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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:

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
Katrine M. Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Brain (2021) Vol. 145, Iss. 9, pp. 2991-3009
Open Access | Times Cited: 110

Showing 1-25 of 110 citing articles:

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
Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progress
Juliet K. Knowles, Ingo Helbig, Cameron S. Metcalf, et al.
Epilepsia (2022) Vol. 63, Iss. 10, pp. 2461-2475
Open Access | Times Cited: 91
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Remi Stevelink, Ciarán Campbell, Siwei Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1471-1482
Open Access | Times Cited: 91
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: 86
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
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
Voltage-gated sodium channels in excitable cells as drug targets
Matthew Alsaloum, Sulayman D. Dib‐Hajj, Dana A. Page, et al.
Nature Reviews Drug Discovery (2025)
Closed Access | Times Cited: 3
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: 54
The current landscape of epilepsy genetics: where are we, and where are we going?
Sarah M. Ruggiero, Julie Xian, Ingo Helbig
Current Opinion in Neurology (2023)
Open Access | Times Cited: 28
Molecular and cellular context influences SCN8A variant function
Carlos G. Vanoye, Т. В. Абрамова, Jean‐Marc DeKeyser, et al.
JCI Insight (2024) Vol. 9, Iss. 12
Open Access | Times Cited: 11
Cenobamate as add‐on treatment for SCN8A developmental and epileptic encephalopathy
Cathrine E. Gjerulfsen, Madeleine J. Oudin, Francesca Furia, et al.
Epilepsia (2025)
Closed Access | Times Cited: 1
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
Management of Developmental and Epileptic Encephalopathies
Alejandra Vasquez, Anthony L. Fine
Seminars in Neurology (2025)
Closed Access | Times Cited: 1
Distinguishing Loss-of-Function and Gain-of-Function SCN8A Variants Using a Random Forest Classification Model Trained on Clinical Features
Joshua Hack, Kyle J. Horning, Denise M. Juroske Short, et al.
Neurology Genetics (2023) Vol. 9, Iss. 3
Open Access | Times Cited: 20
Structure of human NaV1.6 channel reveals Na+ selectivity and pore blockade by 4,9-anhydro-tetrodotoxin
Yue Li, Tian Yuan, Bo Huang, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 19
Global modified‐Delphi consensus on comorbidities and prognosis of SCN8A‐related epilepsy and/or neurodevelopmental disorders
Gabrielle Conecker, Maya Xia, JayEtta Hecker, et al.
Epilepsia (2024) Vol. 65, Iss. 8, pp. 2308-2321
Open Access | Times Cited: 8
Genetic Background of Epilepsy and Antiepileptic Treatments
Kinga K. Borowicz-Reutt, Julia Czernia, Marlena Krawczyk
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 22, pp. 16280-16280
Open Access | Times Cited: 16
Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson’s study
Sinthuja Pachchek, Zied Landoulsi, Lukas Pavelka, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 14
Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A‐related epilepsy and/or neurodevelopmental disorders
Gabrielle Conecker, Maya Xia, JayEtta Hecker, et al.
Epilepsia (2024) Vol. 65, Iss. 8, pp. 2322-2338
Open Access | Times Cited: 6
The expanding field of genetic developmental and epileptic encephalopathies: current understanding and future perspectives
Nicola Specchio, Marina Trivisano, Eleonora Aronica, et al.
The Lancet Child & Adolescent Health (2024) Vol. 8, Iss. 11, pp. 821-834
Closed Access | Times Cited: 6
Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy
Shir Quinn, Nan Zhang, Timothy A. Fenton, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 5, pp. 167127-167127
Open Access | Times Cited: 5
Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes
Tobias Brünger, Eduardo Pérez‐Palma, Ludovica Montanucci, et al.
Brain (2022) Vol. 146, Iss. 3, pp. 923-934
Open Access | Times Cited: 21
Predicting functional effects of ion channel variants using new phenotypic machine learning methods
Christian M. Boßelmann, Ulrike B. S. Hedrich, Holger Lerche, et al.
PLoS Computational Biology (2023) Vol. 19, Iss. 3, pp. e1010959-e1010959
Open Access | Times Cited: 13
Biallelic structural variations withinFGF12detected by long-read sequencing in epilepsy
Sachiko Ohori, Akihiko Miyauchi, Hitoshi Osaka, et al.
Life Science Alliance (2023) Vol. 6, Iss. 8, pp. e202302025-e202302025
Open Access | Times Cited: 13
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