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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:

Variant Intronic Enhancer Controls SCN10A-short Expression and Heart Conduction
Joyce C.K. Man, Fernanda M. Bosada, Koen T. Scholman, et al.
Circulation (2021) Vol. 144, Iss. 3, pp. 229-242
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

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: 20
Mechanisms of torsades de pointes: an update
Yukiomi Tsuji, Masatoshi Yamazaki, Masafumi Shimojo, et al.
Frontiers in Cardiovascular Medicine (2024) Vol. 11
Open Access | Times Cited: 8
SCN10A-short gene therapy to restore conduction and protect against malignant cardiac arrhythmias
Jianan Wang, Arie O. Verkerk, Ronald Wilders, et al.
European Heart Journal (2025)
Open Access | Times Cited: 1
Cavβ1 regulates T cell expansion and apoptosis independently of voltage-gated Ca2+ channel function
Serap Erdogmus, Axel R. Concepcion, Megumi Yamashita, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 30
Exploring noncoding variants in genetic diseases: from detection to functional insights
Ke Wu, Fengxiao Bu, Yang Wu, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2024) Vol. 51, Iss. 2, pp. 111-132
Open Access | Times Cited: 8
Gene therapy targeting INa to treat life-threatening arrhythmias: beyond proof-of-concept?
Patrick Lugenbiel
European Heart Journal (2025)
Closed Access
Characterization of novel arrhythmogenic patterns arising secondary to heterogeneous expression and activation of Nav1.8
Zhonghe Zhang, Héctor Barajas-Martínez, Hong-Yi Duan, et al.
Frontiers in Cardiovascular Medicine (2025) Vol. 12
Open Access
Sensory neuron sodium channels as pain targets; from cocaine to Journavx (VX-548, suzetrigine)
John N. Wood, Nieng Yan, Jian Huang, et al.
The Journal of General Physiology (2025) Vol. 157, Iss. 4
Closed Access
Cardiogenetics: the role of genetic testing for inherited arrhythmia syndromes and sudden death
Mark Specterman, Elijah R. Behr
Heart (2022) Vol. 109, Iss. 6, pp. 434-441
Open Access | Times Cited: 17
The Anti-Epileptic Drugs Lamotrigine and Valproic Acid Reduce the Cardiac Sodium Current
Lixia Jia, Arie O. Verkerk, Hanno L. Tan
Biomedicines (2023) Vol. 11, Iss. 2, pp. 477-477
Open Access | Times Cited: 7
Genetics of sinoatrial node function and heart rate disorders
Lieve E. van der Maarel, Alex V. Postma, Vincent M. Christoffels
Disease Models & Mechanisms (2023) Vol. 16, Iss. 5
Open Access | Times Cited: 7
Stem cell models of inherited arrhythmias
Tammy Ryan, Jason D. Roberts
Nature Cardiovascular Research (2024) Vol. 3, Iss. 4, pp. 420-430
Closed Access | Times Cited: 2
Transcriptional regulation of the postnatal cardiac conduction system heterogeneity
Yena Oh, Rimshah Abid, Saif Dababneh, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Clinical Characteristics, Genetic Findings and Arrhythmic Outcomes of Patients with Catecholaminergic Polymorphic Ventricular Tachycardia from China: A Systematic Review
Justin Leung, Sharen Lee, Jiandong Zhou, et al.
Life (2022) Vol. 12, Iss. 8, pp. 1104-1104
Open Access | Times Cited: 10
Patient-specific induced pluripotent stem cell properties implicate Ca 2+ -homeostasis in clinical arrhythmia associated with combined heterozygous RYR2 and SCN10A variants
Yafei Zhou, Wenjun Huang, Leiying Liu, et al.
Philosophical Transactions of the Royal Society B Biological Sciences (2023) Vol. 378, Iss. 1879
Open Access | Times Cited: 5
Case report: State-of-the-art risk-modifying treatment of sudden cardiac death in an asymptomatic patient with a mutation in the SCN5A gene and a review of the literature
Petar Brlek, Eduard Pavelić, Jana Mešić, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 4
Differential Regulation of Male-Hormones-Related Enhancers Revealed by Chromatin Accessibility and Transcriptional Profiles in Pig Liver
Shuheng Chan, Yubei Wang, Yabiao Luo, et al.
Biomolecules (2024) Vol. 14, Iss. 4, pp. 427-427
Open Access | Times Cited: 1
Differential Sodium Current Remodelling Identifies Distinct Cellular Proarrhythmic Mechanisms in Paroxysmal vs Persistent Atrial Fibrillation
Simona Casini, Gerard A. Marchal, Makiri Kawasaki, et al.
Canadian Journal of Cardiology (2022) Vol. 39, Iss. 3, pp. 277-288
Open Access | Times Cited: 7
Coronary Artery Disease Risk GenePRDM16is Preferentially Expressed in Vascular Smooth Muscle Cells and a Potential Novel Regulator of Smooth Muscle Homeostasis
Kunzhe Dong, Xiangqin He, Guoqing Hu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Cis-Cardio: A comprehensive analysis platform for cardiovascular-relavant cis-regulation in human and mouse
Chao Song, Yuexin Zhang, Hong Huang, et al.
Molecular Therapy — Nucleic Acids (2023) Vol. 33, pp. 655-667
Open Access | Times Cited: 3
Noncoding RNAs and Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes in Cardiac Arrhythmic Brugada Syndrome
Benjamin E. Theisen, Austin Holtz, Viswanathan Rajagopalan
Cells (2023) Vol. 12, Iss. 19, pp. 2398-2398
Open Access | Times Cited: 3
A rare non-coding enhancer variant inSCN5Acontributes to the high prevalence of Brugada syndrome in Thailand
Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population
Christian Paludan‐Müller, Simon Birksø Larsen, Gustav Ahlberg, et al.
Circulation Genomic and Precision Medicine (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Two distinct mechanisms for Nav1.7 null analgesia
Alexandros H. Kanellopoulos, Na-Xi Tian, James J. Cox, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Transcriptional Regulation of the Postnatal Cardiac Conduction System Heterogeneity
Kyoung-Han Kim, Yena Oh, Rimshah Abid, et al.
Research Square (Research Square) (2024)
Open Access
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