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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:

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

Showing 17 citing articles:

Catecholaminergic Polymorphic Ventricular Tachycardia and Early Onset Atrial Fibrillation in a Tactical Athlete with a Heterozygous Truncating Variant in TRDN
Aashish Katapadi, Thomas M. Roston, Andrew D. Krahn, et al.
HeartRhythm Case Reports (2025)
Open Access | Times Cited: 1
Advances in genetic diagnosis and therapy of hereditary heart disease: a bibliometric review from 2004 to 2024
Hernández Ma, Yun Wang, Yang Jia, et al.
Frontiers in Medicine (2025) Vol. 11
Open Access
Genetic architecture of long QT syndrome and genotype-specific treatment
Iskenderov Bg, E. A. Molokova, I. N. Mozhzhukhina
Medical alphabet (2025), Iss. 4, pp. 7-14
Closed Access
Application of next generation sequencing in cardiology: current and future precision medicine implications
Eirini Papadopoulou, Dimitra Bouzarelou, George S. Tsaousis, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 8
Dissecting the associations of KCNH2 genetic polymorphisms with various types of cardiac arrhythmias
Sen Li, Zhang Zhang, Yining Ding, et al.
Gene (2024) Vol. 899, pp. 148132-148132
Closed Access | Times Cited: 2
Fetal Arrhythmia Leading to a Diagnosis of Congenital Long QT Syndrome Type II
Aidan Milner, Lindsey Mitrani, Lauren Ferrara, et al.
JACC Case Reports (2024) Vol. 29, Iss. 4, pp. 102218-102218
Open Access | Times Cited: 1
Genetic causality between type 1 diabetes and arrhythmia identified by a two-sample Mendelian randomization study
Yudi Liu, Jin Rao, Wei Hu, et al.
Diabetes Research and Clinical Practice (2024) Vol. 213, pp. 111725-111725
Closed Access | Times Cited: 1
Pathogenesis and Clinical Characteristics of Hereditary Arrhythmia Diseases
Shuang Guo, Lingfeng Zha
Genes (2024) Vol. 15, Iss. 11, pp. 1368-1368
Open Access | Times Cited: 1
Postmortem genetic analysis of 17 sudden cardiac deaths identified nonsense and frameshift variants in two cases of arrhythmogenic cardiomyopathy
Yōichirō Takahashi, Haruki Fukuda, Akira Hayakawa, et al.
International Journal of Legal Medicine (2023) Vol. 137, Iss. 6, pp. 1927-1937
Closed Access | Times Cited: 3
Genetics in the diagnosis and treatment of cardiovascular diseases
Kevin P. Bliden, Sahib Singh, Roni Shanoada, et al.
Journal of Translational Genetics and Genomics (2024) Vol. 8, Iss. 2, pp. 186-206
Open Access
Identifying barriers to genetic testing in subspecialty cardiac care
Sierra Pond, Genevie Echols, Martin Tristani‐Firouzi, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Cardiac channelopathies in pediatrics: a genetic update
Estefanía Martinez-Barrios, Óscar Campuzano, Andrea Greco, et al.
European Journal of Pediatrics (2024) Vol. 183, Iss. 11, pp. 4635-4640
Closed Access
Causal association between common rheumatic diseases and arrhythmia: a Mendelian randomization study
Yuchen Zhang, Ling Tang, Ke Zhang, et al.
Frontiers in Cardiovascular Medicine (2024) Vol. 11
Open Access
Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic Diagnostics
Maria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, et al.
Biomolecules (2024) Vol. 14, Iss. 11, pp. 1450-1450
Open Access
Current state of genetic testing for cardiac diseases in Croatia in comparison to ESC countries: an EHRA physician-based survey results
Ivan Zeljković, Anaïs Gauthey, Martin Manninger, et al.
Cardiologia Croatica (2024) Vol. 19, Iss. 11-12, pp. 531-531
Open Access
Heartbeat: pre-eclampsia is a cardiovascular disease risk factor
Catherine M Otto
Heart (2023) Vol. 109, Iss. 6, pp. 417-419
Closed Access
Genetic causality between type 1 diabetes and arrhythmia: a two-sample Mendelian randomization study
Yudi Liu, Jin Rao, Wei Hu, et al.
Research Square (Research Square) (2023)
Open Access
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