Georg Ehret


Ontology type: schema:Person     


Person Info

NAME

Georg

SURNAME

Ehret

Publications in SciGraph latest 50 shown

  • 2019-02 Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-12 Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-12 PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity in NATURE COMMUNICATIONS
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-07 Copeptin and insulin resistance: effect modification by age and 11 β-HSD2 activity in a population-based study in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2017-06 Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci in HUMAN GENETICS
  • 2017-02 Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations in INTERNATIONAL JOURNAL OF OBESITY
  • 2017-01 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation in NATURE GENETICS
  • 2016-12 The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility in SCIENTIFIC REPORTS
  • 2016-12 Relation of 24-hour urinary caffeine and caffeine metabolite excretions with self-reported consumption of coffee and other caffeinated beverages in the general population in NUTRITION & METABOLISM
  • 2016-10 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci in NATURE GENETICS
  • 2016-10 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2015-07-01 Directional dominance on stature and cognition in diverse human populations in NATURE
  • 2015-02 Genetic studies of body mass index yield new insights for obesity biology in NATURE
  • 2015-02 New genetic loci link adipose and insulin biology to body fat distribution in NATURE
  • 2015 Blood Pressure Genomics in PATHOPHYSIOLOGY AND PHARMACOTHERAPY OF CARDIOVASCULAR DISEASE
  • 2014-11 Defining the role of common variation in the genomic and biological architecture of adult human height in NATURE GENETICS
  • 2014-08 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization in NATURE GENETICS
  • 2013-11 Common variants associated with plasma triglycerides and risk for coronary artery disease in NATURE GENETICS
  • 2013-11 Discovery and refinement of loci associated with lipid levels in NATURE GENETICS
  • 2013-10 Heritability, determinants and reference values of renal length: a family-based population study in EUROPEAN RADIOLOGY
  • 2012-04 KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron in NATURE GENETICS
  • 2011-11 Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma in NATURE GENETICS
  • 2011-10 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk in NATURE
  • 2011-10 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure in NATURE GENETICS
  • 2010-12 Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations in ACTA DIABETOLOGICA
  • 2010-03 Common variants in KCNN3 are associated with lone atrial fibrillation in NATURE GENETICS
  • 2010-02 Genome-Wide Association Studies: Contribution of Genomics to Understanding Blood Pressure and Essential Hypertension in CURRENT HYPERTENSION REPORTS
  • 2010-02 Genome-wide association study of PR interval in NATURE GENETICS
  • 2009-12 Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium in NATURE GENETICS
  • 2009-08 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry in NATURE GENETICS
  • 2008-12 Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2003-02 Methadone and QT interval in CLINICAL PHARMACOLOGY & THERAPEUTICS
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