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| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Ischemic brain infarcts, white matter hyperintensities, and cognitive impairment are increased in patients with Atrial Fibrillation | Communications medicine | 2026 | 5 | 7 | |||
| Biomarker and cognitive decline in atrial fibrillation : a prospective cohort study | Scientific reports | 2025 | 42 | 39 | |||
| Innovation pour les patients avec hypertension artérielle | Revue médicale suisse | 2024 | 14 | 14 | |||
| Dysfonction érectile chez le patient hypertendu | Revue médicale suisse | 2024 | 17 | 24 | |||
| Heart rate variability and stroke or systemic embolism in patients with atrial fibrillation | Heart rhythm | 2024 | 58 | 169 | |||
| Host-symbiont interactions in Angomonas deanei include the evolution of a host-derived dynamin ring around the endosymbiont division site | Current biology | 2023 | 92 | 100 | |||
| Mesure automatique et non observée de la pression artérielle : un outil précieux pour le clinicien | Revue médicale suisse | 2023 | 12 | 27 | |||
| Sex differences of vascular brain lesions in patients with atrial fibrillation | Open heart | 2022 | 219 | 98 | |||
| Long-term risk of adverse outcomes according to atrial fibrillation type | Scientific reports | 2022 | 225 | 132 | |||
| Uncovering a Genetic Polymorphism Located in Huntingtin Associated Protein 1 in Modulation of Central Pain Sensitization Signaling Pathways | Frontiers in neuroscience | 2022 | 420 | 220 | |||
| Silent brain infarcts impact on cognitive function in atrial fibrillation | European heart journal | 2022 | 255 | 193 | |||
| Dernières recommandations européennes sur les dyslipidémies | Revue médicale suisse | 2022 | 396 | 1,271 | |||
| Increased glucocorticoid metabolism in diabetic kidney disease | PloS one | 2022 | 107 | 161 | |||
| The international database of central arterial properties for risk stratification : research objectives and baseline characteristics of participants | American journal of hypertension | 2022 | 169 | 129 | |||
| Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals | Communications biology | 2022 | 182 | 70 | |||
| Reduced adrenal stress response in patients on PCSK9 inhibitor therapy | Atherosclerosis | 2021 | 241 | 0 | |||
| Gene regulation contributes to explain the impact of early life socioeconomic disadvantage on adult inflammatory levels in two cohort studies | Scientific reports | 2021 | 259 | 297 | |||
| Heritability and association with distinct genetic loci of erythropoietin levels in the general population | Haematologica | 2021 | 284 | 94 | |||
| Une baisse du cholestérol LDL de longue durée : enfin le silence | Revue médicale suisse | 2021 | 293 | 0 | |||
| Assessment of a strategy combining ambulatory blood pressure, adherence monitoring and a standardised triple therapy in resistant hypertension | Blood pressure | 2021 | 245 | 240 | |||
| 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 study | European heart journal | 2021 | 244 | 0 | |||
| Hypertension and heart failure with preserved ejection fraction: position paper by the European Society of Hypertension | Journal of hypertension | 2021 | 174 | 0 | |||
| Insulin-like growth factor-binding protein 7 and risk of congestive heart failure hospitalization in patients with atrial fibrillation | Heart Rhythm | 2021 | 398 | 0 | |||
| Changes of lipoprotein(a) levels with endogenous steroid hormones | European journal of clinical investigation | 2021 | 308 | 363 | |||
| Sex- and age-specific reference intervals for diagnostic ratios reflecting relative activity of steroidogenic enzymes and pathways in adults | PloS one | 2021 | 286 | 252 | |||
| Ambulatory Blood Pressure in Relation to Plasma and Urinary Manganese | Hypertension | 2020 | 308 | 185 | |||
| Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction | Nature communications | 2020 | 204 | 62 | |||
| Blood Pressure and Brain Lesions in Patients With Atrial Fibrillation | Hypertension | 2020 | 627 | 359 | |||
| Analysis of putative cis-regulatory elements regulating blood pressure variation | Human molecular genetics | 2020 | 195 | 169 | |||
| Feasibility and safety of high-intensity interval training for the rehabilitation of geriatric inpatients (HIITERGY) a pilot randomized study | BMC Geriatrics | 2020 | 292 | 342 | |||
| Measured and Genotyped Differences in Blood Pressure and the Usefulness of Precise Extreme Phenotypes Based on Cardiovascular Magnetic Resonance | Hypertension | 2019 | 268 | 1 | |||
| Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | Nature Communications | 2019 | 392 | 310 | |||
| Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels | Nature Genetics | 2019 | 335 | 217 | |||
| A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure | Human Molecular Genetics | 2019 | 466 | 1 | |||
| Reference intervals for the urinary steroid metabolome: The impact of sex, age, day and night time on human adult steroidogenesis | PLOS ONE | 2019 | 305 | 301 | |||
| Relationships of overt and silent brain lesions with cognitive function in patients with atrial fibrillation | Journal of the American College of Cardiology | 2019 | 452 | 0 | |||
| Renal resistive index is associated with inactive Matrix Gla (γ-carboxyglutamate) protein in an adult population-based study | Journal of the American Heart Association | 2019 | 375 | 166 | |||
| Parathyroid hormone and plasma phosphate are predictors of soluble α-klotho levels in adults of European descent | Journal of Clinical Endocrinology and Metabolism | 2019 | 387 | 204 | |||
| Urinary sex steroid and glucocorticoid hormones are associated with muscle mass and strength in healthy adults | Journal of Clinical Endocrinology and Metabolism | 2019 | 328 | 0 | |||
| A catalog of genetic loci associated with kidney function from analyses of a million individuals | Nature Genetics | 2019 | 359 | 365 | |||
| Association of FMO3 variants with blood pressure in the atherosclerosis risk in communities study | International journal of hypertension | 2019 | 334 | 191 | |||
| Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa | Cell | 2019 | 386 | 1 | |||
| Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 | European Journal of Human Genetics | 2019 | 246 | 147 | |||
| In the Age of Genomics, Is it Still Worth it to Investigate Individual Loci? | Hypertension | 2019 | 315 | 2 | |||
| Complex cardiovascular diseases: the genetics of arterial hypertension | The ESC Textbook of Cardiovascular Medicine | 2019 | 332 | 0 | |||
| PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity | Nature Communications | 2018 | 326 | 252 | |||
| Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI | International Journal of Obesity | 2018 | 428 | 0 | |||
| Genes for Preeclampsia: An Opportunity for Blood Pressure Genomics | Hypertension | 2018 | 299 | 197 | |||
| Uromodulin and Nephron Mass | Clinical Journal of the American Society of Nephrology | 2018 | 466 | 363 | |||
| Associations of Urinary Caffeine and Caffeine Metabolites With Arterial Stiffness in a Large Population-Based Study | Mayo Clinic Proceedings | 2018 | 484 | 1 | |||
| Genetics of Hypertension | Hypertension : A Compandion To Braunwald's Heart Diease | 2018 | 316 | 91 | |||
| Epidemiological and histological findings implicate matrix Gla protein in diastolic left ventricular dysfunction | PLOS ONE | 2018 | 495 | 232 | |||
| Association of 24-Hour Blood Pressure With Urinary Sodium Excretion in Healthy Adults | American Journal of Hypertension | 2018 | 434 | 1 | |||
| Copeptin and insulin resistance: effect modification by age and 11 β-HSD2 activity in a population-based study | Journal of Endocrinological Investigation | 2018 | 522 | 554 | |||
| Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits | Nature Genetics | 2018 | 368 | 0 | |||
| A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure | American Journal of Human Genetics | 2018 | 420 | 322 | |||
| A comprehensive evaluation of the genetic architecture of sudden cardiac arrest | European Heart Journal | 2018 | 293 | 0 | |||
| Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries | PLOS ONE | 2018 | 313 | 432 | |||
| Molecular pathways associated with blood pressure and hexadecanedioate levels | PLOS ONE | 2017 | 334 | 216 | |||
| Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry | Journal of Hypertension | 2017 | 315 | 0 | |||
| Design of the Swiss Atrial Fibrillation Cohort Study (Swiss-AF): structural brain damage and cognitive decline among patients with atrial fibrillation | Swiss Medical Weekly | 2017 | 347 | 308 | |||
| Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles | European Journal of Preventive Cardiology | 2017 | 346 | 157 | |||
| Genetic loci associated with heart rate variability and their effects on cardiac disease risk | Nature Communications | 2017 | 303 | 265 | |||
| Urinary cadmium excretion is associated with increased synthesis of cortico- and sex steroids in a population study | Journal of Clinical Endocrinology and Metabolism | 2017 | 632 | 0 | |||
| Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations | International Journal of Obesity | 2017 | 338 | 0 | |||
| Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney | Hypertension | 2017 | 338 | 0 | |||
| A population-based approach to assess the heritability and distribution of renal handling of electrolytes | Kidney International | 2017 | 631 | 0 | |||
| Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation | Nature Genetics | 2017 | 295 | 0 | |||
| Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes | Journal of the American Society of Nephrology | 2017 | 533 | 1 | |||
| New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals | Circulation: Cardiovascular Genetics | 2017 | 293 | 0 | |||
| Next Steps for Gene Identification in Primary Hypertension Genomics | Hypertension | 2017 | 296 | 150 | |||
| Association Analysis of FOXO3 Longevity Variants With Blood Pressure and Essential Hypertension | American journal of hypertension | 2016 | 478 | 1 | |||
| Relation of 24-hour urinary caffeine and caffeine metabolite excretions with self-reported consumption of coffee and other caffeinated beverages in the general population | Nutrition & Metabolism | 2016 | 1,150 | 221 | |||
| A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease | Science Translational Medicine | 2016 | 304 | 0 | |||
| Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior | Human Molecular Genetics | 2016 | 604 | 0 | |||
| Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function | Nature communications | 2016 | 522 | 600 | |||
| Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans | PLOS ONE | 2016 | 314 | 301 | |||
| The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals | Nature Genetics | 2016 | 352 | 0 | |||
| Sociodemographic, behavioral and genetic determinants of allostatic load in a Swiss population-based study | Psychoneuroendocrinology | 2016 | 1,141 | 675 | |||
| The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility | Scientific Reports | 2016 | 304 | 195 | |||
| Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes | Diabetes | 2016 | 549 | 310 | |||
| CYP17A1 Enzyme Activity Is Linked to Ambulatory Blood Pressure in a Family-Based Population Study | American journal of hypertension | 2016 | 551 | 1 | |||
| Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci | Nature Genetics | 2016 | 337 | 0 | |||
| Associations of Urinary Uromodulin with Clinical Characteristics and Markers of Tubular Function in the General Population | Clinical journal of the American Society of Nephrology | 2016 | 673 | 528 | |||
| Fibroblast growth factor 23 and markers of mineral metabolism in individuals with preserved renal function | Kidney international | 2016 | 620 | 397 | |||
| Protocol of the Swiss Longitudinal Cohort Study (SWICOS) in rural Switzerland | BMJ Open | 2016 | 341 | 129 | |||
| Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease | New England Journal of Medicine | 2016 | 370 | 240 | |||
| Heritability of renal function parameters and electrolyte levels in the swiss population | Journal of hypertension | 2015 | 505 | 1 | |||
| Copeptin is associated with kidney length, renal function, and prevalence of simple cysts in a population-based study | Journal of the American Society of Nephrology | 2015 | 593 | 162 | |||
| Dépistage et prise en charge de l'hypertension artérielle chez la personne âgée | Revue médicale suisse | 2015 | 527 | 1 | |||
| Post-Transcriptional Regulation of Renalase Gene by miR-29 and miR-146 MicroRNAs: Implications for Cardiometabolic Disorders | Journal of Molecular Biology | 2015 | 530 | 0 | |||
| Genetic studies of body mass index yield new insights for obesity biology | Nature | 2015 | 631 | 0 | |||
| Associations of ambulatory blood pressure with urinary caffeine and caffeine metabolite excretions | Hypertension | 2015 | 600 | 1 | |||
| Inactive Matrix Gla-Protein Is Associated With Arterial Stiffness in an Adult Population-Based Study | Hypertension | 2015 | 520 | 0 | |||
| The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study | PLOS genetics | 2015 | 525 | 526 | |||
| P < 5 × 10(-8) has emerged as a standard of statistical significance for genome-wide association studies | Journal of clinical epidemiology | 2015 | 394 | 0 | |||
| Heritability of ambulatory and office blood pressure in the Swiss population | Journal of hypertension | 2015 | 604 | 377 | |||
| Mon patient est trop âgé pour une statine : mythes et réalités | Revue médicale suisse | 2015 | 480 | 0 | |||
| Directional dominance on stature and cognition in diverse human populations | Nature | 2015 | 568 | 243 | |||
| Defining the role of common variation in the genomic and biological architecture of adult human height | Nature genetics | 2014 | 506 | 0 | |||
| Genetic evidence for a normal-weight "metabolically obese" phenotype linking insulin resistance, hypertension, coronary artery disease and type 2 diabetes | Diabetes | 2014 | 738 | 0 | |||
| Reference values and factors associated with renal resistive index in a family-based population study | Hypertension | 2014 | 921 | 0 | |||
| Eligibility for renal denervation: experience at 11 European expert centers | Hypertension | 2014 | 699 | 0 | |||
| Epidemiology of masked and white-coat hypertension: the family-based SKIPOGH study | PloS one | 2014 | 696 | 338 | |||
| 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 | PloS one | 2014 | 516 | 225 | |||
| Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index | PLOS genetics | 2014 | 754 | 1,291 | |||
| Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations | American journal of human genetics | 2014 | 645 | 3 | |||
| Predicting stroke through genetic risk functions: the CHARGE Risk Score Project | Stroke | 2014 | 633 | 1 | |||
| Genetic implication of a novel thiamine transporter in human hypertension | Journal of the American College of Cardiology | 2014 | 507 | 1 | |||
| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | Nature genetics | 2014 | 606 | 1 | |||
| Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia | American journal of human genetics | 2014 | 643 | 2 | |||
| Meeting highlights from the 2013 European Society of Cardiology Heart Failure Association Winter Meeting on Translational Heart Failure Research | European journal of heart failure | 2014 | 529 | 0 | |||
| Discovery and refinement of loci associated with lipid levels | Nature genetics | 2013 | 679 | 0 | |||
| Loci influencing blood pressure identified using a cardiovascular gene-centric array | Human molecular genetics | 2013 | 642 | 514 | |||
| La génomique cardiovasculaire: l'exemple de l'hypertension artérielle | 2013 | 649 | 8 | ||||
| Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations | American journal of human genetics | 2013 | 640 | 3 | |||
| Fine Mapping and Identification of BMI Loci in African Americans | American journal of human genetics | 2013 | 612 | 1 | |||
| Influence of CYP2D6 activity on pre-emptive analgesia by the N-methyl-D-aspartate antagonist dextromethorphan in a randomized controlled trial of acute pain | Pain physician | 2013 | 801 | 774 | |||
| Heritability, determinants and reference values of renal length: a family-based population study | European radiology | 2013 | 641 | 0 | |||
| The Contribution of the Framingham Heart Study to Gene Identification for Cardiovascular Risk Factors and Coronary Heart Disease | Global heart | 2013 | 556 | 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 | PLOS genetics | 2013 | 668 | 323 | |||
| 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 | Circulation research | 2013 | 598 | 0 | |||
| Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression | Nature medicine | 2013 | 756 | 0 | |||
| Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension | Human molecular genetics | 2012 | 854 | 2 | |||
| Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency | PLoS computational biology | 2012 | 681 | 362 | |||
| Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome | Circulation. Cardiovascular genetics | 2012 | 548 | 510 | |||
| Genome-wide profiling of blood pressure in adults and children | Hypertension | 2012 | 682 | 518 | |||
| Curing by Burning: What to expect from renal denervation in the treatment of arterial hypertension | Kardiovaskuläre Medizin | 2012 | 619 | 0 | |||
| KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron | Nature genetics | 2012 | 643 | 2 | |||
| A multi-SNP locus-association method reveals a substantial fraction of the missing heritability | American journal of human genetics | 2012 | 693 | 0 | |||
| Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure | Nature genetics | 2011 | 550 | 1,266 | |||
| Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals | PLOS genetics | 2011 | 674 | 537 | |||
| Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals | Hypertension | 2011 | 770 | 1,291 | |||
| Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma | Nature genetics | 2011 | 671 | 1,149 | |||
| Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | Nature | 2011 | 619 | 835 | |||
| SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension | PloS one | 2011 | 671 | 281 | |||
| Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program | American journal of hypertension | 2011 | 683 | 1,019 | |||
| Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study | Human molecular genetics | 2011 | 1,063 | 1,109 | |||
| Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations | Acta diabetologica | 2010 | 656 | 0 | |||
| Hypertension arterielle résistante | Revue médicale suisse | 2010 | 565 | 0 | |||
| Genome-wide association study of blood pressure and hypertension | Nature genetics | 2009 | 635 | 1 | |||
| Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study | European journal of human genetics | 2009 | 519 | 0 | |||
| Positional identification of variants of Adamts16 linked to inherited hypertension | Human molecular genetics | 2009 | 624 | 0 | |||
| Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry | Nature genetics | 2009 | 625 | 1 | |||
| Common variants at ten loci modulate the QT interval duration in the QTSCD Study | Nature genetics | 2009 | 623 | 1 | |||
| Multiple loci associated with indices of renal function and chronic kidney disease | Nature genetics | 2009 | 974 | 2 | |||
| Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium | Nature genetics | 2009 | 625 | 1 | |||
| Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program | European journal of human genetics | 2008 | 580 | 0 | |||
| Methadone-associated long QT syndrome: improving pharmacotherapy for dependence on illegal opioids and lessons learned for pharmacology | Expert opinion on drug safety | 2007 | 542 | 863 | |||
| Drug-induced long QT syndrome in injection drug users receiving methadone: high frequency in hospitalized patients and risk factors | Archives of internal medicine | 2006 | 493 | 478 | |||
| Systemic allergic reaction and diffuse bone pain after exposure to a preparation of betamethasone | European journal of internal medicine | 2005 | 445 | 0 | |||
| QT interval prolongation in patients on methadone with concomitant drugs | Journal of clinical psychopharmacology | 2004 | 485 | 0 |
