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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:

Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation
Alexander Guldmann Clausen, Oliver Bundgaard Vad, Julie Husted Andersen, et al.
Frontiers in Cardiovascular Medicine (2021) Vol. 8
Open Access | Times Cited: 24

Showing 24 citing articles:

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
Atrial fibrillation: pathophysiology, genetic and epigenetic mechanisms
Manlio Vinciguerra, Dobromir Dobrev, Stanley Nattel
The Lancet Regional Health - Europe (2024) Vol. 37, pp. 100785-100785
Open Access | Times Cited: 19
Unsupervised ensemble-based phenotyping enhances discoverability of genes related to left-ventricular morphology
Rodrigo Bonazzola, Enzo Ferrante, Nishant Ravikumar, et al.
Nature Machine Intelligence (2024) Vol. 6, Iss. 3, pp. 291-306
Open Access | Times Cited: 10
Pathophysiology and clinical relevance of atrial myopathy
Michiel Tubeeckx, Gilles W. De Keulenaer, Hein Heidbüchel, et al.
Basic Research in Cardiology (2024) Vol. 119, Iss. 2, pp. 215-242
Closed Access | Times Cited: 8
Atrial cardiomyopathy: from cell to bedside
Mengmeng Li, Yuye Ning, Gary Tse, et al.
ESC Heart Failure (2022) Vol. 9, Iss. 6, pp. 3768-3784
Open Access | Times Cited: 28
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Carolina Roselli, Ida Surakka, Morten S. Olesen, et al.
Nature Genetics (2025) Vol. 57, Iss. 3, pp. 539-547
Closed Access
Genetic and non-genetic risk factors associated with atrial fibrillation
Lindsay J. Young, Steve Antwi-Boasiako, Joel Ferrall, et al.
Life Sciences (2022) Vol. 299, pp. 120529-120529
Open Access | Times Cited: 20
Pathophysiology, molecular mechanisms, and genetics of atrial fibrillation
Han Pan, Xinxin Zhao, Xuexun Li, et al.
Human Cell (2024) Vol. 38, Iss. 1
Closed Access | Times Cited: 3
Study on Potential Differentially Expressed Genes in Idiopathic Pulmonary Fibrosis by Bioinformatics and Next-Generation Sequencing Data Analysis
Muttanagouda Giriyappagoudar, Basavaraj Vastrad, Rajeshwari Horakeri, et al.
Biomedicines (2023) Vol. 11, Iss. 12, pp. 3109-3109
Open Access | Times Cited: 7
Direct Binding of Synaptopodin 2-Like Protein to Alpha-Actinin Contributes to Actin Bundle Formation in Cardiomyocytes
Hiroshi Yamada, Hirona Osaka, Nanami Tatsumi, et al.
(2024)
Open Access | Times Cited: 1
Whole Exome Sequencing in Two Southeast Asian Families With Atypical Femur Fractures
Wei Zhou, Hanh H. Nguyen, Denise M van de Laarschot, et al.
JBMR Plus (2022) Vol. 6, Iss. 8
Open Access | Times Cited: 6
Discovery of TBX20 As a Novel Gene Underlying Atrial Fibrillation
Ning Li, Yanjie Li, Xiaojuan Guo, et al.
(2023)
Open Access | Times Cited: 3
Genetics of atrial fibrillation—an update of recent findings
Aarthi Manoharan, Sambandam Ravikumar, Vishnu Bhat Ballambattu
Molecular Biology Reports (2022) Vol. 49, Iss. 8, pp. 8121-8129
Closed Access | Times Cited: 5
Discovery of TBX20 as a Novel Gene Underlying Atrial Fibrillation
Ning Li, Yanjie Li, Xiaojuan Guo, et al.
Biology (2023) Vol. 12, Iss. 9, pp. 1186-1186
Open Access | Times Cited: 2
Study on potential differentially expressed genes in idiopathic pulmonary fibrosis by bioinformatics and next generation sequencing data analysis
Basavaraj Vastrad, Chanabasayya Vastrad
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Direct Binding of Synaptopodin 2-Like Protein to Alpha-Actinin Contributes to Actin Bundle Formation in Cardiomyocytes
Hiroshi Yamada, Hirona Osaka, Nanami Tatsumi, et al.
Cells (2024) Vol. 13, Iss. 16, pp. 1373-1373
Open Access
Pathogenetics of Cardiomyopathy
А. Н. Кучер, Aleksei A. Sleptcov, М. С. Назаренко
Russian Journal of Genetics (2023) Vol. 59, Iss. 6, pp. 527-543
Closed Access | Times Cited: 1
Ultrastructural Assessment and Proteomic Analysis in Myofibrillogenesis in the Heart Primordium After Heartbeat Initiation in Rats
Nobutoshi Ichise, Tatsuya Sato, Hiroyori Fusagawa, et al.
Frontiers in Physiology (2022) Vol. 13
Open Access | Times Cited: 1
Pathogenetics of Cardiomyopathy
А. Н. Кучер, Aleksei A. Sleptcov, М. С. Назаренко
Генетика (2023) Vol. 59, Iss. 6, pp. 615-632
Closed Access
Risk stratification of atrial fibrillation and stroke using single nucleotide polymorphism and circulating biomarkers
Tetsuo Sasano, Kensuke Ihara, Toshihiro Tanaka, et al.
PLoS ONE (2023) Vol. 18, Iss. 10, pp. e0292118-e0292118
Open Access
Cap analysis of gene expression reveals alternative promoter usage in a rat model of hypertension
Sonal Dahale, Jorge Ruiz‐Orera, Jan Šilhavý, et al.
Life Science Alliance (2022) Vol. 5, Iss. 4, pp. e202101234-e202101234
Open Access
Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes
Julian Libiseller-Egger, Jody Phelan, Zachi I. Attia, et al.
Research Square (Research Square) (2022)
Open Access
Genome-wide analyses identify SCN5A as a susceptibility locus for premature atrial contraction frequency
Sébastien Thériault, Medea Imboden, Mary L. Biggs, et al.
iScience (2022) Vol. 25, Iss. 10, pp. 105210-105210
Open Access
Cap analysis of gene expression (CAGE) sequencing reveals alternative promoter usage in complex disease
Sonal Dahale, Jorge Ruiz‐Orera, Jan Šilhavý, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
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