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:
Variable Expression of GABAA Receptor Subunit Gamma 2 Mutation in a Nuclear Family Displaying Developmental and Encephalopathic Phenotype
Gerald Nwosu, Shilpa B. Reddy, Heather Riordan, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 17, pp. 9683-9683
Open Access | Times Cited: 8
Gerald Nwosu, Shilpa B. Reddy, Heather Riordan, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 17, pp. 9683-9683
Open Access | Times Cited: 8
Showing 8 citing articles:
Navigating Uncertainty: Assessing Variants of Uncertain Significance in the CDKL5 Gene for Developmental and Epileptic Encephalopathy Using In Silico Prediction Tools and Computational Analysis
Özlem Yalçın Çapan
Journal of Molecular Neuroscience (2025) Vol. 75, Iss. 1
Closed Access
Özlem Yalçın Çapan
Journal of Molecular Neuroscience (2025) Vol. 75, Iss. 1
Closed Access
Differential inflammation responses determine the variable phenotypes of epilepsy induced by GABRG2 mutations
Jiahui Sui, Longwu Zhan, Shengtao Ji, et al.
CNS Neuroscience & Therapeutics (2024) Vol. 30, Iss. 2
Open Access | Times Cited: 3
Jiahui Sui, Longwu Zhan, Shengtao Ji, et al.
CNS Neuroscience & Therapeutics (2024) Vol. 30, Iss. 2
Open Access | Times Cited: 3
The modern approaches to the diagnostics and treatment of Lennox–Gastaut syndrome (literature review)
К. Yu. Мukhin, О. А. Пылаева
Russian Journal of Child Neurology (2024) Vol. 18, Iss. 4, pp. 36-43
Open Access | Times Cited: 1
К. Yu. Мukhin, О. А. Пылаева
Russian Journal of Child Neurology (2024) Vol. 18, Iss. 4, pp. 36-43
Open Access | Times Cited: 1
GABRG2 mutations in genetic epilepsy with febrile seizures plus: structure, roles, and molecular genetics
Xinxiao Li, Shengnan Guo, Yangyang Sun, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
Xinxiao Li, Shengnan Guo, Yangyang Sun, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
GABAA Receptor β3 Subunit Mutation N328D Heterozygous Knock-in Mice Have Lennox–Gastaut Syndrome
Gerald Nwosu, Wangzhen Shen, Kirill Zavalin, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8458-8458
Open Access | Times Cited: 3
Gerald Nwosu, Wangzhen Shen, Kirill Zavalin, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8458-8458
Open Access | Times Cited: 3
GABA(A) Receptor Subunit (γ2, δ, β1-3) Variants in Genetic Epilepsy: A Comprehensive Summary of 206 Clinical Cases
Xinyi Zhu, Peijun Li
Journal of Child Neurology (2024)
Closed Access
Xinyi Zhu, Peijun Li
Journal of Child Neurology (2024)
Closed Access
Slow Down and Seize: Seizures Triggered by Slow Wave Oscillations in a GABAergic Model of Dravet Syndrome
Gordon F. Buchanan
Epiliepsy currents/Epilepsy currents (2023) Vol. 23, Iss. 4, pp. 254-256
Open Access | Times Cited: 1
Gordon F. Buchanan
Epiliepsy currents/Epilepsy currents (2023) Vol. 23, Iss. 4, pp. 254-256
Open Access | Times Cited: 1
Editorial: In vivo investigations on neurological disorders: From traditional approaches to forefront technologies
Giulia Curia, Erika Estrada‐Camarena, Elı́as Manjarrez, et al.
Frontiers in Neuroscience (2022) Vol. 16
Open Access
Giulia Curia, Erika Estrada‐Camarena, Elı́as Manjarrez, et al.
Frontiers in Neuroscience (2022) Vol. 16
Open Access
