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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Monogenic and Polygenic Contributions to Atrial Fibrillation Risk
Seung Hoan Choi, Sean J. Jurgens, Lu‐Chen Weng, et al.
Circulation Research (2019) Vol. 126, Iss. 2, pp. 200-209
Open Access | Times Cited: 99

Showing 1-25 of 99 citing articles:

2023 ACC/AHA/ACCP/HRS Guideline for the Diagnosis and Management of Atrial Fibrillation: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines
José A. Joglar, Mina K. Chung, Anastasia L. Armbruster, et al.
Circulation (2023) Vol. 149, Iss. 1
Open Access | Times Cited: 882
2023 ACC/AHA/ACCP/HRS Guideline for the Diagnosis and Management of Atrial Fibrillation
José A. Joglar, Mina K. Chung, Anastasia L. Armbruster, et al.
Journal of the American College of Cardiology (2023) Vol. 83, Iss. 1, pp. 109-279
Open Access | Times Cited: 261
Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association
Jack W. O’Sullivan, Sridharan Raghavan, Carla Márquez‐Luna, et al.
Circulation (2022) Vol. 146, Iss. 8
Open Access | Times Cited: 245
Genetics of Atrial Fibrillation in 2020
Carolina Roselli, Michiel Rienstra, Patrick T. Ellinor
Circulation Research (2020) Vol. 127, Iss. 1, pp. 21-33
Open Access | Times Cited: 157
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
Sean J. Jurgens, Seung Hoan Choi, Valerie N. Morrill, et al.
Nature Genetics (2022) Vol. 54, Iss. 3, pp. 240-250
Open Access | Times Cited: 125
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Zachary T. Yoneda, Katherine Anderson, Joseph A. Quintana, et al.
JAMA Cardiology (2021) Vol. 6, Iss. 12, pp. 1371-1371
Open Access | Times Cited: 116
Epidemiology of Atrial Fibrillation
Juqian Zhang, Søren Paaske Johnsen, Yutao Guo, et al.
Cardiac Electrophysiology Clinics (2021) Vol. 13, Iss. 1, pp. 1-23
Closed Access | Times Cited: 114
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Julien Barc, Rafik Tadros, Charlotte Glinge, et al.
Nature Genetics (2022) Vol. 54, Iss. 3, pp. 232-239
Open Access | Times Cited: 105
Management of Atrial Fibrillation Across the Spectrum of Heart Failure With Preserved and Reduced Ejection Fraction
Yogesh N.V. Reddy, Barry A. Borlaug, Bernard J. Gersh
Circulation (2022) Vol. 146, Iss. 4, pp. 339-357
Open Access | Times Cited: 78
2024 HRS expert consensus statement on arrhythmias in the athlete: Evaluation, treatment, and return to play
Rachel Lampert, Eugene H. Chung, Michael J. Ackerman, et al.
Heart Rhythm (2024) Vol. 21, Iss. 10, pp. e151-e252
Closed Access | Times Cited: 23
Computational models of atrial fibrillation: achievements, challenges, and perspectives for improving clinical care
Jordi Heijman, Henry Sutanto, Harry J.G.M. Crijns, et al.
Cardiovascular Research (2021) Vol. 117, Iss. 7, pp. 1682-1699
Open Access | Times Cited: 63
NOTCH3 variants are more common than expected in the general population and associated with stroke and vascular dementia: an analysis of 200 000 participants
Bernard P. H. Cho, Stefania Nannoni, Eric L. Harshfield, et al.
Journal of Neurology Neurosurgery & Psychiatry (2021) Vol. 92, Iss. 7, pp. 694-701
Open Access | Times Cited: 59
A polygenic risk score predicts atrial fibrillation in cardiovascular disease
Nicholas Marston, Amanda C. Garfinkel, Frederick Kamanu, et al.
European Heart Journal (2022) Vol. 44, Iss. 3, pp. 221-231
Open Access | Times Cited: 43
Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank
Kiran J. Biddinger, Sean J. Jurgens, Dimitri J. Maamari, et al.
JAMA Cardiology (2022) Vol. 7, Iss. 7, pp. 715-715
Open Access | Times Cited: 42
Association of Vascular Risk Factors and Genetic Factors With Penetrance of Variants Causing Monogenic Stroke
Bernard P. H. Cho, Eric L. Harshfield, Maha Al-Thani, et al.
JAMA Neurology (2022) Vol. 79, Iss. 12, pp. 1303-1303
Open Access | Times Cited: 40
Innovative approaches to atrial fibrillation prediction: should polygenic scores and machine learning be implemented in clinical practice?
Adrian Petzl, Gilbert Jabbour, Julia Cadrin‐Tourigny, et al.
EP Europace (2024) Vol. 26, Iss. 8
Open Access | Times Cited: 12
Current RNA strategies in treating cardiovascular diseases
Shirley Pei Shan Chia, Jeremy Kah Sheng Pang, Boon-Seng Soh
Molecular Therapy (2024) Vol. 32, Iss. 3, pp. 580-608
Open Access | Times Cited: 8
JCS/JCC/JSPCCS 2024 Guideline on Genetic Testing and Counseling in Cardiovascular Disease
Yasushi Imai, Kengo Kusano, Takeshi Aiba, et al.
Journal of Cardiology (2025) Vol. 85, Iss. 2, pp. 115-176
Open Access | Times Cited: 1
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J. Jurgens, Ling Xiao, et al.
Nature Genetics (2025)
Closed Access | Times Cited: 1
Towards precision medicine in heart failure
Chad S. Weldy, Euan A. Ashley
Nature Reviews Cardiology (2021) Vol. 18, Iss. 11, pp. 745-762
Closed Access | Times Cited: 54
Polygenic risk scores for the prediction of cardiometabolic disease
Jack W. O’Sullivan, Euan A. Ashley, Perry Elliott
European Heart Journal (2022) Vol. 44, Iss. 2, pp. 89-99
Closed Access | Times Cited: 37
Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization
Anna Lewis, Emma Perez, Anya E. R. Prince, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 34
Monogenic and Polygenic Contributions to QTc Prolongation in the Population
Victor Nauffal, Valerie N. Morrill, Sean J. Jurgens, et al.
Circulation (2022) Vol. 145, Iss. 20, pp. 1524-1533
Open Access | Times Cited: 30
Current State and Future of Polygenic Risk Scores in Cardiometabolic Disease: A Scoping Review
Jobanjit Phulka, Mishal Ashraf, Beenu K. Bajwa, et al.
Circulation Genomic and Precision Medicine (2023) Vol. 16, Iss. 3, pp. 286-313
Closed Access | Times Cited: 17
Genetic testing in early-onset atrial fibrillation
Shinwan Kany, Sean J. Jurgens, Joel Rämö, et al.
European Heart Journal (2024) Vol. 45, Iss. 34, pp. 3111-3123
Closed Access | Times Cited: 7
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