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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:

Genetic insight into sick sinus syndrome
Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Hildur M. Aegisdottir, et al.
European Heart Journal (2021) Vol. 42, Iss. 20, pp. 1959-1971
Open Access | Times Cited: 45

Showing 1-25 of 45 citing articles:

Association of Sinoatrial Node Radiation Dose With Atrial Fibrillation and Mortality in Patients With Lung Cancer
Kyung Hwan Kim, Jaewon Oh, Gowoon Yang, et al.
JAMA Oncology (2022) Vol. 8, Iss. 11, pp. 1624-1624
Open Access | Times Cited: 57
The impact of common and rare genetic variants on bradyarrhythmia development
Lu‐Chen Weng, Joel Rämö, Sean J. Jurgens, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
Regulatory network and targeted interventions for CCDC family in tumor pathogenesis
Zhen Liu, Weiwei Yan, Shaohua Liu, et al.
Cancer Letters (2023) Vol. 565, pp. 216225-216225
Closed Access | Times Cited: 20
Pharmacological mechanism of natural drugs and their active ingredients in the treatment of arrhythmia via calcium channel regulation
Xinai Zhang, Yuqian Gao, Yutong Zhou, et al.
Biomedicine & Pharmacotherapy (2023) Vol. 160, pp. 114413-114413
Open Access | Times Cited: 19
Genetic insights into cardiac conduction disorders from genome-wide association studies
Bingxun Li, Hongxuan Xu, Lin Wu
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
HCN4 and Arrhythmias: Insights into Base Mutations
Wei Fan, Xuemei Sun, R Yuan, et al.
Mutation Research/Reviews in Mutation Research (2025) Vol. 795, pp. 108534-108534
Closed Access
Causality of Childhood and Adult Body Mass Index on Sick Sinus Syndrome: A Mendelian Randomization Study
Guanzhen Xu, Zhuang Liu, Ping Hou
Cureus (2025)
Open Access
Significance of α-Myosin Heavy Chain (MYH6) Variants in Hypoplastic Left Heart Syndrome and Related Cardiovascular Diseases
Melissa Anfinson, R. H. Fitts, John Lough, et al.
Journal of Cardiovascular Development and Disease (2022) Vol. 9, Iss. 5, pp. 144-144
Open Access | Times Cited: 18
Association between sick sinus syndrome and atrial fibrillation: A systematic review and meta-analysis
Ying Liu, Yi Zheng, Gary Tse, et al.
International Journal of Cardiology (2023) Vol. 381, pp. 20-36
Closed Access | Times Cited: 10
Identification and functional analysis of variants of MYH6 gene promoter in isolated ventricular septal defects
Ji-Yang Zuo, Huanxin Chen, Zhigang Liu, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 13
Predictors of pacemaker requirement in patients with implantable loop recorder and unexplained syncope: A systematic review and meta‐analysis
Moein Zangiabadian, Kiarash Soltani, Yasaman Gholinejad, et al.
Clinical Cardiology (2024) Vol. 47, Iss. 2
Open Access | Times Cited: 2
Identification of pleiotropic and specific therapeutic targets for cardio-cerebral diseases: A large-scale proteome-wide mendelian randomization and colocalization study
Yanchen Zhu, Yahui Wang, Zhaorui Cui, et al.
PLoS ONE (2024) Vol. 19, Iss. 5, pp. e0300500-e0300500
Open Access | Times Cited: 2
Genetic basis and causal relationship between atrial fibrillation and sinus node dysfunction: Evidence from comprehensive genetic analysis
Zhaoqi Yan, Xiangyi Pu, Xing Chang, et al.
International Journal of Cardiology (2024) Vol. 418, pp. 132609-132609
Closed Access | Times Cited: 2
Relevance of mitochondrial oxidative stress to arrhythmias: Innovative concepts to target treatments
Can Liu, Ning Ma, Ziru Guo, et al.
Pharmacological Research (2021) Vol. 175, pp. 106027-106027
Closed Access | Times Cited: 17
A phenotype-based forward genetic screen identifies Dnajb6 as a sick sinus syndrome gene
Yonghe Ding, Di Lang, Jianhua Yan, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 10
Regulation of cardiac ion channels by transcription factors: Looking for new opportunities of druggable targets for the treatment of arrhythmias
Teresa Crespo-García, Anabel Cámara-Checa, María Dago, et al.
Biochemical Pharmacology (2022) Vol. 204, pp. 115206-115206
Open Access | Times Cited: 9
RA signaling pathway combined with Wnt signaling pathway regulates human-induced pluripotent stem cells (hiPSCs) differentiation to sinus node-like cells
Lin Yin, Feng-Yuan Wang, Wei Zhang, et al.
Stem Cell Research & Therapy (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 8
Inherited and Acquired Rhythm Disturbances in Sick Sinus Syndrome, Brugada Syndrome, and Atrial Fibrillation: Lessons from Preclinical Modeling
Laura Iop, Sabino Iliceto, Giovanni Civieri, et al.
Cells (2021) Vol. 10, Iss. 11, pp. 3175-3175
Open Access | Times Cited: 11
Pausa Sinusal
Martha Cecilia Guiracocha-Arizaga, Susana Janeth Peña Cordero, Marcia Yolanda Cobos-Alvarracín
MQRInvestigar (2024) Vol. 8, Iss. 1, pp. 1963-1975
Open Access | Times Cited: 1
Improved Strategies for Modeling Sick Sinus Syndrome in Rats: Balancing Efficacy and Animal Care
Liming He, Xinxin Shi, Yucheng Wang, et al.
(2024)
Open Access | Times Cited: 1
Causal inference in the field of arrhythmia: An introduction to mendelian randomization
Eva Lukas, Margot P. van de Weijer, Jacob Bergstedt, et al.
Heart Rhythm (2024)
Closed Access | Times Cited: 1
Zfhx3 Transcription Factor Represses the Expression of SCN5A Gene and Decreases Sodium Current Density (INa)
Marcos Rubio-Alarcón, Anabel Cámara-Checa, María Dago, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 23, pp. 13031-13031
Open Access | Times Cited: 10
Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases
Ina Holst Laursen, Karina Banasik, Amalie Dahl Haue, et al.
BMJ Open (2021) Vol. 11, Iss. 12, pp. e049709-e049709
Open Access | Times Cited: 8
GJA1 gene polymorphism is a genetic predictor of recurrence after pulmonary vein isolation in patients with paroxysmal atrial fibrillation
Sho Okamura, Hidenori Ochi, Yuko Onohara, et al.
Heart Rhythm (2022) Vol. 19, Iss. 12, pp. 2044-2050
Closed Access | Times Cited: 5
Epistasis regulates genetic control of cardiac hypertrophy
Qianru Wang, Tiffany M. Tang, Nathan Youlton, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
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