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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.

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Showing 1-25 of 36 citing articles:

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Remi Stevelink, Ciarán Campbell, Siwei Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1471-1482
Open Access | Times Cited: 91
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries
Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 18
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 10, pp. 1864-1879
Closed Access | Times Cited: 8
Identification of Arrhythmia-Associated Gene Mutations in Chinese Patients with Primary Electrical Disorders or Sudden Cardiac Death
Yuxing Liu, Yi-Qiao Hu, Siyuan Zhang, et al.
Cardiovascular Innovations and Applications (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 6
RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia
Meigang Ma, Xiao‐Rong Liu, Yuan Wu, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 30
GRIN2A Variants Associated With Idiopathic Generalized Epilepsies
Xiao‐Rong Liu, Xingxing Xu, Si‐Mei Lin, et al.
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 28
Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene
Vikas Bansal, Bernhard R. Winkelmann, Johannes W. Dietrich, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 4
50 Years of Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) – Time to Explore the Dark Side of the Moon
Andreas Pflaumer, Arthur A.M. Wilde, Fatmeh Charafeddine, et al.
Heart Lung and Circulation (2019) Vol. 29, Iss. 4, pp. 520-528
Closed Access | Times Cited: 32
Genetics, manifestations, and management of catecholaminergic polymorphic ventricular tachycardia
Shubh Desai, Oliver M. Moore, Xander H.T. Wehrens
Current Opinion in Cardiology (2025)
Closed Access
“Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?
Yvonne Sleiman, Alain Lacampagne, Albano C. Méli
Cell Death and Disease (2021) Vol. 12, Iss. 11
Open Access | Times Cited: 18
Gene mutations in comorbidity of epilepsy and arrhythmia
Cheng Yu, Xuejun Deng, Da Xu
Journal of Neurology (2022) Vol. 270, Iss. 3, pp. 1229-1248
Closed Access | Times Cited: 12
Intracellular calcium homeostasis and its dysregulation underlying epileptic seizures
Xu Zhou, Zengqiang Chen, Xiao Lin, et al.
Seizure (2022) Vol. 103, pp. 126-136
Open Access | Times Cited: 12
Epilepsy and Cardiac Arrhythmias
Francis J. Ha, Timothy Chong, Mark Cook, et al.
JACC. Clinical electrophysiology (2024)
Closed Access | Times Cited: 2
Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: A Translational Perspective for the Clinician-Scientist
Dania Kallas, Avani Lamba, Thomas M. Roston, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 17, pp. 9293-9293
Open Access | Times Cited: 16
Genome-wide meta-analysis of over 29,000 people with epilepsy reveals 26 loci and subtype-specific genetic architecture
Samuel F. Berkovic, Gianpiero L. Cavalleri, Bobby P.C. Koeleman
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 11
A novel RyR2 mutation associated with co-morbid catecholaminergic polymorphic ventricular tachycardia (CPVT) and benign epilepsy with centrotemporal spikes (BECTS)
Yinxue Xing, Cui Tao, Fan Sun
Journal of Electrocardiology (2024) Vol. 84, pp. 75-80
Closed Access | Times Cited: 2
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia
Xiao‐Rong Liu, Ting‐Ting Ye, Wenjun Zhang, et al.
CNS Neuroscience & Therapeutics (2021) Vol. 27, Iss. 10, pp. 1146-1156
Open Access | Times Cited: 14
TRPM7 kinase mediates hypomagnesemia-induced seizure-related death
Man Liu, Hong Liu, Feng Feng, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 5
Genetic Testing in Epilepsy
David M. Ritter, Katherine Holland
Seminars in Neurology (2020) Vol. 40, Iss. 06, pp. 730-738
Closed Access | Times Cited: 11
Biallelic ADGRV1 variants are associated with Rolandic epilepsy
Zhigang Liu, Xingguang Ye, Jieyan Zhang, et al.
Neurological Sciences (2021) Vol. 43, Iss. 2, pp. 1365-1374
Closed Access | Times Cited: 10
Genetic generalized epilepsy with catecholaminergic polymorphic ventricular tachycardia complicated by ryanodine receptor 2 variant: A case report
Kazutoshi Konomatsu, Yosuke Kakisaka, Kazutaka Jin, et al.
Seizure (2024) Vol. 117, pp. 284-287
Open Access | Times Cited: 1
Treatment Outcomes in Children With Catecholaminergic Polymorphic Ventricular Tachycardia: A Single Institutional Experience
Joowon Lee, Bo Sang Kwon, Mi Kyoung Song, et al.
Korean Circulation Journal (2024) Vol. 54, Iss. 12, pp. 853-853
Closed Access | Times Cited: 1
RyR2 disease mutations at the C-terminal domain intersubunit interface alter closed-state stability and channel activation
Wenting Guo, Jinhong Wei, John Paul Estillore, et al.
Journal of Biological Chemistry (2021) Vol. 297, Iss. 1, pp. 100808-100808
Open Access | Times Cited: 9
CPVT and Complete Atrio-Ventricular Block: The Flipside of the Same Coin
Mattia Petrungaro, Antonio Scarà, Alessio Borrelli, et al.
Journal of Cardiovascular Development and Disease (2023) Vol. 10, Iss. 3, pp. 97-97
Open Access | Times Cited: 3
Neurologic complications of genetic channelopathies
Wayne H. Franklin, Matthew Laubham
Handbook of clinical neurology (2021), pp. 185-188
Closed Access | Times Cited: 7
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