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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:

Genotype–phenotype associations in 1018 individuals with SCN1A‐related epilepsies
D.S. Gallagher, Eduardo Pérez‐Palma, Tobias Bruenger, et al.
Epilepsia (2024) Vol. 65, Iss. 4, pp. 1046-1059
Open Access | Times Cited: 16

Showing 16 citing articles:

The epilepsy–autism phenotype associated with developmental and epileptic encephalopathies: New mechanism‐based therapeutic options
Nicola Specchio, Valentina Di Micco, Eleonora Aronica, et al.
Epilepsia (2025)
Closed Access | Times Cited: 1
Long-Term Seizure Reduction Associated with Vagal Nerve Stimulation in Dravet Syndrome
Sunanjay Bajaj, Alina Ivaniuk, Tobias Bruenger, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Analysis of initial seizure characteristics in patients with infantile onset genetic epilepsy
Youngkyu Shim, Hunmin Kim, Jong‐Hee Chae, et al.
Brain and Development (2025) Vol. 47, Iss. 1, pp. 104319-104319
Closed Access
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B. Howell, Susan M. White, Amy McTague, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access
History, mystery, and prospects in SCN1A channelopathies/channelepsies
Shyi-Jou Chen
Pediatrics & Neonatology (2025)
Open Access
Delphi consensus on referral criteria for pediatric patients with suspected Dravet syndrome
Ángel Aledo‐Serrano, Susana Boronat, Juan José Garcı́a-Peñas, et al.
Epilepsy & Behavior (2025) Vol. 167, pp. 110401-110401
Closed Access
Comprehensive Genetic Diagnosis and Therapeutic Perspectives in 155 Children with Developmental and Epileptic Encephalopathy.
Roxane Van Heurck, Eva Hammar, Dorothée Ville, et al.
European Journal of Paediatric Neurology (2025) Vol. 56, pp. 97-103
Closed Access
From All to One: Can a Large Cohort of Individuals with SCN1A-Related Epilepsy Offer Predictions for Other Individuals With SCN1A Variants?
Elizabeth E. Gerard
Epiliepsy currents/Epilepsy currents (2025)
Open Access
Familial SYNGAP1 variants define the boundaries of a complex neurodevelopmental disorder with epilepsy
Abiola Harrison, Jan Magielski, Ian McSalley, et al.
Epilepsia (2025)
Open Access
SCN1A—Characterization of the Gene’s Variants in the Polish Cohort of Patients with Dravet Syndrome: One Center Experience
Elżbieta Stawicka, A Zielińska, Paulina Górka-Skoczylas, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 5, pp. 4437-4451
Open Access | Times Cited: 1
Fine mapping and candidate gene analysis of Dravet syndrome modifier loci on mouse chromosomes 7 and 8
Nicole A. Hawkins, Nathan Speakes, Jennifer A. Kearney
Mammalian Genome (2024) Vol. 35, Iss. 3, pp. 334-345
Open Access | Times Cited: 1
The epilepsy phenotype of KCNK4-related neurodevelopmental disease
Magdalena Krygier, Szymon Ziętkiewicz, Weronika Talaśka-Liczbik, et al.
Seizure (2024) Vol. 121, pp. 114-122
Closed Access | Times Cited: 1
Quantitative EEG Spectral Features Differentiate Genetic Epilepsies and Predict Neurologic Outcomes
Peter D. Galer, Jillian L. McKee, Sarah M. Ruggiero, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
The cytokine receptor Fn14 is a molecular brake on neuronal activity that mediates circadian function in vivo
Austin Ferro, Anosha Arshad, L. Adlai Boyd, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Fine Mapping and Candidate Gene Analysis of Dravet Syndrome Modifier Loci on Mouse Chromosomes 7 and 8
Nicole A. Hawkins, Nathan Speakes, Jennifer A. Kearney
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
How Has the Treatment of Polish Children with Dravet Syndrome Changed? Future Perspectives
A Zielińska, Urszula Skarżyńska, Paulina Górka-Skoczylas, et al.
Biomedicines (2024) Vol. 12, Iss. 6, pp. 1249-1249
Open Access
Research progress on pathogenesis and treatment of febrile seizures
Chang L. Wu, Qingmei Wang, Wei Li, et al.
Life Sciences (2024), pp. 123360-123360
Closed Access
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