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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:

SCN5A channelopathy: arrhythmia, cardiomyopathy, epilepsy and beyond
Carol Ann Remme
Philosophical Transactions of the Royal Society B Biological Sciences (2023) Vol. 378, Iss. 1879
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Epilepsy and long-term risk of arrhythmias
Jie Wang, Peiyuan Huang, Qingwei Yu, et al.
European Heart Journal (2023) Vol. 44, Iss. 35, pp. 3374-3382
Open Access | Times Cited: 40
NaV1.5 autoantibodies in Brugada syndrome: pathogenetic implications
Adriana Tarantino, Giuseppe Ciconte, Dario Melgari, et al.
European Heart Journal (2024) Vol. 45, Iss. 40, pp. 4336-4348
Open Access | Times Cited: 7
Recent insights into channelopathies
Osama F. Harraz, Eric Delpire
Physiological Reviews (2023) Vol. 104, Iss. 1, pp. 23-31
Closed Access | Times Cited: 14
Cardiac arrhythmogenesis: roles of ion channels and their functional modification
Ming Lei, Samantha C. Salvage, Antony P. Jackson, et al.
Frontiers in Physiology (2024) Vol. 15
Open Access | Times Cited: 5
Cardiomyocyte electrophysiology and its modulation: current views and future prospects
Christopher Huang, Ming Lei
Philosophical Transactions of the Royal Society B Biological Sciences (2023) Vol. 378, Iss. 1879
Open Access | Times Cited: 11
Genotype-phenotype insights of pediatric dilated cardiomyopathy
Ying Dai, Yan Wang, Youfei Fan, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access
Ventricular ion channels and arrhythmias: an overview of physiology, pathophysiology and pharmacology
Shiqi Liu, Wei Wang, Yang Yang, et al.
Medical Review (2025)
Closed Access
Age-related atrial fibrillation: is there a role for the gut microbiome?
Michael Li, Eduardo Castañeda, Robert M. Lust
(2025)
Closed Access
Antiarrhythmic drugs of class Ic in cardiology practice
S. G. Кanorskiy, Yu. A. Yuricheva
Vrach (2025), pp. 32-38
Closed Access
Ion channel expression in intrinsic cardiac neurons: new players in cardiac channelopathies?
Jocelyn Bescond, Jean‐François Faivre, André Jean, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2025) Vol. 1872, Iss. 6, pp. 119983-119983
Open Access
Effectiveness of resveratrol in inducing adeno-associated virus as a potential definitive therapy for SCN5A mutation in Brugada syndrome: a narrative review
Andin Zahrani Pateda, Azimah Azzahra, Kuni Zakiyyah Sumargo, et al.
The Egyptian Heart Journal (2025) Vol. 77, Iss. 1
Open Access
Heritability and causality of QRS duration and chronic heart failure risk
Zequn Zheng, Xinhan Li, Yongfei Song
ESC Heart Failure (2025)
Open Access
Structural basis of human Na v 1.5 gating mechanisms
Rupam Biswas, Ana Laura López-Serrano, Apoorva Purohit, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 20
Open Access
Comprehensive review on gene mutations contributing to dilated cardiomyopathy
Shipeng Wang, Zhiyu Zhang, Jiahuan He, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 9
Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained death
Sarah E. Buerki, Cordula Haas, Jacqueline Neubauer
Seizure (2023) Vol. 113, pp. 66-75
Open Access | Times Cited: 6
Risk Assessment and Personalized Treatment Options in Inherited Dilated Cardiomyopathies: A Narrative Review
Diana-Aurora Arnăutu, Dragoş Cozma, Ioan-Radu Lala, et al.
Biomedicines (2024) Vol. 12, Iss. 8, pp. 1643-1643
Open Access | Times Cited: 2
Causal association between epilepsy and its DNA methylation profile and atrial fibrillation
Zequn Zheng, Haohao Chen, Yanbin Chen, et al.
Heart Rhythm (2024)
Closed Access | Times Cited: 2
Structural basis of human Nav1.5 gating mechanisms
Rupam Biswas, Ana Laura López-Serrano, Hsiang-Ling Huang, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 1
Major Causes of Conflicting Interpretations of Variant Pathogenicity in Rare Disease: A Systematic Analysis
Tatyana E. Lazareva, Yury A. Barbitoff, Yulia A. Nasykhova, et al.
Journal of Personalized Medicine (2024) Vol. 14, Iss. 8, pp. 864-864
Open Access | Times Cited: 1
Cardiac Cross-Reactivity of NaV Autoantibodies in Metastatic Breast Cancer: A Possible Trigger for Sudden Cardiac Death
Carlo Pappone, Adriana Tarantino, Dario Melgari, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Screening of the Key Genes and Signaling Pathways for Schizophrenia Using Bioinformatics and Next Generation Sequencing Data Analysis
Basavaraj Vastrad, Chanabasayya Vastrad
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Development of automated patch clamp assays to overcome the burden of variants of uncertain significance in inheritable arrhythmia syndromes
G. Joanne, Jamie I. Vandenberg, Chai‐Ann Ng
Frontiers in Physiology (2023) Vol. 14
Open Access | Times Cited: 3
TRPV2 inhibitor tranilast prevents atrial fibrillation in rat models of pulmonary hypertension
Tianxin Ye, Zhuonan Song, Yunping Zhou, et al.
Cell Calcium (2023) Vol. 117, pp. 102840-102840
Closed Access | Times Cited: 3
Anxiety and dysautonomia symptoms in patients with a NaV1.7 mutation and the potential benefits of low-dose short-acting guanfacine
Rita de Cássia Collaço, Maxime Lammens, Carley Blevins, et al.
Clinical Autonomic Research (2023) Vol. 34, Iss. 1, pp. 191-201
Closed Access | Times Cited: 2
Polymorphic Variants of SCN5A Gene (rs41312433 and rs1805124) Associated with Coronary Artery Affliction in Patients with Severe Arrhythmias
Anna Vašků, Tomáš Novotný, Jindřich Špinar
Genes (2024) Vol. 15, Iss. 2, pp. 200-200
Open Access
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