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Biomarker and cognitive decline in atrial fibrillation : a prospective cohort studyScientific reports
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2025 34 17
Innovation pour les patients avec hypertension artérielleRevue médicale suisse
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2024 1 0
Dysfonction érectile chez le patient hypertenduRevue médicale suisse
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2024 1 0
Heart rate variability and stroke or systemic embolism in patients with atrial fibrillationHeart rhythm
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2024 51 58
Host-symbiont interactions in Angomonas deanei include the evolution of a host-derived dynamin ring around the endosymbiont division siteCurrent biology
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2023 86 54
Mesure automatique et non observée de la pression artérielle : un outil précieux pour le clinicienRevue médicale suisse
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2023 4 1
Sex differences of vascular brain lesions in patients with atrial fibrillationOpen heart
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2022 212 67
Long-term risk of adverse outcomes according to atrial fibrillation typeScientific reports
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2022 218 92
Uncovering a Genetic Polymorphism Located in Huntingtin Associated Protein 1 in Modulation of Central Pain Sensitization Signaling PathwaysFrontiers in neuroscience
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2022 416 95
Silent brain infarcts impact on cognitive function in atrial fibrillationEuropean heart journal
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2022 249 128
Dernières recommandations européennes sur les dyslipidémiesRevue médicale suisse
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2022 375 563
Increased glucocorticoid metabolism in diabetic kidney diseasePloS one
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2022 101 103
The international database of central arterial properties for risk stratification : research objectives and baseline characteristics of participantsAmerican journal of hypertension
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2022 165 84
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individualsCommunications biology
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2022 173 35
Reduced adrenal stress response in patients on PCSK9 inhibitor therapyAtherosclerosis
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2021 235 0
Gene regulation contributes to explain the impact of early life socioeconomic disadvantage on adult inflammatory levels in two cohort studiesScientific reports
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2021 250 196
Heritability and association with distinct genetic loci of erythropoietin levels in the general populationHaematologica
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2021 278 70
Une baisse du cholestérol LDL de longue durée : enfin le silenceRevue médicale suisse
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2021 290 0
Assessment of a strategy combining ambulatory blood pressure, adherence monitoring and a standardised triple therapy in resistant hypertensionBlood pressure
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2021 240 157
Lipoprotein(a) levels are not independently associated with endogenous steroid hormone levels, in contrast to other non-genetic and genetic factors: the population-based SKIPOGH studyEuropean heart journal
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2021 234 0
Hypertension and heart failure with preserved ejection fraction: position paper by the European Society of HypertensionJournal of hypertension
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2021 169 0
Insulin-like growth factor-binding protein 7 and risk of congestive heart failure hospitalization in patients with atrial fibrillationHeart Rhythm
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2021 394 0
Changes of lipoprotein(a) levels with endogenous steroid hormonesEuropean journal of clinical investigation
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2021 303 307
Sex- and age-specific reference intervals for diagnostic ratios reflecting relative activity of steroidogenic enzymes and pathways in adultsPloS one
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2021 277 158
Ambulatory Blood Pressure in Relation to Plasma and Urinary ManganeseHypertension
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2020 303 119
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conductionNature communications
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2020 199 51
Blood Pressure and Brain Lesions in Patients With Atrial FibrillationHypertension
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2020 620 295
Analysis of putative cis-regulatory elements regulating blood pressure variationHuman molecular genetics
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2020 190 106
Feasibility and safety of high-intensity interval training for the rehabilitation of geriatric inpatients (HIITERGY) a pilot randomized studyBMC Geriatrics
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2020 284 186
Measured and Genotyped Differences in Blood Pressure and the Usefulness of Precise Extreme Phenotypes Based on Cardiovascular Magnetic ResonanceHypertension
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2019 264 1
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaNature Communications
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2019 386 222
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levelsNature Genetics
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2019 327 132
A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressureHuman Molecular Genetics
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2019 462 1
Reference intervals for the urinary steroid metabolome: The impact of sex, age, day and night time on human adult steroidogenesisPLOS ONE
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2019 300 192
Relationships of overt and silent brain lesions with cognitive function in patients with atrial fibrillationJournal of the American College of Cardiology
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2019 446 0
Renal resistive index is associated with inactive Matrix Gla (γ-carboxyglutamate) protein in an adult population-based studyJournal of the American Heart Association
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2019 367 131
Parathyroid hormone and plasma phosphate are predictors of soluble α-klotho levels in adults of European descentJournal of Clinical Endocrinology and Metabolism
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2019 383 140
Urinary sex steroid and glucocorticoid hormones are associated with muscle mass and strength in healthy adultsJournal of Clinical Endocrinology and Metabolism
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2019 323 0
A catalog of genetic loci associated with kidney function from analyses of a million individualsNature Genetics
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2019 355 236
Association of FMO3 variants with blood pressure in the atherosclerosis risk in communities studyInternational journal of hypertension
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2019 330 153
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in AfricaCell
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2019 383 1
Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31European Journal of Human Genetics
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2019 241 117
In the Age of Genomics, Is it Still Worth it to Investigate Individual Loci?Hypertension
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2019 305 2
Complex cardiovascular diseases: the genetics of arterial hypertensionThe ESC Textbook of Cardiovascular Medicine
2019 323 0
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activityNature Communications
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2018 319 231
Trans-ethnic analysis of metabochip data identifies two new loci associated with BMIInternational Journal of Obesity
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2018 423 0
Genes for Preeclampsia: An Opportunity for Blood Pressure GenomicsHypertension
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2018 293 156
Uromodulin and Nephron MassClinical Journal of the American Society of Nephrology
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2018 460 319
Associations of Urinary Caffeine and Caffeine Metabolites With Arterial Stiffness in a Large Population-Based StudyMayo Clinic Proceedings
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2018 476 1
Genetics of HypertensionHypertension : A Compandion To Braunwald's Heart Diease
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2018 310 91
Epidemiological and histological findings implicate matrix Gla protein in diastolic left ventricular dysfunctionPLOS ONE
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2018 487 185
Association of 24-Hour Blood Pressure With Urinary Sodium Excretion in Healthy AdultsAmerican Journal of Hypertension
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2018 426 1
Copeptin and insulin resistance: effect modification by age and 11 β-HSD2 activity in a population-based studyJournal of Endocrinological Investigation
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2018 518 480
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traitsNature Genetics
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2018 361 0
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood PressureAmerican Journal of Human Genetics
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2018 409 290
A comprehensive evaluation of the genetic architecture of sudden cardiac arrestEuropean Heart Journal
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2018 289 0
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestriesPLOS ONE
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2018 306 253
Molecular pathways associated with blood pressure and hexadecanedioate levelsPLOS ONE
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2017 326 146
Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestryJournal of Hypertension
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2017 310 0
Design of the Swiss Atrial Fibrillation Cohort Study (Swiss-AF): structural brain damage and cognitive decline among patients with atrial fibrillationSwiss Medical Weekly
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2017 338 256
Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering allelesEuropean Journal of Preventive Cardiology
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2017 339 116
Genetic loci associated with heart rate variability and their effects on cardiac disease riskNature Communications
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2017 294 193
Urinary cadmium excretion is associated with increased synthesis of cortico- and sex steroids in a population studyJournal of Clinical Endocrinology and Metabolism
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2017 625 0
Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populationsInternational Journal of Obesity
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2017 333 0
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the KidneyHypertension
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2017 334 0
A population-based approach to assess the heritability and distribution of renal handling of electrolytesKidney International
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2017 625 0
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variationNature Genetics
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2017 290 0
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic PhenotypesJournal of the American Society of Nephrology
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2017 527 1
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 IndividualsCirculation: Cardiovascular Genetics
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2017 289 0
Next Steps for Gene Identification in Primary Hypertension GenomicsHypertension
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2017 289 127
Association Analysis of FOXO3 Longevity Variants With Blood Pressure and Essential HypertensionAmerican journal of hypertension
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2016 472 1
Relation of 24-hour urinary caffeine and caffeine metabolite excretions with self-reported consumption of coffee and other caffeinated beverages in the general populationNutrition & Metabolism
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2016 1,144 66
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart diseaseScience Translational Medicine
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2016 298 0
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behaviorHuman Molecular Genetics
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2016 598 0
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney functionNature communications
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2016 514 443
Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African AmericansPLOS ONE
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2016 309 186
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individualsNature Genetics
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2016 348 0
Sociodemographic, behavioral and genetic determinants of allostatic load in a Swiss population-based studyPsychoneuroendocrinology
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2016 1,136 454
The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractilityScientific Reports
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2016 295 157
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in DiabetesDiabetes
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2016 543 142
CYP17A1 Enzyme Activity Is Linked to Ambulatory Blood Pressure in a Family-Based Population StudyAmerican journal of hypertension
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2016 545 1
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait lociNature Genetics
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2016 328 0
Associations of Urinary Uromodulin with Clinical Characteristics and Markers of Tubular Function in the General PopulationClinical journal of the American Society of Nephrology
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2016 666 384
Fibroblast growth factor 23 and markers of mineral metabolism in individuals with preserved renal functionKidney international
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2016 607 332
Protocol of the Swiss Longitudinal Cohort Study (SWICOS) in rural SwitzerlandBMJ Open
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2016 334 116
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary DiseaseNew England Journal of Medicine
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2016 366 122
Heritability of renal function parameters and electrolyte levels in the swiss populationJournal of hypertension
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2015 499 1
Copeptin is associated with kidney length, renal function, and prevalence of simple cysts in a population-based studyJournal of the American Society of Nephrology
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2015 585 96
Dépistage et prise en charge de l'hypertension artérielle chez la personne âgéeRevue médicale suisse
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2015 522 1
Post-Transcriptional Regulation of Renalase Gene by miR-29 and miR-146 MicroRNAs: Implications for Cardiometabolic DisordersJournal of Molecular Biology
2015 524 0
Genetic studies of body mass index yield new insights for obesity biologyNature
2015 625 0
Associations of ambulatory blood pressure with urinary caffeine and caffeine metabolite excretionsHypertension
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2015 591 1
Inactive Matrix Gla-Protein Is Associated With Arterial Stiffness in an Adult Population-Based StudyHypertension
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2015 515 0
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction StudyPLOS genetics
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2015 516 410
P < 5 × 10(-8) has emerged as a standard of statistical significance for genome-wide association studiesJournal of clinical epidemiology
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2015 387 0
Heritability of ambulatory and office blood pressure in the Swiss populationJournal of hypertension
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2015 593 344
Mon patient est trop âgé pour une statine : mythes et réalitésRevue médicale suisse
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2015 471 0
Directional dominance on stature and cognition in diverse human populationsNature
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2015 557 224
Defining the role of common variation in the genomic and biological architecture of adult human heightNature genetics
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2014 499 0
Genetic evidence for a normal-weight "metabolically obese" phenotype linking insulin resistance, hypertension, coronary artery disease and type 2 diabetesDiabetes
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2014 728 0
Reference values and factors associated with renal resistive index in a family-based population studyHypertension
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2014 914 0
Eligibility for renal denervation: experience at 11 European expert centersHypertension
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2014 687 0
Epidemiology of masked and white-coat hypertension: the family-based SKIPOGH studyPloS one
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2014 688 292
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 studyPloS one
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2014 508 186
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass IndexPLOS genetics
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2014 747 1,245
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associationsAmerican journal of human genetics
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2014 639 3
Predicting stroke through genetic risk functions: the CHARGE Risk Score ProjectStroke
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2014 625 1
Genetic implication of a novel thiamine transporter in human hypertensionJournal of the American College of Cardiology
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2014 503 1
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationNature genetics
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2014 600 1
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP ConsortiaAmerican journal of human genetics
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2014 638 2
Meeting highlights from the 2013 European Society of Cardiology Heart Failure Association Winter Meeting on Translational Heart Failure ResearchEuropean journal of heart failure
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2014 523 0
Discovery and refinement of loci associated with lipid levelsNature genetics
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2013 669 0
Loci influencing blood pressure identified using a cardiovascular gene-centric arrayHuman molecular genetics
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2013 636 496
La génomique cardiovasculaire: l'exemple de l'hypertension artérielle
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2013 640 8
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populationsAmerican journal of human genetics
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2013 625 3
Fine Mapping and Identification of BMI Loci in African AmericansAmerican journal of human genetics
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2013 600 1
Influence of CYP2D6 activity on pre-emptive analgesia by the N-methyl-D-aspartate antagonist dextromethorphan in a randomized controlled trial of acute painPain physician
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2013 789 684
Heritability, determinants and reference values of renal length: a family-based population studyEuropean radiology
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2013 629 0
The Contribution of the Framingham Heart Study to Gene Identification for Cardiovascular Risk Factors and Coronary Heart DiseaseGlobal heart
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2013 545 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) studyPLOS genetics
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2013 662 290
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 studiesCirculation research
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2013 587 0
Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expressionNature medicine
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2013 748 0
Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertensionHuman molecular genetics
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2012 849 2
Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequencyPLoS computational biology
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2012 674 310
Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndromeCirculation. Cardiovascular genetics
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2012 531 454
Genome-wide profiling of blood pressure in adults and childrenHypertension
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2012 676 500
Curing by Burning: What to expect from renal denervation in the treatment of arterial hypertensionKardiovaskuläre Medizin
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2012 610 0
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephronNature genetics
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2012 627 2
A multi-SNP locus-association method reveals a substantial fraction of the missing heritabilityAmerican journal of human genetics
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2012 687 0
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressureNature genetics
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2011 545 1,126
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individualsPLOS genetics
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2011 663 505
Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individualsHypertension
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2011 763 1,147
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasmaNature genetics
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2011 661 999
Genetic variants in novel pathways influence blood pressure and cardiovascular disease riskNature
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2011 603 674
SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertensionPloS one
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2011 663 247
Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure ProgramAmerican journal of hypertension
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2011 675 951
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource studyHuman molecular genetics
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2011 1,056 1,038
Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populationsActa diabetologica
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2010 646 0
Hypertension arterielle résistanteRevue médicale suisse
2010 558 0
Genome-wide association study of blood pressure and hypertensionNature genetics
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2009 624 1
Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet studyEuropean journal of human genetics
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2009 508 0
Positional identification of variants of Adamts16 linked to inherited hypertensionHuman molecular genetics
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2009 616 0
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryNature genetics
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2009 616 1
Common variants at ten loci modulate the QT interval duration in the QTSCD StudyNature genetics
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2009 614 1
Multiple loci associated with indices of renal function and chronic kidney diseaseNature genetics
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2009 965 2
Multiple loci influence erythrocyte phenotypes in the CHARGE ConsortiumNature genetics
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2009 607 1
Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure ProgramEuropean journal of human genetics
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2008 571 0
Methadone-associated long QT syndrome: improving pharmacotherapy for dependence on illegal opioids and lessons learned for pharmacologyExpert opinion on drug safety
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2007 534 651
Drug-induced long QT syndrome in injection drug users receiving methadone: high frequency in hospitalized patients and risk factorsArchives of internal medicine
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2006 486 384
Systemic allergic reaction and diffuse bone pain after exposure to a preparation of betamethasoneEuropean journal of internal medicine
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2005 440 0
QT interval prolongation in patients on methadone with concomitant drugsJournal of clinical psychopharmacology
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2004 477 0
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