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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:

Brugada syndrome trafficking–defective Nav1.5 channels can trap cardiac Kir2.1/2.2 channels
Marta Pérez-Hernández, Marcos Matamoros, Silvia Alfayate, et al.
JCI Insight (2018) Vol. 3, Iss. 18
Open Access | Times Cited: 46

Showing 1-25 of 46 citing articles:

Brugada Syndrome
Andrew D. Krahn, Elijah R. Behr, Robert M. Hamilton, et al.
JACC. Clinical electrophysiology (2022) Vol. 8, Iss. 3, pp. 386-405
Open Access | Times Cited: 74
Ion channel traffic jams: the significance of trafficking deficiency in long QT syndrome
Gema Mondéjar‐Parreño, Ana I. Moreno-Manuel, Juan Manuel Ruiz Robles, et al.
Cell Discovery (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 1
Cardiac potassium inward rectifier Kir2: Review of structure, regulation, pharmacology, and arrhythmogenesis
Louise Reilly, Lee L. Eckhardt
Heart Rhythm (2021) Vol. 18, Iss. 8, pp. 1423-1434
Open Access | Times Cited: 55
Maturation of hiPSC-derived cardiomyocytes promotes adult alternative splicing of SCN5A and reveals changes in sodium current associated with cardiac arrhythmia
Giulia Campostrini, Georgios Kosmidis, Dorien Ward‐van Oostwaard, et al.
Cardiovascular Research (2022) Vol. 119, Iss. 1, pp. 167-182
Open Access | Times Cited: 25
The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3
Ana I. Moreno-Manuel, Álvaro Macías, Francisco M. Cruz, et al.
Cardiovascular Research (2024) Vol. 120, Iss. 5, pp. 490-505
Open Access | Times Cited: 6
Kir2.1-NaV1.5 channelosome and its role in arrhythmias in inheritable cardiac diseases
Lilian K. Gutiérrez, Ana I. Moreno-Manuel, José Jalife
Heart Rhythm (2024) Vol. 21, Iss. 5, pp. 630-646
Closed Access | Times Cited: 5
Cardiomyocyte Microtubules: Control of Mechanics, Transport, and Remodeling
Keita Uchida, Emily A. Scarborough, Benjamin L. Prosser
Annual Review of Physiology (2021) Vol. 84, Iss. 1, pp. 257-283
Open Access | Times Cited: 31
SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients
Eric N. Jiménez‐Vázquez, Michael Arad, Álvaro Macías, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 21
Extracellular Kir2.1 C122Y Mutant Upsets Kir2.1-PIP 2 Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome
Francisco M. Cruz, Álvaro Macías, Ana I. Moreno-Manuel, et al.
Circulation Research (2024) Vol. 134, Iss. 8
Closed Access | Times Cited: 4
The network of cardiac KIR2.1: its function, cellular regulation, electrical signaling, diseases and new drug avenues
Encan Li, Marcel A. G. van der Heyden
Naunyn-Schmiedeberg s Archives of Pharmacology (2024) Vol. 397, Iss. 9, pp. 6369-6389
Open Access | Times Cited: 4
Tbx5 variants disrupt Nav1.5 function differently in patients diagnosed with Brugada or Long QT Syndrome
Paloma Nieto-Marín, David Tinaquero, Raquel G. Utrilla, et al.
Cardiovascular Research (2021) Vol. 118, Iss. 4, pp. 1046-1060
Closed Access | Times Cited: 27
Subcellular diversity of Nav1.5 in cardiomyocytes: distinct functions, mechanisms and targets
Gerard A. Marchal, Carol Ann Remme
The Journal of Physiology (2022) Vol. 601, Iss. 5, pp. 941-960
Open Access | Times Cited: 18
Two concurrent mechanisms are responsible for the INa increase produced by dapagliflozin and empagliflozin in healthy and heart failure cardiomyocytes
Josu Rapún, Sara Pérez‐Martín, Anabel Cámara‐Checa, et al.
Biomedicine & Pharmacotherapy (2025) Vol. 186, pp. 117984-117984
Closed Access
Propionic Acidemia‐Induced Proarrhythmic Electrophysiological Alterations in Human iPSC‐Derived Cardiomyocytes
Anabel Cámara‐Checa, Mar Álvarez, Josu Rapún, et al.
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 3
Open Access
Distributed synthesis of sarcolemmal and sarcoplasmic reticulum membrane proteins in cardiac myocytes
Vladimir Bogdanov, Andrew M. Soltisz, Nicolae Moise, et al.
Basic Research in Cardiology (2021) Vol. 116, Iss. 1
Open Access | Times Cited: 22
Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome
Ana I. Moreno-Manuel, Lilian K. Gutiérrez, María Linarejos Vera-Pedrosa, et al.
Cardiovascular Research (2022) Vol. 119, Iss. 4, pp. 919-932
Open Access | Times Cited: 15
N-Glycosylation of the voltage-gated sodium channel β2 subunit is required for efficient trafficking of NaV1.5/β2 to the plasma membrane
Èric Cortada, Ramón Brugada, Marcel Vergés
Journal of Biological Chemistry (2019) Vol. 294, Iss. 44, pp. 16123-16140
Open Access | Times Cited: 23
Genomic and Non-Genomic Regulatory Mechanisms of the Cardiac Sodium Channel in Cardiac Arrhythmias
Houria Daimi, Estefanía Lozano-Velasco, Amelia Aránega, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 3, pp. 1381-1381
Open Access | Times Cited: 13
Empagliflozin and Dapagliflozin Increase Na+ and Inward Rectifier K+ Current Densities in Human Cardiomyocytes Derived from Induced Pluripotent Stem Cells (hiPSC-CMs)
María Dago, Teresa Crespo‐García, Anabel Cámara‐Checa, et al.
Cells (2022) Vol. 11, Iss. 23, pp. 3707-3707
Open Access | Times Cited: 13
Long QT syndrome – Bench to bedside
Daniela Ponce‐Balbuena, Isabelle Deschênes
Heart Rhythm O2 (2021) Vol. 2, Iss. 1, pp. 89-106
Open Access | Times Cited: 16
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
Ventricular voltage‐gated ion channels: Detection, characteristics, mechanisms, and drug safety evaluation
Lulan Chen, Yue He, Xiangdong Wang, et al.
Clinical and Translational Medicine (2021) Vol. 11, Iss. 10
Open Access | Times Cited: 13
Kir2.1 dysfunction at the sarcolemma and the sarcoplasmic reticulum causes arrhythmias in a mouse model of Andersen–Tawil syndrome type 1
Álvaro Macías, Andrés González-Guerra, Ana I. Moreno-Manuel, et al.
Nature Cardiovascular Research (2022) Vol. 1, Iss. 10, pp. 900-917
Open Access | Times Cited: 10
Trafficking and Function of the Voltage-Gated Sodium Channel β2 Subunit
Èric Cortada, Ramón Brugada, Marcel Vergés
Biomolecules (2019) Vol. 9, Iss. 10, pp. 604-604
Open Access | Times Cited: 15
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
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