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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:

Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
Krishna G. Aragam, Mark Chaffin, Rebecca T. Levinson, et al.
Circulation (2019) Vol. 139, Iss. 4, pp. 489-501
Open Access | Times Cited: 139

Showing 1-25 of 139 citing articles:

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Sonia Shah, Albert Henry, Carolina Roselli, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 698
Genetic drug target validation using Mendelian randomisation
Amand F. Schmidt, Chris Finan, María Gordillo‐Marañón, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 346
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Rafik Tadros, Catherine Francis, Xiao Yun Xu, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 128-134
Open Access | Times Cited: 229
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
James P. Pirruccello, Alexander G. Bick, Minxian Wang, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 203
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: 124
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Michael G. Levin, Noah L. Tsao, Pankhuri Singhal, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 77
Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study
Shuai Yuan, Paul Carter, Maria Bruzelius, et al.
EBioMedicine (2020) Vol. 59, pp. 102956-102956
Open Access | Times Cited: 117
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
Genetic Liability to Depression and Risk of Coronary Artery Disease, Myocardial Infarction, and Other Cardiovascular Outcomes
Yunlong Lu, Zhen Wang, Marios K. Georgakis, et al.
Journal of the American Heart Association (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 75
Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure
Marios Arvanitis, Emmanouil Tampakakis, Yanxiao Zhang, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 74
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
Sophie Garnier, Magdaléna Harakaľová, Stefan Weiß, et al.
European Heart Journal (2021) Vol. 42, Iss. 20, pp. 2000-2011
Open Access | Times Cited: 71
Frequency, Penetrance, and Variable Expressivity of Dilated Cardiomyopathy–Associated Putative Pathogenic Gene Variants in UK Biobank Participants
Ravi A. Shah, Babken Asatryan, Ghaith Sharaf Dabbagh, et al.
Circulation (2022) Vol. 146, Iss. 2, pp. 110-124
Open Access | Times Cited: 61
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse
Carolina Roselli, Mengyao Yu, Victor Nauffal, et al.
European Heart Journal (2022) Vol. 43, Iss. 17, pp. 1668-1680
Open Access | Times Cited: 48
Genomic approaches to identify and investigate genes associated with atrial fibrillation and heart failure susceptibility
Kush Ketan Patel, Cynthia Venkatesan, Habiba Abdelhalim, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 27
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Rafik Tadros, Sean L. Zheng, Christopher Grace, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
Profiling of the plasma proteome across different stages of human heart failure
Anna Egerstedt, John Berntsson, Maya Landenhed Smith, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 71
Genetic Liability to Insomnia and Cardiovascular Disease Risk
Susanna C. Larsson, Hugh S. Markus
Circulation (2019) Vol. 140, Iss. 9, pp. 796-798
Open Access | Times Cited: 56
Association of alcohol consumption with morbidity and mortality in patients with cardiovascular disease: original data and meta-analysis of 48,423 men and women
Chengyi Ding, Darragh O’Neill, Steven Bell, et al.
BMC Medicine (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 54
United Kingdom Biobank (UK Biobank)
Rishi Caleyachetty, Thomas J. Littlejohns, Ben Lacey, et al.
Journal of the American College of Cardiology (2021) Vol. 78, Iss. 1, pp. 56-65
Open Access | Times Cited: 52
Genetically predicted education attainment in relation to somatic and mental health
Shuai Yuan, Ying Xiong, Madeleine Michaëlsson, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 46
Genetic architecture of heart failure with preserved versus reduced ejection fraction
Jacob Joseph, Chang Liu, Qin Hui, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 37
Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failure
Iain S. Forrest, Ghislain Rocheleau, Shantanu Bafna, et al.
European Journal of Heart Failure (2022) Vol. 24, Iss. 11, pp. 2118-2127
Open Access | Times Cited: 31
Natural Language Processing for Adjudication of Heart Failure in a Multicenter Clinical Trial
Jonathan W. Cunningham, Pulkit Singh, Christopher Reeder, et al.
JAMA Cardiology (2023) Vol. 9, Iss. 2, pp. 174-174
Open Access | Times Cited: 20
Iron Deficiency: Impact on Functional Capacity and Quality of Life in Heart Failure with Preserved Ejection Fraction
A. Alcaide-Aldeano, Alberto Garay, L Alcoberro, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 4, pp. 1199-1199
Open Access | Times Cited: 49
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
Matteo D’Antonio, Jennifer Nguyen, Timothy D. Arthur, et al.
Cell Reports (2021) Vol. 37, Iss. 7, pp. 110020-110020
Open Access | Times Cited: 36
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