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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‐related phenotypes: Epilepsy and beyond
Ingrid E. Scheffer, Rima Nabbout
Epilepsia (2019) Vol. 60, Iss. S3
Open Access | Times Cited: 195

Showing 1-25 of 195 citing articles:

ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
Sameer M. Zuberi, Elaine Wirrell, Elissa Yozawitz, et al.
Epilepsia (2022) Vol. 63, Iss. 6, pp. 1349-1397
Open Access | Times Cited: 541
Sodium channelopathies in neurodevelopmental disorders
Miriam H. Meisler, Sophie F. Hill, Wenxi Yu
Nature reviews. Neuroscience (2021) Vol. 22, Iss. 3, pp. 152-166
Open Access | Times Cited: 136
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Renzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
Physiological Reviews (2022) Vol. 103, Iss. 1, pp. 433-513
Open Access | Times Cited: 96
Developmental and epileptic encephalopathies
Ingrid E. Scheffer, Sameer M. Zuberi, Heather C. Mefford, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 21
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
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
Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe
Elena Cardenal‐Muñoz, Stéphane Auvin, Vicente Villanueva, et al.
Epilepsia Open (2021) Vol. 7, Iss. 1, pp. 11-26
Open Access | Times Cited: 65
The brain–heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention
Giorgio Costagliola, Alessandro Orsini, Mónica Coll, et al.
Annals of Clinical and Translational Neurology (2021) Vol. 8, Iss. 7, pp. 1557-1568
Open Access | Times Cited: 59
The clinical, economic, and humanistic burden of Dravet syndrome – A systematic literature review
Joseph Sullivan, Alison Deighton, Maria Candida Vila, et al.
Epilepsy & Behavior (2022) Vol. 130, pp. 108661-108661
Open Access | Times Cited: 43
Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition
Helena Martins Custodio, Lisa M. Clayton, Ravishankara Bellampalli, et al.
Brain (2023) Vol. 146, Iss. 9, pp. 3885-3897
Open Access | Times Cited: 32
Voltage-Gated Sodium Channel Dysfunctions in Neurological Disorders
Raffaella Barbieri, Mario Nizzari, Ilaria Zanardi, et al.
Life (2023) Vol. 13, Iss. 5, pp. 1191-1191
Open Access | Times Cited: 32
Selected Biomarkers of Oxidative Stress and Energy Metabolism Disorders in Neurological Diseases
Izabela Korczowska‐Łącka, Mikołaj Hurła, Natalia Banaszek, et al.
Molecular Neurobiology (2023) Vol. 60, Iss. 7, pp. 4132-4149
Open Access | Times Cited: 24
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
Deregulated ion channels contribute to RHOBTB2-associated developmental and epileptic encephalopathy
Franziska Langhammer, Anne Gregor, Niels R. Ntamati, et al.
Human Molecular Genetics (2025)
Open Access | Times Cited: 1
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
Intellectual functioning and behavior in Dravet syndrome: A systematic review
Josefine Soto Jansson, T Hallböök, Colin Reilly
Epilepsy & Behavior (2020) Vol. 108, pp. 107079-107079
Closed Access | Times Cited: 56
A systematic review of adults with Dravet syndrome
Arunan Selvarajah, Quratulain Zulfiqar Ali, Paula Marques, et al.
Seizure (2021) Vol. 87, pp. 39-45
Open Access | Times Cited: 52
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
Gain of function SCN1A disease‐causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication
Sara Matricardi, Sandrine Cestèle, Marina Trivisano, et al.
Epilepsia (2023) Vol. 64, Iss. 5, pp. 1331-1347
Open Access | Times Cited: 18
Therapeutic efficacy of voltage-gated sodium channel inhibitors in epilepsy
John Agbo, Zainab Gambo Ibrahim, Shehu Yakubu Magaji, et al.
Acta Epileptologica (2023) Vol. 5, Iss. 1
Open Access | Times Cited: 18
Natural product-derived therapies for treating drug-resistant epilepsies: From ethnopharmacology to evidence-based medicine
Soura Challal, Adrianna Skiba, Mélanie Langlois, et al.
Journal of Ethnopharmacology (2023) Vol. 317, pp. 116740-116740
Closed Access | Times Cited: 17
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
Improving epilepsy diagnosis across the lifespan: approaches and innovations
Jacob Pellinen, Emma Foster, Jo M. Wilmshurst, et al.
The Lancet Neurology (2024) Vol. 23, Iss. 5, pp. 511-521
Closed Access | Times Cited: 7
CRISPR-Cas9-Mediated Gene Therapy in Neurological Disorders
Lihong Guan, Yawei Han, Ciqing Yang, et al.
Molecular Neurobiology (2021) Vol. 59, Iss. 2, pp. 968-982
Closed Access | Times Cited: 40
The epilepsy–autism spectrum disorder phenotype in the era of molecular genetics and precision therapy
Nicola Specchio, Valentina Di Micco, Marina Trivisano, et al.
Epilepsia (2021) Vol. 63, Iss. 1, pp. 6-21
Closed Access | Times Cited: 35
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