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: Novel Approaches for the Most Common Genetic Epilepsy
Lori L. Isom, Kelly G. Knupp
Neurotherapeutics (2021) Vol. 18, Iss. 3, pp. 1524-1534
Open Access | Times Cited: 24

Showing 24 citing articles:

New Trends and Most Promising Therapeutic Strategies for Epilepsy Treatment
Antonella Riva, Alice Golda, Ganna Balagura, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 48

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

Epilepsy and Cognitive Impairment in Childhood and Adolescence: A Mini-Review
Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, Andrea Viggiano, et al.
Current Neuropharmacology (2022) Vol. 21, Iss. 8, pp. 1646-1665
Closed Access | Times Cited: 27

A registry for Dravet syndrome: The Italian experience
Simona Balestrini, Viola Doccini, Sabrina Giometto, et al.
Epilepsia Open (2023) Vol. 8, Iss. 2, pp. 517-534
Open Access | Times Cited: 14

Antisense oligonucleotides as a precision therapy for developmental and epileptic encephalopathies
Paloma García Quilón, Greta Volpedo, Serena Cappato, et al.
CNS Neuroscience & Therapeutics (2024) Vol. 30, Iss. 11
Open Access | Times Cited: 6

Spotlight on mechanism of sudden unexpected death in epilepsy in Dravet syndrome
WeiHui Shao, Lu Liu, JiaXuan Gu, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access

Ontology accelerates few-shot learning capability of large language model: A study in extraction of drug efficacy in a rare pediatric epilepsy
Pedram Golnari, Katrina Prantzalos, Veronica Hood, et al.
International Journal of Medical Informatics (2025), pp. 105942-105942
Open Access

CRISPR activation rescues abnormalities in SCN2A haploinsufficiency-associated autism spectrum disorder
Serena Tamura, Andrew D. Nelson, Perry W.E. Spratt, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 16

Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases
Chun‐Hong Chen, Fang Fang, Xu Wang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 16

Testing of putative antiseizure medications in a preclinical Dravet syndrome zebrafish model
Paige Whyte-Fagundes, Anjelica Vance, Aloe Carroll, et al.
Brain Communications (2024) Vol. 6, Iss. 3
Open Access | Times Cited: 3

Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome
Robert Lersch, Rawan Jannadi, Leonie Grosse, et al.
The Neuroscientist (2022) Vol. 29, Iss. 6, pp. 732-750
Open Access | Times Cited: 12

Intranasal Microemulsion as an Innovative and Promising Alternative to the Oral Route in Improving Stiripentol Brain Targeting
Sara Meirinho, Márcio Rodrigues, Adriana O. Santos, et al.
Pharmaceutics (2023) Vol. 15, Iss. 6, pp. 1641-1641
Open Access | Times Cited: 7

Heat-induced seizures, premature mortality, and hyperactivity in a novel Scn1a nonsense model for Dravet syndrome
Anat Mavashov, Marina Brusel, Jiaxing Liu, et al.
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 6

Genetic exploration of Dravet syndrome: two case report
Agung Triono, Elisabeth Siti Herini, Gunadi Gunadi
Journal of Medical Case Reports (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 1

Gene therapy for Dravet syndrome: promises and impact on disease trigger and secondary modifications
Claudia Di Berardino, Luca Massimino, Federica Ungaro, et al.
Rare Disease and Orphan Drugs Journal (2024) Vol. 3, Iss. 3
Open Access | Times Cited: 1

Transcranial static magnetic stimulation reduces seizures in a mouse model of Dravet syndrome
Casto Rivadulla, José L. Pardo‐Vázquez, Carmen de Labra, et al.
Experimental Neurology (2023) Vol. 370, pp. 114581-114581
Open Access | Times Cited: 2

Precision Treatments in Epilepsy
Scott Demarest, Amy R. Brooks‐Kayal
Neurotherapeutics (2021) Vol. 18, Iss. 3, pp. 1429-1431
Open Access | Times Cited: 4

Dravet Syndrome: An Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina
Roberto Caraballo, Gabriel Veneruzzo, Mariana Loos, et al.
Journal of Pediatric Epilepsy (2024) Vol. 13, Iss. 02, pp. 031-039
Closed Access

Heat-induced seizures, premature mortality, and hyperactivity in a novelScn1anonsense model for Dravet syndrome
Anat Mavashov, Marina Brusel, Jiaxing Liu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access

Tratamientos empleados para el síndrome de Dravet
María Cielo Duran Guerrero, Juan Carlos Pozo Palacios
Revista Vive (2023) Vol. 6, Iss. 16, pp. 172-182
Open Access

Testing of putative antiseizure drugs in a preclinical Dravet syndrome zebrafish model
Paige Whyte-Fagundes, Awais Z Vance, A Carroll, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access

The future of FS, FSE, and their epileptogenic and cognitive outcomes
Carl E. Stafstrom, Shlomo Shinnar, Tallie Z. Baram
Elsevier eBooks (2022), pp. 341-344
Closed Access

Antisense Molecules in Epilepsy—A Neuropharmacological Educational Review
J Stephen, Jesiha George Stephen, Mohammed K. Ali, et al.
International Journal of Epilepsy (2022) Vol. 08, Iss. 02, pp. 044-051
Open Access

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