Author details

Full Name

Krishna G Aragam

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37429843	Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure.	Nat Commun	2023
37814896	Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research.	Circ Genom Precis Med	2023
37414900	A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.	Nat Med	2023
36576811	Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.	JAMA Cardiol	2023
37451603	Truncations of Titin and Left Atrial Cardiomyopathy: Comment on Henkens et al.'s article, Left Atrial Function in Patients With Titin Cardiomyopathy.		2023
36944631	Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.	Nat Commun	2023
37308786	Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.	Nat Genet	2023
35103786	Identifying Dilated Cardiomyopathy Through Family-Based Screening.	JAMA - Journal of the American Medical Association	2022
36376295	Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.	Nat Commun	2022
35583889	Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank.	JAMA Cardiol	2022
35383479	Genetic Association of Body Mass Index With Pathologic Left Ventricular Remodeling.	J Am Heart Assoc	2022
35818546	Leveraging Population Genomics to Enhance Preventive Cardio-Oncology.	JACC: CardioOncology	2022
36147540	Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease.	JACC Adv	2022
35544052	Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality.	JAMA Cardiol	2022
35294538	Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease.	JAMA Netw Open	2022
34480422	The genomics of heart failure: design and rationale of the HERMES consortium.	ESC Heart Fail	2021
33631942	Lipoprotein(a) and Coronary Artery Disease Risk Without a Family History of Heart Disease.	Journal of the American Heart Association	2021
33893285	The impact of non-additive genetic associations on age-related complex diseases.	Nat Commun	2021
33846329	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.	Nat Commun	2021
33822779	Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.	PLoS Genet	2021
33976420	Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test.	Genet Med	2021
33284643	Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease.	Circ Genom Precis Med	2021
34404223	Predictors of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Inhibitor Prescriptions for Secondary Prevention of Clinical Atherosclerotic Cardiovascular Disease.	Circ Cardiovasc Qual Outcomes	2021
32498804	Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease.	J Am Coll Cardiol	2020
32324503	Polygenic Scores to Assess Atherosclerotic Cardiovascular Disease Risk: Clinical Perspectives and Basic Implications.	Circulation Research	2020
32164899	Titin Truncating Variants in Adults Without Known Congestive HeartÂ Failure.	J Am Coll Cardiol	2020
32382064	Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.	Nat Commun	2020
32827459	Menopausal age and left ventricular remodeling by cardiac magnetic resonance imaging among 14,550 women.	American Heart Journal	2020
32804569	Genetic Variation in Cardiometabolic Traits and Medication Targets and the Risk of Hypertensive Disorders of Pregnancy.	Circulation	2020
33021622	Clinical Utility of Lipoprotein(a) and LPA Genetic Risk Score in Risk Prediction of Incident Atherosclerotic Cardiovascular Disease.	JAMA Cardiology	2020
32957805	Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease.	Arterioscler Thromb Vasc Biol	2020
32616758	An expanded repertoire of intensity-dependent exercise-responsive plasma proteins tied to loci of human disease risk.	Scientific Reports	2020
31549875	Response by Aragam et al to Letter Regarding Article, "Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery".	Circulation	2019
31738818	Association of Premature Natural and Surgical Menopause With Incident Cardiovascular Disease.	JAMA	2019
31727424	Long-Term Cardiovascular Risk inÂ WomenÂ With Hypertension DuringÂ Pregnancy.	J Am Coll Cardiol	2019
30389748	DNA Sequence Variation in <i>ACVR1C</i> Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes.	Diabetes	2019
30615301	Cardiometabolic Polygenic Risk Scores and Osteoarthritis Outcomes: A Mendelian Randomization Study Using Data From the MalmÃ¶ Diet and Cancer Study and the UK Biobank.	Arthritis and Rheumatology	2019
31285632	Genome-wide association study of peripheral artery disease in the Million Veteran Program.	Nat Med	2019
31488267	Sleep Duration and Myocardial Infarction.	J Am Coll Cardiol	2019
31070453	Genetic Association of Finger Photoplethysmography-Derived Arterial Stiffness Index With Blood Pressure and Coronary Artery Disease.	Arterioscler Thromb Vasc Biol	2019
31002795	Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood.	Cell	2019
29691411	Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.	Nat Commun	2018
28982690	Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling.	Circulation	2018
29892015	Multi-ethnic genome-wide association study for atrial fibrillation.	Nat Genet	2018
30220432	Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure.	Am J Hum Genet	2018
30104762	Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.	Nat Genet	2018
29344383	Prognosis of patients with secondary mitral regurgitation and reduced ejection fraction.	Open Heart	2018
29021269	Road Map to Improving Enrollment in Cardiac Rehabilitation: Identifying Barriers and Evaluating Alternatives.	Journal of the American Heart Association	2017
28935042	Preparing Fellows for Precision Cardiology: Are We Ready?	Journal of the American College of Cardiology	2017
25975470	Gaps in referral to cardiac rehabilitation of patients undergoing percutaneous coronary intervention in the United States.	J Am Coll Cardiol	2015