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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:

SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis
Jiangwei Ding, Xinxiao Li, Haiyan Tian, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 74

Showing 1-25 of 74 citing articles:

Incomplete Penetrance and Variable Expressivity: From Clinical Studies to Population Cohorts
Rebecca Kingdom, Caroline F. Wright
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 145
Interneuron FGF13 regulates seizure susceptibility via a sodium channel-independent mechanism
Susan Lin, Aravind R. Gade, Hong‐Gang Wang, et al.
eLife (2025) Vol. 13
Open Access | Times Cited: 2
Excitatory/inhibitory balance in epilepsies and neurodevelopmental disorders: Depolarizing γ‐aminobutyric acid as a common mechanism
Eline van Hugte, Dirk Schubert, Nael Nadif Kasri
Epilepsia (2023) Vol. 64, Iss. 8, pp. 1975-1990
Open Access | Times Cited: 36
Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights
Andy Cheuk‐Him Ng, Mohamed Chahine, Morris H. Scantlebury, et al.
Journal of Neurology (2024) Vol. 271, Iss. 6, pp. 3063-3094
Closed Access | Times Cited: 9
Clinical Efficacy and Safety of the Ketogenic Diet in Patients with Genetic Confirmation of Drug-Resistant Epilepsy
Jihoon Na, Hyun Joo Lee, Young‐Mock Lee
Nutrients (2025) Vol. 17, Iss. 6, pp. 979-979
Open Access | Times Cited: 1
Dravet syndrome: Advances in etiology, clinical presentation, and treatment
Zimeng He, Yumei Li, Xiaoyu Zhao, et al.
Epilepsy Research (2022) Vol. 188, pp. 107041-107041
Closed Access | Times Cited: 37
Microglia specific deletion of miR-155 in Alzheimer’s disease mouse models reduces amyloid-β pathology but causes hyperexcitability and seizures
Macarena S. Aloi, Katherine E. Prater, Raymond E.A. Sanchez, et al.
Journal of Neuroinflammation (2023) Vol. 20, Iss. 1
Open Access | Times Cited: 22
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study
Benedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1248-1248
Open Access | Times Cited: 8
Consensus panel recommendations for the optimization of EPIDIOLEX® treatment for seizures associated with Lennox–Gastaut syndrome, Dravet syndrome, and tuberous sclerosis complex
Robert T. Wechsler, David E. Burdette, Barry E. Gidal, et al.
Epilepsia Open (2024) Vol. 9, Iss. 5, pp. 1632-1642
Open Access | Times Cited: 7
NaV1.1 is essential for proprioceptive signaling and motor behaviors
Cyrrus M. Espino, Cheyanne M. Lewis, Serena Ortiz, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 26
Translation velocity determines the efficacy of engineered suppressor tRNAs on pathogenic nonsense mutations
Nikhil Bharti, Leonardo Santos, Marcos Davyt, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
SCN1A channelopathies: Navigating from genotype to neural circuit dysfunction
Alexander Bryson, Steven Petrou
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 12
Likely Pathogenic Variants of Cav1.3 and Nav1.1 Encoding Genes in Amyotrophic Lateral Sclerosis Could Elucidate the Dysregulated Pain Pathways
Zsófia Flóra Nagy, Balázs Sonkodi, Margit Pál, et al.
Biomedicines (2023) Vol. 11, Iss. 3, pp. 933-933
Open Access | Times Cited: 11
Clinical trials for Lennox–Gastaut syndrome: Challenges and priorities
Juliet K. Knowles, Aaron E. L. Warren, Ismail Mohamed, et al.
Annals of Clinical and Translational Neurology (2024) Vol. 11, Iss. 11, pp. 2818-2835
Open Access | Times Cited: 4
Mechanisms of infantile epileptic spasms syndrome: What have we learned from animal models?
Andy Cheuk‐Him Ng, Anamika Choudhary, Karlene T. Barrett, et al.
Epilepsia (2023) Vol. 65, Iss. 2, pp. 266-280
Open Access | Times Cited: 10
Abnormalities in the functional activity of neural networks in a human iPSC model of Dravet syndrome
Ropafadzo Mzezewa, Tanja Hyvärinen, Andrey Vinogradov, et al.
Research Square (Research Square) (2025)
Open Access
Expanding the Genetic and Clinical Spectrum of SCN1A-Related Hemiplegic Migraine: Analysis of Mutations in Japanese
Daisuke Danno, Haruka Tada, Itsuki Oda, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1426-1426
Open Access
Neonatal/infantile‐onset genetic epilepsies: The utility of genetic testing for molecular etiology‐specific diagnosis concerning therapeutic implications
Muhittin Özcan, Seda Kanmaz, Erdem Şimşek, et al.
Epileptic Disorders (2025)
Closed Access
Case Report of Myoclonus‐Ataxia Syndrome in an Indian Patient Due to SCNA1 Gene Mutation
Anjali Chouksey
Movement Disorders Clinical Practice (2025)
Closed Access
Assessing the diagnostic performance of investigations in pediatric myoclonic epilepsies: A retrospective cohort study
Séverine Brulé, Blandine Dozières‐Puyravel, Hala Nasser, et al.
Epilepsia (2025)
Open Access
Utility of adenoviral vectors in animal models of human disease: Genetic diseases
Rubén Hernández-Alcoceba
Elsevier eBooks (2025), pp. 727-753
Closed Access
A review of epilepsy syndromes and epileptogenic mechanism affiliated with brain tumor related genes
Chung-Kin Chan, Kheng Seang Lim, Chet-Ying Chan, et al.
Gene (2025), pp. 149531-149531
Closed Access
Personalized genetic diagnosis of hereditary neurological diseases
Т. В. Кожанова, С. С. Жилина, T. I. Mescheryakova, et al.
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2025) Vol. 70, Iss. 2/2, pp. 74-81
Open Access
mTORopathies in Epilepsy and Neurodevelopmental Disorders: The Future of Therapeutics and the Role of Gene Editing
Marina Ottmann Boff, Fernando Antônio Costa Xavier, Fernando Mendonça Diz, et al.
Cells (2025) Vol. 14, Iss. 9, pp. 662-662
Open Access
The evolving genetic landscape of neuromuscular fetal akinesias
Göknur Haliloğlu, Gianina Ravenscroft
Journal of Neuromuscular Diseases (2025)
Closed Access
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