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Author Details

Seung Hoan Choi
Broad Institute of MIT and Harvard
2009
64
30
PMIDPaper TitleJournal TitlePublished Year
36334690Systematic dissection, preservation, and multiomics in whole human and bovine hearts.Cardiovasc Pathol2023
36334690Systematic dissection, preservation, and multiomics in whole human and bovine hearts.Cardiovasc Pathol2023
37693521Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project.medRxiv2023
37693453Key variants via Alzheimer's Disease Sequencing Project whole genome sequence data.medRxiv2023
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
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
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
36944631Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.Nat Commun2023
37693521Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project.medRxiv2023
37693453Key variants via Alzheimer's Disease Sequencing Project whole genome sequence data.medRxiv2023
37019578The Genetic Determinants of Aortic Distention.J Am Coll Cardiol2023
37081215Genetics of myocardial interstitial fibrosis in the human heart and association with disease.Nat Genet2023
37079300Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.JAMA Ophthalmol2023
36944631Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.Nat Commun2023
37072623Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program.J Hum Genet2023
37199186Genetic Burden of <i>TNNI3K</i> in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias.Circ Genom Precis Med2023
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
35902171Spatially Distinct Genetic Determinants of Aortic Dimensions Influence Risks of Aneurysm and Stenosis.J Am Coll Cardiol2022
35772917LMNA Variants and Risk of Adult-Onset Cardiac Disease.J Am Coll Cardiol2022
36180445Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.Nat Commun2022
36042188Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.Nat Commun2022
35902171Spatially Distinct Genetic Determinants of Aortic Dimensions Influence Risks of Aneurysm and Stenosis.J Am Coll Cardiol2022
35389749Monogenic and Polygenic Contributions to QTc Prolongation in the Population.Circulation2022
35583889Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank.JAMA Cardiol2022
35772917LMNA Variants and Risk of Adult-Onset Cardiac Disease.J Am Coll Cardiol2022
35583889Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank.JAMA Cardiol2022
35389749Monogenic and Polygenic Contributions to QTc Prolongation in the Population.Circulation2022
36180445Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.Nat Commun2022
36042188Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.Nat Commun2022
34319147Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.Circ Genom Precis Med2021
33792063Multi-omics analyses implicate EARS2 in the pathogenesis of atopic dermatitis.Allergy2021
34319147Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.Circ Genom Precis Med2021
33792063Multi-omics analyses implicate EARS2 in the pathogenesis of atopic dermatitis.Allergy2021
32164899Titin Truncating Variants in Adults Without Known Congestive Heart Failure.J Am Coll Cardiol2020
32078361Initial Precipitants and Recurrence of Atrial Fibrillation.Circ Arrhythm Electrophysiol2020
31691645Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank.Circ Res2020
32403949Transcriptional and Cellular Diversity of the Human Heart.Circulation2020
32164899Titin Truncating Variants in Adults Without Known Congestive Heart Failure.J Am Coll Cardiol2020
32439900Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.Nat Commun2020
33156697Associations Between Alcohol Intake and Genetic Predisposition With Atrial Fibrillation Risk in a National Biobank.Circ Genom Precis Med2020
32822252Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.Circ Genom Precis Med2020
33339817Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.Nat Commun2020
33067605Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.Nat Metab2020
32078361Initial Precipitants and Recurrence of Atrial Fibrillation.Circ Arrhythm Electrophysiol2020
31691645Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank.Circ Res2020
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Collaborators

Patrick T Ellinor
Cardiovascular Research Center, Massachusetts General Hospital
Co-authored papers 32
Steven A Lubitz
Cardiovascular Research Center, Massachusetts General Hospital
Co-authored papers 31
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 23
Bruce M Psaty
Co-authored papers 22
Kathryn L Lunetta
Co-authored papers 22
Joshua C Bis
Co-authored papers 22
Cornelia M van Duijn
University of Oxford
Co-authored papers 18
Lenore J Launer
Co-authored papers 17
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 16
Jerome I Rotter
Co-authored papers 16
Emelia J Benjamin
Co-authored papers 16
Vilmundur Gudnason
Co-authored papers 15
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers 14
Honghuang Lin
Co-authored papers 14
Mark Chaffin
Co-authored papers 13
Jennifer A Brody
Co-authored papers 12
Susan R Heckbert
Co-authored papers 12
Gerard D Schellenberg
Co-authored papers 11
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 11
James P Pirruccello
Co-authored papers 11
Najaf Amin
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Carolina Roselli
Co-authored papers 11
Lindsay A Farrer
Boston University Chobanian & Avedisian School of Medicine
Co-authored papers 10
Charles Kooperberg
Co-authored papers 10
Philip L De Jager
Columbia University Medical Center
Co-authored papers 10
Myriam Fornage
Co-authored papers 10
Nona Sotoodehnia
Johns Hopkins University School of Medicine
Co-authored papers 10
Oscar L Lopez
University of Pittsburgh
Co-authored papers 9
Sekar Kathiresan
Co-authored papers 9
Thomas H Mosley
Co-authored papers 9
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