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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 gain of function in early infantile encephalopathy
Géza Berecki, Alexander Bryson, Jan Terhag, et al.
Annals of Neurology (2019) Vol. 85, Iss. 4, pp. 514-525
Open Access | Times Cited: 86

Showing 1-25 of 86 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: 531
Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome
Han Zhou, Chunling Chen, Anne Christiansen, et al.
Science Translational Medicine (2020) Vol. 12, Iss. 558
Closed Access | Times Cited: 262
SCN1A‐related phenotypes: Epilepsy and beyond
Ingrid E. Scheffer, Rima Nabbout
Epilepsia (2019) Vol. 60, Iss. S3
Open Access | Times Cited: 191
Deciphering the concepts behind “Epileptic encephalopathy” and “Developmental and epileptic encephalopathy”
Ingrid E. Scheffer, Jianxiang Liao
European Journal of Paediatric Neurology (2019) Vol. 24, pp. 11-14
Closed Access | Times Cited: 145
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: 92
The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications
Andreas Brunklaus, Tobias Brünger, Tony Feng, et al.
Brain (2022) Vol. 145, Iss. 11, pp. 3816-3831
Open Access | Times Cited: 82
Gene variant effects across sodium channelopathies predict function and guide precision therapy
Andreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Brain (2022) Vol. 145, Iss. 12, pp. 4275-4286
Open Access | Times Cited: 73
Cell-Selective Adeno-Associated Virus-Mediated SCN1A Gene Regulation Therapy Rescues Mortality and Seizure Phenotypes in a Dravet Syndrome Mouse Model and Is Well Tolerated in Nonhuman Primates
Annie Tanenhaus, T. D. Stowe, Andrew L. Young, et al.
Human Gene Therapy (2022) Vol. 33, Iss. 11-12, pp. 579-597
Open Access | Times Cited: 71
Rates of Status Epilepticus and Sudden Unexplained Death in Epilepsy in People With Genetic Developmental and Epileptic Encephalopathies
Alice M. Donnan, Amy L. Schneider, Sophie Russ-Hall, et al.
Neurology (2023) Vol. 100, Iss. 16
Closed Access | Times Cited: 52
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels
Henrike Heyne, David Báez-Nieto, Sumaiya Iqbal, et al.
Science Translational Medicine (2020) Vol. 12, Iss. 556
Open Access | Times Cited: 114
Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials
Wenhui Li, Amy L. Schneider, Ingrid E. Scheffer
Epilepsia (2021) Vol. 62, Iss. 9, pp. 2205-2217
Open Access | Times Cited: 86
Sodium channelopathies of skeletal muscle and brain
Massimo Mantegazza, Sandrine Cestèle, William A. Catterall
Physiological Reviews (2021) Vol. 101, Iss. 4, pp. 1633-1689
Open Access | Times Cited: 85
Biological concepts in human sodium channel epilepsies and their relevance in clinical practice
Andreas Brunklaus, Juanjiangmeng Du, Felix Steckler, et al.
Epilepsia (2020) Vol. 61, Iss. 3, pp. 387-399
Open Access | Times Cited: 77
Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies
Nathan L. Absalom, Vivian W. Y. Liao, Katrine M. Johannesen, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 53
Development and Validation of a Prediction Model for Early Diagnosis of SCN1A -Related Epilepsies
Andreas Brunklaus, Eduardo Pérez‐Palma, Ismael Ghanty, et al.
Neurology (2022) Vol. 98, Iss. 11
Open Access | Times Cited: 47
Developmentally regulated impairment of parvalbumin interneuron synaptic transmission in an experimental model of Dravet syndrome
Keisuke Kaneko, Christopher Brian Currin, Kevin M. Goff, et al.
Cell Reports (2022) Vol. 38, Iss. 13, pp. 110580-110580
Open Access | Times Cited: 47
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: 26
Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies
Davide Mei, Valentina Cetica, Carla Marini, et al.
Epilepsia (2019) Vol. 60, Iss. S3
Open Access | Times Cited: 66
Tackling Epilepsy With High-definition Precision Medicine
Hugh Kearney, Susan Byrne, Gianpiero L. Cavalleri, et al.
JAMA Neurology (2019) Vol. 76, Iss. 9, pp. 1109-1109
Closed Access | Times Cited: 55
Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
Eva Auffenberg, Ulrike B. S. Hedrich, Raffaella Barbieri, et al.
Journal of Clinical Investigation (2021) Vol. 131, Iss. 21
Open Access | Times Cited: 43
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: 17
SCN1A variants from bench to bedside—improved clinical prediction from functional characterization
Andreas Brunklaus, Stéphanie Schorge, Alexander D. Smith, et al.
Human Mutation (2019) Vol. 41, Iss. 2, pp. 363-374
Open Access | Times Cited: 54
Recent advances in treatment of epilepsy-related sodium channelopathies
Elisa Musto, Elena Gardella, Rikke S. Møller
European Journal of Paediatric Neurology (2019) Vol. 24, pp. 123-128
Closed Access | Times Cited: 51
The Role of the Persistent Sodium Current in Epilepsy
Eric R. Wengert, Manoj K. Patel
Epiliepsy currents/Epilepsy currents (2020) Vol. 21, Iss. 1, pp. 40-47
Open Access | Times Cited: 41
Somatostatin-Positive Interneurons Contribute to Seizures inSCN8AEpileptic Encephalopathy
Eric R. Wengert, Raquel M. Miralles, Kyle C. A. Wedgwood, et al.
Journal of Neuroscience (2021) Vol. 41, Iss. 44, pp. 9257-9273
Open Access | Times Cited: 37
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