Sophie Visvikis-Siest

Author PubWeight™ 113.69‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 2010 23.08
2 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet 2010 17.89
3 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nat Genet 2009 6.39
4 A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. Nat Genet 2008 5.49
5 Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet 2012 3.21
6 Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature 2011 2.59
7 Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Hum Mol Genet 2012 1.77
8 A genome-wide association search for type 2 diabetes genes in African Americans. PLoS One 2012 1.72
9 Prevalence of loss-of-function FTO mutations in lean and obese individuals. Diabetes 2009 1.54
10 Association of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children. Diabetes 2011 1.31
11 Childhood obesity is associated with shorter leukocyte telomere length. J Clin Endocrinol Metab 2011 1.27
12 Genetic determinants of blood pressure regulation. J Hypertens 2005 1.12
13 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. Clin Chem 2006 1.05
14 Transcription factor and drug-metabolizing enzyme gene expression in lymphocytes from healthy human subjects. Drug Metab Dispos 2007 1.01
15 Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels. Circ Res 2011 0.97
16 Visfatin, low-grade inflammation and body mass index (BMI). Clin Endocrinol (Oxf) 2008 0.90
17 A prospective study on the prevalence of metabolic syndrome among healthy french families: two cardiovascular risk factors (HDL cholesterol and tumor necrosis factor-alpha) are revealed in the offspring of parents with metabolic syndrome. Diabetes Care 2005 0.90
18 Dairy product consumption, calcium intakes, and metabolic syndrome-related factors over 5 years in the STANISLAS study. Nutrition 2012 0.90
19 What is the contribution of two genetic variants regulating VEGF levels to type 2 diabetes risk and to microvascular complications? PLoS One 2013 0.90
20 High prevalence of metabolic syndrome in Iran in comparison with France: what are the components that explain this? Metab Syndr Relat Disord 2012 0.89
21 The lipoprotein lipase serine 447 stop polymorphism is associated with altered serum carotenoid concentrations in the Stanislas Family Study. J Am Coll Nutr 2007 0.89
22 A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels. PLoS One 2012 0.89
23 Expression of inflammatory molecules and associations with BMI in children. Eur J Clin Invest 2010 0.87
24 Capillary isotachophoresis study of lipoprotein network sensitive to apolipoprotein E phenotype. 1. ApoE distribution between lipoproteins. Mol Cell Biochem 2009 0.86
25 Collection and storage of human blood cells for mRNA expression profiling: a 15-month stability study. Clin Chem 2005 0.86
26 Associations of vascular endothelial growth factor (VEGF) with adhesion and inflammation molecules in a healthy population. Cytokine 2012 0.85
27 Determination of ABCB1 polymorphisms and haplotypes frequencies in a French population. Fundam Clin Pharmacol 2007 0.85
28 Polymorphism of the 5-HT2A receptor gene and food intakes in children and adolescents: the Stanislas Family Study. Am J Clin Nutr 2005 0.85
29 Interaction between CYP1A1 T3801C and AHR G1661A polymorphisms according to smoking status on blood pressure in the Stanislas cohort. J Hypertens 2006 0.83
30 Inter-individual variation of inflammatory markers of cardiovascular risks and diseases. Clin Chem Lab Med 2005 0.83
31 Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity. Hum Mol Genet 2012 0.83
32 Association of ABCB1 gene polymorphisms with plasma lipid and apolipoprotein concentrations in the STANISLAS cohort. Clin Chim Acta 2009 0.83
33 Sex-dependent associations of leptin with metabolic syndrome-related variables: the Stanislas study. Obesity (Silver Spring) 2009 0.83
34 Effect of HMGCoA reductase inhibitors on cytochrome P450 expression in endothelial cell line. J Cardiovasc Pharmacol 2007 0.82
35 Heritability for plasma VEGF concentration in the Stanislas family study. Ann Hum Genet 2007 0.81
36 A new single nucleotide polymorphism genotyping method based on gap ligase chain reaction and a microsphere detection assay. Clin Chem Lab Med 2008 0.81
37 Enzymes and pharmacogenetics of cardiovascular drugs. Clin Chim Acta 2007 0.81
38 Analysis of the effect of multiple genetic variants of cardiovascular disease risk on insulin concentration variability in healthy adults of the STANISLAS cohort. The role of FGB-455 G/A polymorphism. Atherosclerosis 2006 0.81
39 Genetic biomarkers of hypertension and future challenges integrating epigenomics. Clin Chim Acta 2012 0.81
40 Association between factor VII polymorphisms and blood pressure: the Stanislas Cohort. Hypertension 2004 0.81
41 Association study of gene polymorphisms involved in vascular alterations in elderly hypertensives with subjective memory complaints. Dement Geriatr Cogn Disord 2010 0.81
42 Personalized therapy and pharmacogenomics: future perspective. Pharmacogenomics 2009 0.80
43 Klotho KL-VS genotype is involved in blood pressure regulation. Clin Chim Acta 2011 0.80
44 Cardiovascular diseases and genome-wide association studies. Clin Chim Acta 2011 0.80
45 Association of classical and related inflammatory markers with high-sensitivity C-reactive protein in healthy individuals: results from the Stanislas cohort. Clin Chem Lab Med 2007 0.80
46 Genetic determinants of leucocyte telomere length in children: a neglected and challenging field. Paediatr Perinat Epidemiol 2015 0.80
47 Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levels. Clin Chim Acta 2010 0.79
48 Natriuretic peptide Val7Met substitution and risk of coronary artery disease in Greek patients with familial hypercholesterolemia. J Clin Lab Anal 2006 0.79
49 Association between EGF and lipid concentrations: a benefit role in the atherosclerotic process? Clin Chim Acta 2009 0.79
50 E-selectin genotypes and risk of type 2 diabetes in women: genetic and environmental contributions to serum soluble E-selectin concentrations. Obes Res 2005 0.78
51 Metabolic syndrome-related composite factors over 5 years in the STANISLAS family study: genetic heritability and common environmental influences. Clin Chim Acta 2010 0.78
52 Alcohol Consumption, Beverage Preference, and Diet in Middle-Aged Men from the STANISLAS Study. J Nutr Metab 2012 0.78
53 Visfatin: the link between inflammation and childhood obesity. Diabetes Care 2009 0.78
54 Relationship between catalase haplotype and arterial aging. Atherosclerosis 2013 0.78
55 Human formyl peptide receptor 1 (FPR1) c.32C>T SNP is associated with decreased soluble E-selectin levels. Pharmacogenomics 2009 0.78
56 Association between TNF and IL-1 bloc polymorphisms and plasma MCP-1 concentration. Atherosclerosis 2006 0.78
57 Association between angiotensin II type 1 receptor gene polymorphism and metabolic syndrome in a young female Iranian population. Arch Med Res 2010 0.77
58 Statins as effectors of key activities involved in apoE-dependent VLDL metabolism: review and hypothesis. Vascul Pharmacol 2007 0.77
59 Different genes and polymorphisms affecting high-density lipoprotein cholesterol levels in Greek familial hypercholesterolemia patients. Genet Test 2006 0.77
60 Leptin expression in Peripheral Blood Mononuclear Cells (PBMCs) is related with blood pressure variability. Clin Chim Acta 2008 0.77
61 Clinical necessity of partitioning of human plasma haptoglobin reference intervals by recently-discovered rs2000999. Clin Chim Acta 2012 0.77
62 Epistatic study reveals two genetic interactions in blood pressure regulation. BMC Med Genet 2013 0.77
63 A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C. J Lipid Res 2012 0.76
64 Pharmacogenomics and cardiovascular drugs: need for integrated biological system with phenotypes and proteomic markers. Eur J Pharmacol 2005 0.76
65 Genetic profiling of human cell lines used as in vitro model to study cardiovascular pathophysiology and pharmacotoxicology. Cell Biol Toxicol 2008 0.76
66 Polymorphisms associated with apolipoprotein B levels in Greek patients with familial hypercholesterolemia. Clin Chem Lab Med 2006 0.76
67 Newly identified synergy between clopidogrel and calcium-channel blockers for blood pressure regulation possibly involves CYP2C19 rs4244285. Int J Cardiol 2013 0.76
68 Clinical interest of point-of-care pharmacogenomic testing: clopidogrel behind warfarin. Pharmacogenomics 2012 0.76
69 Adipokine expression in adipose tissue and in peripheral blood mononuclear cells in children Correlation with BMI and fatty acid content. Clin Chim Acta 2009 0.75
70 Lack of association between EGF 61A>G polymorphism and plasma EGF concentration in the STANISLAS family study. J Invest Dermatol 2006 0.75
71 Influence of genetic variations on levels of inflammatory markers of healthy subjects at baseline and one week after clopidogrel therapy; results of a preliminary study. Int J Mol Sci 2013 0.75
72 Functional epistatic interaction between rs6046G>A in F7 and rs5355C>T in SELE modifies systolic blood pressure levels. PLoS One 2012 0.75
73 Pharmacogenomics: from cell to clinic (Part 1). Pharmacogenomics 2014 0.75
74 Common mutations and polymorphisms predicting adverse cardiovascular events: current view. Pharmacogenomics 2012 0.75
75 Conference Scene: Systems biology and personalized health science and translation. Pharmacogenomics 2013 0.75
76 [Preanalytical variations of proteic biomarkers]. Med Sci (Paris) 2007 0.75
77 Genetic profiling in healthy subjects from the Stanislas cohort based on 24 polymorphisms: effects on biological variables. Clin Chem Lab Med 2008 0.75
78 Genetic and environmental contributions to serum ascorbic acid concentrations: the Stanislas Family Study. Br J Nutr 2006 0.75
79 Genetic determined low response to thienopyridines is associated with higher systemic inflammation in smokers. Pharmacogenomics 2015 0.75
80 Conference scene: pharmacogenomics: from cell to clinic (part 2). Pharmacogenomics 2014 0.75
81 Availability of pharmacogenetic and pharmacogenomic information in anticancer drug monographs in France: personalized cancer therapy. Pharmacogenomics 2011 0.75
82 Capillary isotachophoresis study of lipoprotein network sensitive to apolipoprotein E phenotype. 2. ApoE and apoC-III relations in triglyceride clearance. Mol Cell Biochem 2009 0.75
83 Biological and genetic factors associated with ABCB1 and pregnane-X-receptor expressions in peripheral blood mononuclear cells in the STANISLAS cohort. Drug Metabol Drug Interact 2011 0.75
84 Drug metabolizing enzymes and transporters mRNA in peripheral blood mononuclear cells of healthy subjects: biological variations and importance of pre-analytical steps. Curr Drug Metab 2009 0.75