Sean J. Jurgens

Also affiliated with Harvard University, Academic Center for Dentistry Amsterdam, Massachusetts General Hospital, Amsterdam Neuroscience, ERN GUARD-Heart, Amsterdam University Medical Centers, Amsterdam University of Applied Sciences, University of Amsterdam

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 38 papers. Top paper: “Genetic analysis of right heart structure and function in 40,000 people”.

Genetic analysis of right heart structure and function in 40,000 people

Nature Genetics(2022)10.1038/s41588-022-01090-3

N/A

2.2DataRank · unranked

99 citations

Paolo Di Achille, Victor Nauffal, Mahan Nekoui, Sam Friedman, Marcus D. R. Klarqvist +46 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

Genetic testing in early-onset atrial fibrillation

European Heart Journal(2024)10.1093/eurheartj/ehae298

N/A

1.1DataRank · unranked

39 citations

Sean J. Jurgens, Joel Rämö, Ingrid E. Christophersen, Michiel Rienstra, Mina K. Chung +14 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

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

Nature Cardiovascular Research(2023)10.1038/s44161-023-00346-3

N/A

0.863DataRank · unranked

34 citations

Sean J. Jurgens, Francesco Mazzarotto, Mona Allouba, James P. Pirruccello, Yasmine Aguib +6 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

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

Selenoprotein deficiency disorder predisposes to aortic aneurysm formation

Nature Communications(2023)10.1038/s41467-023-43851-6

N/A

0.483DataRank · unranked

24 citations

Federica Marelli, Helle F. Jørgensen, W. Edward Visser, Carla Moran, Stefan Groeneweg +26 more

The impact of common and rare genetic variants on bradyarrhythmia development

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

N/A

0.464DataRank · unranked

21 citations

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

Assessment of valvular function in over 47,000 people using deep learning-based flow measurements

medRxiv(2023)10.1101/2023.04.29.23289299

N/A

0.165DataRank · unranked

2 citations

Cody Hou, Sean J. Jurgens, Victor Nauffal, Jon Cunningham, Emily S. Lau +12 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

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

medRxiv(2023)10.1101/2023.01.28.23285147

N/A

0DataRank · unranked

12 citations

Sean Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Sean J. Jurgens +57 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

Assessment of aortic valve function in over 47,000 people using deep learning

European Heart Journal(2023)10.1093/eurheartj/ehad655.1708

N/A

0DataRank · unranked

0 citations

Joel Rämö, Can Hou, Sean J. Jurgens, Victor Nauffal, Jonathan W. Cunningham +9 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

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

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

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

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

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

Proteomic Profile of the ICAM1 p.K56M HFpEF Risk Variant

JACC Basic to Translational Science(2024)10.1016/j.jacbts.2024.05.016

N/A

0DataRank · unranked

4 citations

Mallory Filipp, Michael J. Zhang, Ethan D. Moser, Edward B. Thorp, Prarthana Dalal +17 more

Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis

UNC Libraries(2024)10.17615/c1sy-3719

N/A

0DataRank · unranked

0 citations

Brandon K. Fornwalt, Chrissy Austin-Tse, Mark Chaffin, B.E. Cade, J Lee +43 more

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

Nature Genetics(2025)10.1038/s41588-025-02087-4

N/A

0DataRank · unranked

55 citations

Sean L. Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Dominique M West +95 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

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

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

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

Coagulation factor XII haploinsufficiency is protective against venous thromboembolism in a population-scale multidimensional analysis

Nature Communications(2025)10.1038/s41467-025-62789-5

N/A

0DataRank · unranked

9 citations

David S. Paul, Sean J. Jurgens, Harish Eswaran, Lu-Chen Weng, Justine Ryu +16 more

Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk

Nature Genetics(2025)10.1038/s41588-025-02397-7

N/A

0DataRank · unranked

3 citations

Joel Rämö, Cody R. Hou, Sean J. Jurgens, Shaan Khurshid, Victor Nauffal +12 more

New Threshold for Defining Mild Aortic Stenosis Derived From Velocity-Encoded MRI in 60,000 Individuals

Journal of the American College of Cardiology(2025)10.1016/j.jacc.2025.01.035

N/A

0DataRank · unranked

5 citations

Joel Rämö, David Playford, Geoff Strange, Cody R. Hou, Sean J. Jurgens +13 more

Cardiac adaptation to endurance exercise training requires suppression of GDF15 via PGC-1α

Nature Cardiovascular Research(2025)10.1038/s44161-025-00712-3

N/A

0DataRank · unranked

5 citations

Haobo Li, Tevis Vitale, James Rhee, Saketh Challa, Claire Castro +31 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 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

Multi-trait polygenic risk scores improve genomic prediction of atrial fibrillation across diverse ancestries

Research Square(2025)10.21203/rs.3.rs-7713077/v1

N/A

0DataRank · unranked

0 citations

Daria Kramarenko, Marre Corver, Nobuyuki Enzan, Dominic S. Zimmerman, Patrick T. Ellinor +3 more