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Author Details

Christopher Newton-Cheh
2004
218
78
PMIDPaper TitleJournal TitlePublished Year
34616002A NOS1AP gene variant is associated with a paradoxical increase of the QT-interval shortening effect of digoxin.Pharmacogenomics J2022
36175050Hemodynamic and Clinical Performance of Hearts Donated After Circulatory Death.Journal of the American College of Cardiology2022
36073647Heart Failure Strategically Focused Research Network: Summary of Results and Future Directions.J Am Heart Assoc2022
36260795Case 32-2022: A 76-Year-Old Man with Postoperative Cardiogenic Shock and Diffuse Rash.N Engl J Med2022
35473782Sex-Specific Differences in Ventricular Remodeling and Response After Cardiac Resynchronization Therapy.Am J Cardiol2022
36050321Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.Nat Commun2022
34849680Multisystem Inflammatory Syndrome in Adults After Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Coronavirus Disease 2019 (COVID-19) Vaccination.Clin Infect Dis2022
34480422The genomics of heart failure: design and rationale of the HERMES consortium.ESC Heart Fail2021
33960201Effects of Vitamin D Supplementation on Cardiovascular and Glycemic Biomarkers.J Am Heart Assoc2021
33727701Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2021
33727695Factors associated with myocardial SARS-CoV-2 infection, myocarditis, and cardiac inflammation in patients with COVID-19.Modern Pathology2021
34095452Virtual multidisciplinary care for heart failure patients with cardiac resynchronization therapy devices during the Coronavirus Disease 2019 pandemic.IJC Heart and Vasculature2021
33283203Elevated Blood Pressure Increases Pneumonia Risk: Epidemiological Association and Mendelian Randomization in the UK Biobank.Med2021
32668103Case 24-2020: A 44-Year-Old Woman with Chest Pain, Dyspnea, and Shock.N Engl J Med2020
32429735Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.Circulation2020
31707834Multicenter Analysis of Dosing Protocols for Sotalol Initiation.J Cardiovasc Pharmacol Ther2020
32439900Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.Nat Commun2020
33031361Case Series of Multisystem Inflammatory Syndrome in Adults Associated with SARS-CoV-2 Infection - United Kingdom and United States, March-August 2020.Morbidity and Mortality Weekly Report2020
33230300Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2020
31296288Pathogenic TSR1 Gene Variants in Patients With Spontaneous Coronary Artery Dissection.Journal of the American College of Cardiology2019
31891645Applications of machine learning in decision analysis for dose management for dofetilide.PLoS One2019
31727422Rare Genetic Variants Associated With Sudden Cardiac Death in Adults.J Am Coll Cardiol2019
31221261Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals.J Am Coll Cardiol2019
31430210Blood Pressure-Associated Genetic Variants in the Natriuretic Peptide Receptor 1 Gene Modulate Guanylate Cyclase Activity.Circulation. Genomic and precision medicine2019
31353243Pre-emptive pangenotypic direct acting antiviral therapy in donor HCV-positive to recipient HCV-negative heart transplantation: an open-label study.Lancet Gastroenterol Hepatol2019
31196450What Can We Learn From Common Genetic Variants With Weak Effects on Cardiovascular Disease Risk?Journal of the American College of Cardiology2019
29768145Case 15-2018: An 83-Year-Old Woman with Nausea, Vomiting, and Confusion.New England Journal of Medicine2018
28719597Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.Pharmacogenomics J2018
29892015Multi-ethnic genome-wide association study for atrial fibrillation.Nat Genet2018
30169657A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.Eur Heart J2018
30354828Resistant Hypertension: Detection, Evaluation, and Management: A Scientific Statement From the American Heart Association.Hypertension2018
29874175ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.Circ Genom Precis Med2018
30012220Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.Genome Biol2018
30429575Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
30224653Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.Nat Genet2018
29752399Common Coding Variants in <i>SCN10A</i> Are Associated With the Nav1.8 Late Current and Cardiac Conduction.Circ Genom Precis Med2018
29698509MicroRNA-425 and microRNA-155 cooperatively regulate atrial natriuretic peptide expression and cGMP production.PLoS ONE2018
29511194Genome-wide analysis yields new loci associating with aortic valve stenosis.Nat Commun2018
29540468Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects.Circ Genom Precis Med2018
28135244Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.Nat Genet2017
28951623Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.Nat Genet2017
28986454Validation of Polygenic Scores for QT Interval in Clinical Populations.Circ Cardiovasc Genet2017
28760750The Expressed Genome in Cardiovascular Diseases and Stroke: Refinement, Diagnosis, and Prediction: A Scientific Statement From the American Heart Association.Circ Cardiovasc Genet2017
28416818Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
28747752Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
28739976Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.Hypertension2017
29030403New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475â¿¿000 Individuals.Circ Cardiovasc Genet2017
29073956Should Identifying a Titin Truncating Variant Change the Management of Patients With Dilated Cardiomyopathy?Journal of the American College of Cardiology2017
29237688Heritability of Atrial Fibrillation.Circ Cardiovasc Genet2017
27894865The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study.J Mol Cell Cardiol2017
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