Christopher Newton Cheh


Ontology type: schema:Person     


Person Info

NAME

Christopher

SURNAME

Newton Cheh

Publications in SciGraph latest 50 shown

  • 2018-12 Genome-wide analysis yields new loci associating with aortic valve stenosis in NATURE COMMUNICATIONS
  • 2018-12 Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 in GENOME BIOLOGY
  • 2018-12 Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-09 Multi-ethnic genome-wide association study for atrial fibrillation in NATURE GENETICS
  • 2018-03 Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology in THE PHARMACOGENOMICS JOURNAL
  • 2017-10 Abstracts from the 8th International Conference on cGMP Generators, Effectors and Therapeutic Implications in BMC PHARMACOLOGY AND TOXICOLOGY
  • 2017-06 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation in NATURE GENETICS
  • 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
  • 2016-10 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2014-08 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization in NATURE GENETICS
  • 2014-08 Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics in NATURE METHODS
  • 2014-02 Drug–gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval in THE PHARMACOGENOMICS JOURNAL
  • 2013-11 Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes in NATURE GENETICS
  • 2013-08 What have genome-wide association studies taught us about cGMP and blood pressure regulation? in BMC PHARMACOLOGY AND TOXICOLOGY
  • 2013-08 MicroRNA miR-425 is a negative regulator of atrial natriuretic peptide in BMC PHARMACOLOGY AND TOXICOLOGY
  • 2013-06 Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
  • 2012-05 The Electrocardiographic Early Repolarization Pattern in Athletes in SPORTS MEDICINE
  • 2011-12 Human genetics, natriuretic peptides and hypertension in BMC PHARMACOLOGY
  • 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 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction in NATURE GENETICS
  • 2010-05 Genetic Loci Associated with C-Reactive Protein Levels and Risk Of Coronary Heart Disease in CURRENT CARDIOVASCULAR RISK REPORTS
  • 2010-02 Genome-wide association study of PR interval in NATURE GENETICS
  • 2009-08 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry in NATURE GENETICS
  • 2009-06 Genome-wide association study identifies eight loci associated with blood pressure in NATURE GENETICS
  • 2009-04 Common variants at ten loci influence QT interval duration in the QTGEN Study in NATURE GENETICS
  • 2009-03 Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure in NATURE GENETICS
  • 2009 Genome-Wide Association Study in Humans in CARDIOVASCULAR GENOMICS
  • 2008-11 Genetic variation in the NOS1AP gene is associated with the incidence of diabetes mellitus in users of calcium channel blockers in DIABETOLOGIA
  • 2008-11 Randomized trial of genotype-guided versus standard warfarin dosing in patients initiating oral anticoagulation in CURRENT CARDIOVASCULAR RISK REPORTS
  • 2008-05 Rare independent mutations in renal salt handling genes contribute to blood pressure variation in NATURE GENETICS
  • 2008-02 Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans in NATURE GENETICS
  • 2007-11 Leukotriene inhibition in high-risk genotypes in CURRENT CARDIOVASCULAR RISK REPORTS
  • 2007-09 Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study in BMC MEDICAL GENETICS
  • 2007-09 The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports in BMC MEDICAL GENETICS
  • 2007-09 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study in BMC MEDICAL GENETICS
  • 2007-09 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes in BMC MEDICAL GENETICS
  • 2007-09 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness in BMC MEDICAL GENETICS
  • 2006-06 A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization in NATURE GENETICS
  • 2006-02 Conserved noncoding sequences are selectively constrained and not mutation cold spots in NATURE GENETICS
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