 84 | Association Between Angiotensin II Type 1 Receptor Gene Polymorphism and Metabolic Syndrome in a Young Female Iranian Population | 2.7 | 17 | Citations (PDF) |
| 85 | Expression of inflammatory molecules and associations with BMI in children | 3.3 | 24 | Citations (PDF) |
| 86 | Sex‐dependent Associations of Leptin With Metabolic Syndrome–related Variables: The Stanislas Study | 4.2 | 27 | Citations (PDF) |
| 87 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | 26.1 | 2,774 | Citations (PDF) |
| 88 | Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals | 4.4 | 98 | Citations (PDF) |
| 89 | Metabolic syndrome-related composite factors over 5years in the STANISLAS Family Study: Genetic heritability and common environmental influences | 1.6 | 15 | Citations (PDF) |
| 90 | New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk | 26.1 | 2,098 | Citations (PDF) |
| 91 | Personalized Therapy and Pharmacogenomics: Future Perspective | 1.6 | 9 | Citations (PDF) |
| 92 | Capillary isotachophoresis study of lipoprotein network sensitive to apolipoprotein E phenotype. 2. ApoE and apoC-III relations in triglyceride clearance | 3.3 | 3 | Citations (PDF) |
| 93 | Capillary isotachophoresis study of lipoprotein network sensitive to apolipoprotein E phenotype. 1. ApoE distribution between lipoproteins | 3.3 | 3 | Citations (PDF) |
| 94 | Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations | 26.1 | 609 | Citations (PDF) |
| 95 | Association between EGF and lipid concentrations: A benefit role in the atherosclerotic process? | 1.6 | 11 | Citations (PDF) |
| 96 | Association of ABCB1 gene polymorphisms with plasma lipid and apolipoprotein concentrations in the STANISLAS cohort | 1.6 | 23 | Citations (PDF) |
| 97 | Adipokine expression in adipose tissue and in peripheral blood mononuclear cells in children | 1.6 | 7 | Citations (PDF) |
| 98 | Association of human cathelicidin (hCAP-18/LL-37) gene expression with cardiovascular disease risk factors | 3.4 | 32 | Citations (PDF) |
| 99 | Human Formyl Peptide Receptor 1 (
<i>FPR1</i>
) c.32C>T SNP is Associated with Decreased Soluble E-selectin Levels | 1.6 | 8 | Citations (PDF) |
| 100 | Parental Precocious Influences on Offspring Cardiovascular Risk Markers: An Exploratory Study in the Stanislas Cohort | 1.4 | 0 | Citations (PDF) |
| 101 | Candidate Gene Microarray Analysis in Peripheral Blood Cells for Studying Hypertension/Obesity | 1.4 | 6 | Citations (PDF) |
| 102 | Drug Metabolizing Enzymes and Transporters mRNA in Peripheral Blood Mononuclear Cells of Healthy Subjects: Biological Variations and Importance of Preanalytical Steps | 1.2 | 5 | Citations (PDF) |
| 103 | Genomics and the Prospects of Existing and Emerging Therapeutics for Cardiovascular Diseases | 2.4 | 12 | Citations (PDF) |
| 104 | Five-year alterations in BMI are associated with clustering of changes in cardiovascular risk factors in a gender-dependant way: the Stanislas study | 3.2 | 27 | Citations (PDF) |
| 105 | Visfatin, low‐grade inflammation and body mass index (BMI) | 2.5 | 40 | Citations (PDF) |
| 106 | Statins as effectors of key activities involved in apoE-dependent VLDL metabolism: Review and hypothesis | 2.5 | 10 | Citations (PDF) |
| 107 | Leptin expression in Peripheral Blood Mononuclear Cells (PBMCs) is related with blood pressure variability | 1.6 | 16 | Citations (PDF) |
| 108 | Transcription Factor and Drug-Metabolizing Enzyme Gene Expression in Lymphocytes from Healthy Human Subjects | 3.6 | 81 | Citations (PDF) |
| 109 | A new single nucleotide polymorphism genotyping method based on gap ligase chain reaction and a microsphere detection assay | 2.4 | 4 | Citations (PDF) |
| 110 | The STANISLAS Cohort: a 10-year follow-up of supposed healthy families. Gene-environment interactions, reference values and evaluation of biomarkers in prevention of cardiovascular diseases | 2.4 | 51 | Citations (PDF) |
| 111 | Genetic profiling in healthy subjects from the Stanislas cohort based on 24 polymorphisms: effects on biological variables | 2.4 | 1 | Citations (PDF) |
| 112 | Genetic profiling of human cell lines used as in vitro model to study cardiovascular pathophysiology and pharmacotoxicology | 5.0 | 8 | Citations (PDF) |
| 113 | Association of classical and related inflammatory markers with high-sensitivity C-reactive protein in healthy individuals: results from the Stanislas cohort | 2.4 | 11 | Citations (PDF) |
| 114 | Effect of HMGCoA Reductase Inhibitors on Cytochrome P450 Expression in Endothelial Cell Line | 2.1 | 23 | Citations (PDF) |
| 115 | Enzymes and pharmacogenetics of cardiovascular drugs | 1.6 | 40 | Citations (PDF) |
| 116 | Analysis of the effect of multiple genetic variants of cardiovascular disease risk on insulin concentration variability in healthy adults of the STANISLAS cohort | 1.6 | 15 | Citations (PDF) |
| 117 | Association between TNF and IL-1 bloc polymorphisms and plasma MCP-1 concentration | 1.6 | 12 | Citations (PDF) |
| 118 | Pharmacogenomics and antihypertensive drugs: a path toward personalized medicine | 1.4 | 4 | Citations (PDF) |
| 119 | Une étude prospective de la prévalence du syndrome métabolique dans des familles françaises supposées saines | 1.1 | 1 | Citations (PDF) |
| 120 | Pharmacogénomique et pharmacoprotéomique | 1.1 | 7 | Citations (PDF) |
| 121 | Peripheral blood mononuclear cells (PBMCs): a possible model for studying cardiovascular biology systems | 2.4 | 58 | Citations (PDF) |
| 122 | Variations pré-analytiques des biomarqueursprotéiques | 0.2 | 2 | Citations (PDF) |
| 123 | Heritability of serum hs-CRP concentration and 5-year changes in the Stanislas family study: association with apolipoprotein E alleles | 3.8 | 12 | Citations (PDF) |
| 124 | Lack of Association between EGF 61A>G Polymorphism and Plasma EGF Concentration in the STANISLAS Family Study | 2.3 | 3 | Citations (PDF) |
| 125 | Heritability for Plasma VEGF Concentration in the Stanislas Family Study | 1.2 | 34 | Citations (PDF) |
| 126 | Determination of ABCB1 polymorphisms and haplotypes frequencies in a French population | 2.5 | 42 | Citations (PDF) |
| 127 | Genetic and environmental contributions to serum ascorbic acid concentrations: the Stanislas Family Study | 2.5 | 2 | Citations (PDF) |
| 128 | Interaction between CYP1A1 T3801C and AHR G1661A polymorphisms according to smoking status on blood pressure in the Stanislas cohort | 2.3 | 21 | Citations (PDF) |
| 129 | Genetic variants predisposing to cardiovascular disease | 4.1 | 48 | Citations (PDF) |
| 130 | Natriuretic peptide Val7Met substitution and risk of coronary artery disease in Greek patients with familial hypercholesterolemia | 2.8 | 12 | Citations (PDF) |
| 131 | Biological Determinants of and Reference Values for Plasma Interleukin-8, Monocyte Chemoattractant Protein-1, Epidermal Growth Factor, and Vascular Endothelial Growth Factor: Results from the STANISLAS Cohort | 1.1 | 55 | Citations (PDF) |
| 132 | Polymorphisms associated with apolipoprotein B levels in Greek patients with familial hypercholesterolemia | 2.4 | 3 | Citations (PDF) |
| 133 | Different Genes and Polymorphisms Affecting High-Density Lipoprotein Cholesterol Levels in Greek Familial Hypercholesterolemia Patients | 0.0 | 10 | Citations (PDF) |
| 134 | E‐Selectin Genotypes and Risk of Type 2 Diabetes in Women: Genetic and Environmental Contributions to Serum Soluble E‐Selectin Concentrations | 4.2 | 5 | Citations (PDF) |
| 135 | Association of CYP2A6*1B genetic variant with the amount of smoking in French adults from the Stanislas cohort | 2.8 | 36 | Citations (PDF) |
| 136 | Pharmacogenomics and cardiovascular drugs: Need for integrated biological system with phenotypes and proteomic markers | 4.4 | 33 | Citations (PDF) |
| 137 | Apolipoprotein E polymorphism is not associated with lipid levels and coronary artery disease in Greek patients with familial hypercholesterolaemia | 3.0 | 20 | Citations (PDF) |
| 138 | Polymorphism of the 5-HT2A receptor gene and food intakes in children and adolescents: the Stanislas Family Study | 4.9 | 32 | Citations (PDF) |
| 139 | Collection and Storage of Human Blood Cells for mRNA Expression Profiling: A 15-Month Stability Study | 1.1 | 37 | Citations (PDF) |
| 140 | Inter-individual variation of inflammatory markers of cardiovascular risks and diseases | 2.4 | 18 | Citations (PDF) |
| 141 | Down-regulation of astroglial CYP2C, glucocorticoid receptor and constitutive androstane receptor genes in response to cocaine in human U373 MG astrocytoma cells | 0.6 | 25 | Citations (PDF) |
| 142 | Association Between Factor VII Polymorphisms and Blood Pressure | 6.9 | 8 | Citations (PDF) |
| 143 | Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight | 1.6 | 64 | Citations (PDF) |
