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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:

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

Showing 1-25 of 37 citing articles:

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
Thalamocortical circuits in generalized epilepsy: Pathophysiologic mechanisms and therapeutic targets
Britta E. Lindquist, Clare Timbie, Yuliya Voskobiynyk, et al.
Neurobiology of Disease (2023) Vol. 181, pp. 106094-106094
Open Access | Times Cited: 22
Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model
Yukun Yuan, Luis F. Lopez‐Santiago, Nicholas Denomme, et al.
Brain (2023) Vol. 147, Iss. 4, pp. 1231-1246
Closed Access | Times Cited: 18
Atypical absence seizures and gene variants: A gene-based review of etiology, electro-clinical features, and associated epilepsy syndrome
Xiaoyu Zhao, Zimeng He, Yumei Li, et al.
Epilepsy & Behavior (2024) Vol. 151, pp. 109636-109636
Closed Access | Times Cited: 4
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
In silico screening to search for selective sodium channel blockers: When size matters
Maximiliano José Fallico, Lucas N. Alberca, Nicolás Enrique, et al.
Brain Research (2025), pp. 149571-149571
Closed Access
Comparative assessment of artificial intelligence chatbots' performance in responding to healthcare professionals' and caregivers' questions about Dravet syndrome
Joana Jesus‐Ribeiro, Eugenia Roza, Bárbara Oliveiros, et al.
Epilepsia Open (2025)
Open Access
Autism Spectrum Disorder and Epilepsy: Pathogenetic Mechanisms and Therapeutic Implications
Alessandra Giliberti, Adele Maria Frisina, Stefania Giustiniano, et al.
Journal of Clinical Medicine (2025) Vol. 14, Iss. 7, pp. 2431-2431
Open Access
The Impact and Adherence of Ketogenic Dietary Therapies for Dravet syndrome: A systematic review and meta-analysis
Yan Li, Sisi Dai, Qingqing Deng, et al.
Seizure (2025) Vol. 130, pp. 16-24
Closed Access
Cannabidiol metabolism in vitro : the role of antiseizure medications and CYP2C19 genotypes
Nattapon Jaisupa, Michael Ashton, Sofia Birgersson
Xenobiotica (2025), pp. 1-14
Open Access
Etiological analysis of 167 cases of drug-resistant epilepsy in children
Ran-Ran Zuo, Hongfang Jin, Suzhen Sun
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2024) Vol. 50, Iss. 1
Open Access | Times Cited: 3
A tool for Dravet syndrome-associated neuropsychiatric comorbidities evaluation (DANCE)
Simona Giorgi, Stéphane Auvin, An‐Sofie Schoonjans, et al.
Epilepsy & Behavior (2024) Vol. 158, pp. 109958-109958
Open Access | Times Cited: 3
Identification of five novel SCN1A variants
Baitao Zeng, Haoyi Zhang, Qing Lu, et al.
Frontiers in Behavioral Neuroscience (2023) Vol. 17
Open Access | Times Cited: 7
Developing AAV-delivered nonsense suppressor tRNAs for neurological disorders
Jiaming Wang, Guangping Gao, Dan Wang
Neurotherapeutics (2024) Vol. 21, Iss. 4, pp. e00391-e00391
Open Access | Times Cited: 2
Neurologic orphan diseases: Emerging innovations and role for genetic treatments
Ivelina Kioutchoukova, Devon Foster, Rajvi Thakkar, et al.
World Journal of Experimental Medicine (2023) Vol. 13, Iss. 4, pp. 59-74
Open Access | Times Cited: 6
Optimizing ketogenic diet therapy for childhood epilepsy: Identifying key factors for seizure control and psychomotor enhancement
Xin Tong, Qian Wang, Jie Yang, et al.
Epilepsia (2024) Vol. 65, Iss. 10, pp. 2959-2972
Closed Access | Times Cited: 2
Preferential expression of SCN1A in GABAergic neurons improves survival and epileptic phenotype in a mouse model of Dravet syndrome
Ana Ricobaraza, María Buñuales, Manuela González-Aparicio, et al.
Journal of Molecular Medicine (2023) Vol. 101, Iss. 12, pp. 1587-1601
Open Access | Times Cited: 5
Genome-wide sequencing in children with epilepsy and developmental disorders
Е. Д. Белоусова, О. С. Грознова, V. Yu. Voinova
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2024) Vol. 69, Iss. 2, pp. 56-64
Open Access | Times Cited: 1
Interneuron FGF13 regulates seizure susceptibility via a sodium channel-independent mechanism
Susan Lin, Aravind R. Gade, Hong-Gang Wang, et al.
(2024)
Open Access | Times Cited: 1
(E)-1-(Benzo[d][1,3]dioxol-5-yl)-5,6,6-trimethylhept-4-en-3-one
Mario Rico-Molina, Joaquı́n Altarejos, Sofı́a Salido
Molbank (2024) Vol. 2024, Iss. 4, pp. M1938-M1938
Open Access | Times Cited: 1
Depressed glutamate transporter 1 expression in a mouse model of Dravet syndrome
Mustafa Q. Hameed, Benjamin Hui, Rui Lin, et al.
Annals of Clinical and Translational Neurology (2023) Vol. 10, Iss. 9, pp. 1695-1699
Open Access | Times Cited: 3
Epileptogenic focal lesions in Dravet syndrome: a warning to investigators
Rita Ventura, Álvaro Beltrán‐Corbellini, Rafael Toledano, et al.
Epileptic Disorders (2023) Vol. 26, Iss. 2, pp. 173-180
Closed Access | Times Cited: 3
Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications
Jens Schuster, Xi Lu, Yonglong Dang, et al.
(2023)
Open Access | Times Cited: 2
Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications
Jens Schuster, Xi Lu, Yonglong Dang, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 2
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
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