Ehret, Georg Benedikt

 
Title Year Hits Downloads
Uromodulin and Nephron Mass 2018 29 12
Associations of Urinary Caffeine and Caffeine Metabolites With Arterial Stiffness in a Large Population-Based Study 2018 14 0
Copeptin and insulin resistance: effect modification by age and 11 β-HSD2 activity in a population-based study 2018 28 7
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes 2017 103 1
Urinary cadmium excretion is associated with increased synthesis of cortico- and sex steroids in a population study 2017 162 0
A population-based approach to assess the heritability and distribution of renal handling of electrolytes 2017 174 0
Fibroblast growth factor 23 and markers of mineral metabolism in individuals with preserved renal function 2016 154 67
Associations of Urinary Uromodulin with Clinical Characteristics and Markers of Tubular Function in the General Population 2016 202 67
Relation of 24-hour urinary caffeine and caffeine metabolite excretions with self-reported consumption of coffee and other caffeinated beverages in the general population 2016 310 73
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior 2016 96 0
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function 2016 120 55
CYP17A1 Enzyme Activity Is Linked to Ambulatory Blood Pressure in a Family-Based Population Study 2016 130 1
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes 2016 117 510
Association Analysis of FOXO3 Longevity Variants With Blood Pressure and Essential Hypertension 2016 125 1
Sociodemographic, behavioral and genetic determinants of allostatic load in a Swiss population-based study 2016 270 115
Copeptin is associated with kidney length, renal function, and prevalence of simple cysts in a population-based study 2015 180 73
Mon patient est trop âgé pour une statine : mythes et réalités 2015 123 0
P < 5 × 10(-8) has emerged as a standard of statistical significance for genome-wide association studies 2015 71 0
Heritability of ambulatory and office blood pressure in the Swiss population 2015 165 51
Post-Transcriptional Regulation of Renalase Gene by miR-29 and miR-146 MicroRNAs: Implications for Cardiometabolic Disorders 2015 127 0
Associations of ambulatory blood pressure with urinary caffeine and caffeine metabolite excretions 2015 151 1
Inactive Matrix Gla-Protein Is Associated With Arterial Stiffness in an Adult Population-Based Study 2015 144 0
Dépistage et prise en charge de l’hypertension artérielle chez la personne âgée 2015 119 1
Directional dominance on stature and cognition in diverse human populations 2015 133 77
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study 2015 105 37
Heritability of renal function parameters and electrolyte levels in the swiss population 2015 151 1
Genetic studies of body mass index yield new insights for obesity biology 2015 134 0
Defining the role of common variation in the genomic and biological architecture of adult human height 2014 110 0
Predicting stroke through genetic risk functions: the CHARGE Risk Score Project 2014 263 1
Meeting highlights from the 2013 European Society of Cardiology Heart Failure Association Winter Meeting on Translational Heart Failure Research 2014 187 0
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization 2014 233 1
Epidemiology of masked and white-coat hypertension: the family-based SKIPOGH study 2014 300 91
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia 2014 268 2
Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study 2014 113 25
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations 2014 242 3
Eligibility for renal denervation: experience at 11 European expert centers 2014 259 0
Genetic evidence for a normal-weight "metabolically obese" phenotype linking insulin resistance, hypertension, coronary artery disease and type 2 diabetes 2014 278 0
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index 2014 341 901
Reference values and factors associated with renal resistive index in a family-based population study 2014 485 0
Genetic implication of a novel thiamine transporter in human hypertension 2014 184 1
Discovery and refinement of loci associated with lipid levels 2013 241 0
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study 2013 242 73
La génomique cardiovasculaire: l’exemple de l’hypertension artérielle 2013 281 6
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies 2013 229 0
Influence of CYP2D6 activity on pre-emptive analgesia by the N-methyl-D-aspartate antagonist dextromethorphan in a randomized controlled trial of acute pain 2013 385 421
Fine Mapping and Identification of BMI Loci in African Americans 2013 246 1
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations 2013 270 3
Loci influencing blood pressure identified using a cardiovascular gene-centric array 2013 265 210
The Contribution of the Framingham Heart Study to Gene Identification for Cardiovascular Risk Factors and Coronary Heart Disease 2013 225 0
Heritability, determinants and reference values of renal length: a family-based population study 2013 195 0
Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression 2013 281 1
Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension 2012 296 0
Curing by Burning: What to expect from renal denervation in the treatment of arterial hypertension 2012 270 0
Genome-wide profiling of blood pressure in adults and children 2012 254 228
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron 2012 248 2
Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome 2012 183 224
A multi-SNP locus-association method reveals a substantial fraction of the missing heritability 2012 234 2
Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency 2012 252 81
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk 2011 256 303
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure 2011 183 701
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals 2011 256 295
Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals 2011 295 663
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study 2011 679 681
Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program 2011 242 749
SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension 2011 241 68
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma 2011 256 543
Hypertension arterielle résistante 2010 256 0
Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations 2010 249 0
Common variants at ten loci modulate the QT interval duration in the QTSCD Study 2009 241 1
Genome-wide association study of blood pressure and hypertension 2009 241 1
Multiple loci associated with indices of renal function and chronic kidney disease 2009 569 2
Positional identification of variants of Adamts16 linked to inherited hypertension 2009 249 0
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium 2009 245 1
Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study 2009 169 0
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry 2009 234 1
Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program 2008 220 0
Methadone-associated long QT syndrome: improving pharmacotherapy for dependence on illegal opioids and lessons learned for pharmacology 2007 102 55
Drug-induced long QT syndrome in injection drug users receiving methadone: high frequency in hospitalized patients and risk factors 2006 112 70
Systemic allergic reaction and diffuse bone pain after exposure to a preparation of betamethasone 2005 95 0
QT interval prolongation in patients on methadone with concomitant drugs 2004 105 0
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