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Author Details

Patrick T Ellinor
Cardiovascular Research Center, Massachusetts General Hospital
1989
445
94
PMIDPaper TitleJournal TitlePublished Year
38095107Using Genomics to Identify Novel Therapeutic Targets for Aortic Disease.Arterioscler Thromb Vasc Biol2024
37950744Natural Language Processing for Adjudication of Heart Failure in a Multicenter Clinical Trial: A Secondary Analysis of a Randomized Clinical Trial.JAMA Cardiol2024
38095107Using Genomics to Identify Novel Therapeutic Targets for Aortic Disease.Arterioscler Thromb Vasc Biol2024
37798122Deep learned representations of the resting 12-lead electrocardiogram to predict at peak exercise.Eur J Prev Cardiol2024
37694688Genetically predicted gestational age and birth weight are associated with cardiac and pulmonary vascular remodelling in adulthood.Eur J Prev Cardiol2024
37952204Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias.Eur Heart J2024
37798122Deep learned representations of the resting 12-lead electrocardiogram to predict at peak exercise.Eur J Prev Cardiol2024
37952204Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias.Eur Heart J2024
37950744Natural Language Processing for Adjudication of Heart Failure in a Multicenter Clinical Trial: A Secondary Analysis of a Randomized Clinical Trial.JAMA Cardiol2024
37694688Genetically predicted gestational age and birth weight are associated with cardiac and pulmonary vascular remodelling in adulthood.Eur J Prev Cardiol2024
35980763A polygenic risk score predicts atrial fibrillation in cardiovascular disease.Eur Heart J2023
36131050Genetics and mechanisms of thoracic aortic disease.Nat Rev Cardiol2023
35980763A polygenic risk score predicts atrial fibrillation in cardiovascular disease.Eur Heart J2023
37609134Characteristics and Attitudes of Wearable Device Users and Non-Users in a Large Healthcare System.medRxiv2023
38042913Selenoprotein deficiency disorder predisposes to aortic aneurysm formation.Nat Commun2023
37852978Clinical utility of polygenic scores for cardiometabolic disease in Arabs.Nat Commun2023
38033629Treatment of calcific arterial disease via enhancement of autophagy using GSK343.iScience2023
37940231Deep Learning-Enabled Assessment of Left Heart Structure and Function Predicts Cardiovascular Outcomes.J Am Coll Cardiol2023
37662283Natural Language Processing for Adjudication of Heart Failure Hospitalizations in a Multi-Center Clinical Trial.medRxiv2023
37662232AORTA Gene: Polygenic prediction improves detection of thoracic aortic aneurysm.medRxiv2023
38014050Transcriptional profile of the rat cardiovascular system at single cell resolution.bioRxiv2023
37814896Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research.Circ Genom Precis Med2023
37730292Clinical Pathway for Coronary Atherosclerosis in Patients Without Conventional Modifiable Risk Factors: JACC State-of-the-Art Review.J Am Coll Cardiol2023
37645259Effect of clinic-based single-lead electrocardiogram rhythm assessment on oral anticoagulation prescriptions in patients with previously diagnosed atrial fibrillation.Heart Rhythm O22023
37986972MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record.medRxiv2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37961173Decoding Genetics, Ancestry, and Geospatial Context for Precision Health.medRxiv2023
37958923Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies.Int J Mol Sci2023
37550580Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender.Nat Methods2023
37414900A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.Nat Med2023
37348055Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.Genetics2023
36780164Prevalence and Incidence of Atrial Fibrillation Among Older Primary Care Patients.JAMA Netw Open2023
36972346A Mouse Model of Atrial Fibrillation in Sepsis.Circulation2023
36778406Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.bioRxiv2023
37278238Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms.Circ Genom Precis Med2023
36650173BMI-adjusted adipose tissue volumes exhibit depot-specific and divergent associations with cardiometabolic diseases.Nat Commun2023
37205587Assessment of valvular function in over 47,000 people using deep learning-based flow measurements.medRxiv2023
37144117Atrial Fibrillation in Patients With Cancer: A Persistent and Increasing Challenge.JACC CardioOncol2023
37081215Genetics of myocardial interstitial fibrosis in the human heart and association with disease.Nat Genet2023
36959364Adjusting for common variant polygenic scores improves yield in rare variant association analyses.Nat Genet2023
36580284Machine Learning to Understand Genetic and Clinical Factors Associated With the Pulse Waveform Dicrotic Notch.Circ Genom Precis Med2023
36576811Predictive Utility of a Coronary Artery Disease Polygenic Risk Score in Primary Prevention.JAMA Cardiol2023
37462704Accelerometer-Derived "Weekend Warrior" Physical Activity and Incident Cardiovascular Disease.JAMA2023
37079300Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.JAMA Ophthalmol2023
37019578The Genetic Determinants of Aortic Distention.J Am Coll Cardiol2023
37264683Association of genetic risk and outcomes in patients with atrial fibrillation: interactions with early rhythm control in the EAST-AFNET4 trial.Cardiovasc Res2023
37199186Genetic Burden of <i>TNNI3K</i> in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias.Circ Genom Precis Med2023
37072623Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program.J Hum Genet2023
37391738Screening for undiagnosed atrial fibrillation using a single-lead electrocardiogram at primary care visits: patient uptake and practitioner perspectives from the VITAL-AF trial.BMC Prim Care2023
37451355Accuracy and variability of cardiologist interpretation of single lead electrocardiograms for atrial fibrillation: The VITAL-AF trial.Am Heart J2023
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Collaborators

Steven A Lubitz
Cardiovascular Research Center, Massachusetts General Hospital
Co-authored papers 207
Emelia J Benjamin
Co-authored papers 131
Susan R Heckbert
Co-authored papers 54
Honghuang Lin
Co-authored papers 51
Alvaro Alonso
Rollins School of Public Health, Emory University
Co-authored papers 48
Bruce M Psaty
Co-authored papers 47
Kathryn L Lunetta
Co-authored papers 47
Ramachandran S Vasan
Co-authored papers 46
Jerome I Rotter
Co-authored papers 43
Nona Sotoodehnia
Johns Hopkins University School of Medicine
Co-authored papers 40
Dan E Arking
Co-authored papers 37
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 37
Joshua C Bis
Co-authored papers 36
Nathan R Tucker
Co-authored papers 35
James P Pirruccello
Co-authored papers 35
Martina M??ller-Nurasyid
Institute for Medical Information Processing
Co-authored papers 33
Daniel Levy
and Blood Institute, National Institutes of Health
Co-authored papers 33
Calum A MacRae
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
Co-authored papers 33
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 32
Charles Kooperberg
Co-authored papers 32
Mark Chaffin
Co-authored papers 32
Seung Hoan Choi
Broad Institute of MIT and Harvard
Co-authored papers 32
Sekar Kathiresan
Co-authored papers 31
Carolina Roselli
Co-authored papers 31
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 30
Christopher Newton-Cheh
Co-authored papers 30
Martin G Larson
Co-authored papers 29
Anthony A Philippakis
Broad Institute of Harvard and the Massachusetts Institute of Technology
Co-authored papers 28
Xiuqing Guo
Co-authored papers 27
Kent D Taylor
Co-authored papers 27
Release 1.2