Seung Hoan Choi

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

8.5Author DataRank

Indexed papers

4in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 4 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 57 papers — median percentile 61. Top paper: “Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals”.

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

Nature Metabolism(2020)10.1038/s42255-020-00287-2

N/A

10.0DataRank · unranked

782 citations

Stefan Gustafsson, Qin Wang, Daniel Hvidberg Hansen, Åsa K. Hedman, Andrew J. Schork +78 more

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00935-7

N/A

4.0DataRank · unranked

191 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Titin Truncating Variants in Adults Without Known Congestive Heart Failure

Journal of the American College of Cardiology(2020)10.1016/j.jacc.2020.01.013

N/A

1.6DataRank · unranked

28 citations

Alexander G. Bick, Mark Chaffin, Krishna G. Aragam, Seung Hoan Choi, Steven A. Lubitz +7 more

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 more

Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002874

N/A

1.4DataRank · unranked

30 citations

Amelia Weber Hall, Seung Hoan Choi, Sean J. Jurgens, Jeffrey Haessler, Nathan A. Bihlmeyer +55 more

Noninvasive assessment of organ-specific and shared pathways in multi-organ fibrosis using T1 mapping

Nature Medicine(2024)10.1038/s41591-024-03010-w

N/A

1.2DataRank · unranked

36 citations

Marcus D. R. Klarqvist, Matthew C. Hill, Danielle F. Pace, Paolo Di Achille, Seung Hoan Choi +11 more

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Nature Communications(2022)10.1038/s41467-022-32275-3

N/A

1.1DataRank · unranked

63 citations

Daniel H. Katz, Julián Ávila-Pacheco, Alexander G. Bick, Akhil Pampana, Jeremy Robbins +95 more

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Genome Medicine(2021)10.1186/s13073-021-00917-8

Top 21%

0.976DataRank

Top 21%35 citations

Jiwon Lee, Tamar Sofer, Heming Wang, Man Zhang, Han Chen +94 more

Deep learning of left atrial structure and function provides link to atrial fibrillation risk

Nature Communications(2024)10.1038/s41467-024-48229-w

N/A

0.931DataRank · unranked

38 citations

Paolo Di Achille, Seung Hoan Choi, Joel Rämö, Shaan Khurshid, Mahan Nekoui +14 more

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Nature Communications(2021)10.1038/s41467-021-23655-2

N/A

0.840DataRank · unranked

21 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +91 more

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3

N/A

0.821DataRank · unranked

50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +95 more

Rare Genetic Variants in LDLR , APOB , and PCSK9 Are Associated With Aortic Stenosis

Circulation(2024)10.1161/circulationaha.124.070982

N/A

0.741DataRank · unranked

18 citations

Sean J. Jurgens, Shinwan Kany, Seung Hoan Choi, Xin Wang, Andrey N. Smirnov +6 more

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Nature Medicine(2025)10.1038/s41591-025-03827-z

N/A

0.665DataRank · unranked

34 citations

Kaitlin H Wade, Qin Hui, Joshua Arias, Xianyong Yin, Malene R. Christiansen +95 more

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program

Journal of Human Genetics(2023)10.1038/s10038-023-01147-z

N/A

0.549DataRank · unranked

12 citations

Justine Ryu, Jihoon Kim, Andrea H. Ramirez, Kelsey Mayo, Henry Robert Condon +7 more

Rare variant contribution to the heritability of coronary artery disease

Nature Communications(2024)10.1038/s41467-024-52939-6

N/A

0.513DataRank · unranked

16 citations

Shoa L. Clarke, Gaëlle Auguste, Natalie R. Hasbani, Alanna C. Morrison, Adam S. Heath +95 more

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.123.004320

N/A

0.413DataRank · unranked

10 citations

Shaan Khurshid, Amelia Weber Hall, Victor Nauffal, Valerie N. Morrill, Yan V. Sun +54 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

medRxiv(2021)10.1101/2021.06.18.21258578

N/A

0.320DataRank · unranked

5 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia Weber Hall, Lu‐Chen Weng +33 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Key variants via Alzheimer’s Disease Sequencing Project whole genome sequence data

medRxiv(2023)10.1101/2023.08.28.23294631

Top 59%

0.257DataRank

Top 59%4 citations

Chloé Sarnowski, Honghuang Lin, Achilleas Pitsillides, Nancy L. Heard‐Costa, Seung Hoan Choi +14 more

Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00979-9

N/A

0.246DataRank · unranked

4 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

Deep Learning of Electrocardiograms Enables Scalable Human Disease Profiling

medRxiv(2022)10.1101/2022.12.21.22283757

N/A

0.165DataRank · unranked

2 citations

Xin Wang, Sam Friedman, Nate Diamant, Shaan Khurshid, Paolo Di Achille +13 more

Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-lead Electrocardiograms

medRxiv(2022)10.1101/2022.01.17.22269357

N/A

0.149DataRank · unranked

1 citations

Shaan Khurshid, Seung Hoan Choi, Sam Friedman, Lu‐Chen Weng, Christopher Reeder +13 more

Multi-ancestry genome-wide association study reveals novel genetic signals for lung function decline

medRxiv(2024)10.1101/2024.11.25.24317794

N/A

0.104DataRank · unranked

1 citations

Jingwen Zhang, Nathan Gaddis, Traci M. Bartz, Jing Chen, Catherine L. Debban +31 more

Unsupervised deep learning of electrocardiograms enables scalable human disease profiling

npj Digital Medicine(2025)10.1038/s41746-024-01418-9

N/A

0DataRank · unranked

19 citations

Shaan Khurshid, Rachael A. Venn, Xin Wang, Nate Diamant, Paolo Di Achille +14 more

Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma

Nature Communications(2025)10.1038/s41467-025-58686-6

N/A

0DataRank · unranked

11 citations

Bryan R. Gorman, Lu‐Chen Weng, Sean J. Jurgens, Panisa Singhanetr, Marisa G. Tieger +28 more

Association of genetic risk of Alzheimer’s disease and cognitive function in two European populations

Scientific Reports(2025)10.1038/s41598-025-90277-9

N/A

0DataRank · unranked

8 citations

Lori B. Chibnik, Seung Hoan Choi, Deborah Blacker, Anita L. DeStefano, Honghuang Lin +1 more

Population-scale analysis reveals inherited C1-inhibitor deficiency is a polyphenotypic thrombotic disorder

Blood Advances(2025)10.1182/bloodadvances.2025017220

N/A

0DataRank · unranked

2 citations

Amelia K. Haj, Sean J. Jurgens, Harish Eswaran, Linda Sundler Björkman, Justine Ryu +11 more

Multiple-testing corrections in case-control studies using identity-by-descent segments

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.03.663057

N/A

0DataRank · unranked

0 citations

Nicola H. Chapman, Seung Hoan Choi, Anita L. DeStefano, Timothy A. Thornton, Ellen M. Wijsman +2 more

Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses

medRxiv(2023)10.1101/2023.09.24.23295485

N/A

0DataRank · unranked

0 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +56 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

0DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Transcriptional and Cellular Diversity of the Human Heart

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.06.896076

N/A

0DataRank · unranked

54 citations

Mark Chaffin, Stephen J. Fleming, Amelia Weber Hall, Victoria A. Parsons, Kenneth Bedi +13 more

Deep learning enables genetic analysis of the human thoracic aorta

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.12.091934

N/A

0DataRank · unranked

34 citations

Mark Chaffin, Stephen J. Fleming, Alessandro Arduini, Honghuang Lin, Shaan Khurshid +21 more

Genetics of Myocardial Interstitial Fibrosis in the Human Heart and Association with Disease

medRxiv(2021)10.1101/2021.11.05.21265953

N/A

0DataRank · unranked

12 citations

Paolo Di Achille, Marcus D. R. Klarqvist, Jonathan W. Cunningham, James P. Pirruccello, Lu‐Chen Weng +12 more

Deep Learning of Left Atrial Structure and Function Provides Link to Atrial Fibrillation Risk

medRxiv(2021)10.1101/2021.08.02.21261481

N/A

0DataRank · unranked

10 citations

Paolo Di Achille, Seung Hoan Choi, Shaan Khurshid, Mahan Nekoui, Sean J. Jurgens +9 more

Machine Learning to Understand Genetic and Clinical Factors Associated with the Pulse Waveform Dicrotic Notch

medRxiv(2021)10.1101/2021.12.09.21267484

N/A

0DataRank · unranked

4 citations

Paolo Di Achille, Valerie N. Morrill, Lu‐Chen Weng, Seung Hoan Choi, Shaan Khurshid +9 more

A saturated map of common genetic variants associated with human height

Nature(2022)10.1038/s41586-022-05275-y

N/A

0DataRank · unranked

908 citations

Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Saori Sakaue +95 more

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Nature Genetics(2022)10.1038/s41588-021-01007-6

N/A

0DataRank · unranked

143 citations

Rafik Tadros, Charlotte Glinge, David Y. Chiang, Mariam Jouni, Floriane Simonet +95 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

Circulation(2022)10.1161/circulationaha.121.057261

N/A

0DataRank · unranked

50 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia W. Hall, Lu-Chen Weng +34 more

Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

Nature Communications(2022)10.1038/s41467-022-32009-5

N/A

0DataRank · unranked

10 citations

Valerie N. Morrill, Seung Hoan Choi, Sean J. Jurgens, Giorgio Melloni, Nicholas Marston +39 more

Clinical and Genetic Associations of Deep Learning-Derived Cardiac Magnetic Resonance-Based Left Ventricular Mass

medRxiv(2022)10.1101/2022.01.09.22268962

N/A

0DataRank · unranked

1 citations

Julieta Lazarte, James P. Pirruccello, Lu‐Chen Weng, Seung Hoan Choi, Amelia Weber Hall +11 more

Genetics of myocardial interstitial fibrosis in the human heart and association with disease

Nature Genetics(2023)10.1038/s41588-023-01371-5

N/A

0DataRank · unranked

85 citations

Paolo Di Achille, Marcus D. R. Klarqvist, Jonathan W. Cunningham, Matthew C. Hill, James P. Pirruccello +13 more

Adjusting for common variant polygenic scores improves yield in rare variant association analyses

Nature Genetics(2023)10.1038/s41588-023-01342-w

N/A

0DataRank · unranked

46 citations

James P. Pirruccello, Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, Steven A. Lubitz +3 more

Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass

Nature Communications(2023)10.1038/s41467-023-37173-w

N/A

0DataRank · unranked

42 citations

Julieta Lazarte, James P. Pirruccello, Lu‐Chen Weng, Seung Hoan Choi, Amelia Weber Hall +11 more

The Genetic Determinants of Aortic Distention

Journal of the American College of Cardiology(2023)10.1016/j.jacc.2023.01.044

N/A

0DataRank · unranked

35 citations

Joel Rämö, Seung Hoan Choi, Mark Chaffin, Shinwan Kany, Mahan Nekoui +11 more

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

EBioMedicine(2023)10.1016/j.ebiom.2023.104758

N/A

0DataRank · unranked

19 citations

Priyadarshini Kachroo, Tianxiao Huan, David Van Den Berg, Gha Young Lee, Helena Bui +95 more

Rare coding variant analysis for human diseases across biobanks and ancestries

Nature Genetics(2024)10.1038/s41588-024-01894-5

N/A

0DataRank · unranked

58 citations

Xin Wang, Seung Hoan Choi, Lu‐Chen Weng, Satoshi Koyama, James P. Pirruccello +20 more

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Nature Genetics(2024)10.1038/s41588-024-01975-5

N/A

0DataRank · unranked

51 citations

Joel Rämö, Daria R. Kramarenko, Leonoor F. J. M. Wijdeveld, Jan Haas, Mark Chaffin +55 more

Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

Blood(2024)10.1182/blood.2023023326

N/A

0DataRank · unranked

24 citations

Joel Rämö, Sean J. Jurgens, Teemu Niiranen, Simone Sanna‐Cherchi, Kenneth A. Bauer +7 more

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Nature Communications(2024)10.1038/s41467-024-47739-x

N/A

0DataRank · unranked

24 citations

Hiroshige Murata, Fernanda M. Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum +39 more

Lipid levels and risk of acute pancreatitis using bidirectional Mendelian randomization

Scientific Reports(2024)10.1038/s41598-024-56946-x

N/A

0DataRank · unranked

16 citations

Jacqueline S. Dron, Yuxuan Wang, Seung Hoan Choi, Jennifer E. Huffman, Kelly Cho +4 more

Loss of function in protein Z (PROZ) is associated with increased risk of ischemic stroke in the UK Biobank

Journal of Thrombosis and Haemostasis(2024)10.1016/j.jtha.2024.09.016

N/A

0DataRank · unranked

6 citations

Justine Ryu, Sean J. Jurgens, Sharjeel Chaudhry, Satoshi Koyama, Xin Wang +7 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0DataRank · unranked

19 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Seung Hoan Choi

Indexed papers

Top data-sharing exemplar

Papers