
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:
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: 134
Miriam H. Meisler, Sophie F. Hill, Wenxi Yu
Nature reviews. Neuroscience (2021) Vol. 22, Iss. 3, pp. 152-166
Open Access | Times Cited: 134
Showing 1-25 of 134 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: 94
Renzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
Physiological Reviews (2022) Vol. 103, Iss. 1, pp. 433-513
Open Access | Times Cited: 94
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
Andreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Brain (2022) Vol. 145, Iss. 12, pp. 4275-4286
Open Access | Times Cited: 73
Structural biology and molecular pharmacology of voltage-gated ion channels
Jian Huang, Xiaojing Pan, Nieng Yan
Nature Reviews Molecular Cell Biology (2024) Vol. 25, Iss. 11, pp. 904-925
Closed Access | Times Cited: 23
Jian Huang, Xiaojing Pan, Nieng Yan
Nature Reviews Molecular Cell Biology (2024) Vol. 25, Iss. 11, pp. 904-925
Closed Access | Times Cited: 23
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
Matthew Alsaloum, Sulayman D. Dib‐Hajj, Dana A. Page, et al.
Nature Reviews Drug Discovery (2025)
Closed Access | Times Cited: 3
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
Susan Lin, Aravind R. Gade, Hong‐Gang Wang, et al.
eLife (2025) Vol. 13
Open Access | Times Cited: 2
Assessing the landscape of STXBP1-related disorders in 534 individuals
Julie Xian, Shridhar Parthasarathy, Sarah M. Ruggiero, et al.
Brain (2021) Vol. 145, Iss. 5, pp. 1668-1683
Open Access | Times Cited: 80
Julie Xian, Shridhar Parthasarathy, Sarah M. Ruggiero, et al.
Brain (2021) Vol. 145, Iss. 5, pp. 1668-1683
Open Access | Times Cited: 80
Antisense Oligonucleotide Therapy for Neurodevelopmental Disorders
Sophie F. Hill, Miriam H. Meisler
Developmental Neuroscience (2021) Vol. 43, Iss. 3-4, pp. 247-252
Open Access | Times Cited: 69
Sophie F. Hill, Miriam H. Meisler
Developmental Neuroscience (2021) Vol. 43, Iss. 3-4, pp. 247-252
Open Access | Times Cited: 69
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: 30
Raffaella Barbieri, Mario Nizzari, Ilaria Zanardi, et al.
Life (2023) Vol. 13, Iss. 5, pp. 1191-1191
Open Access | Times Cited: 30
Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties
Christopher H. Thompson, F Potet, Tatiana V. Abramova, et al.
The Journal of General Physiology (2023) Vol. 155, Iss. 10
Open Access | Times Cited: 29
Christopher H. Thompson, F Potet, Tatiana V. Abramova, et al.
The Journal of General Physiology (2023) Vol. 155, Iss. 10
Open Access | Times Cited: 29
Ion channels in osteoarthritis: emerging roles and potential targets
Renpeng Zhou, Wenyu Fu, Dmytro V. Vasylyev, et al.
Nature Reviews Rheumatology (2024) Vol. 20, Iss. 9, pp. 545-564
Closed Access | Times Cited: 8
Renpeng Zhou, Wenyu Fu, Dmytro V. Vasylyev, et al.
Nature Reviews Rheumatology (2024) Vol. 20, Iss. 9, pp. 545-564
Closed Access | Times Cited: 8
Differential encoding of mammalian proprioception by voltage-gated sodium channels
Cyrrus M. Espino, Chetan Nagaraja, Serena Ortiz, et al.
Science Advances (2025) Vol. 11, Iss. 2
Open Access | Times Cited: 1
Cyrrus M. Espino, Chetan Nagaraja, Serena Ortiz, et al.
Science Advances (2025) Vol. 11, Iss. 2
Open Access | Times Cited: 1
SCN8A Epilepsy, Developmental Encephalopathy, and Related Disorders
Dinesh Talwar, Michael F. Hammer
Pediatric Neurology (2021) Vol. 122, pp. 76-83
Closed Access | Times Cited: 50
Dinesh Talwar, Michael F. Hammer
Pediatric Neurology (2021) Vol. 122, pp. 76-83
Closed Access | Times Cited: 50
Dendritic Integration Dysfunction in Neurodevelopmental Disorders
Andrew D. Nelson, Kevin J. Bender
Developmental Neuroscience (2021) Vol. 43, Iss. 3-4, pp. 201-221
Open Access | Times Cited: 46
Andrew D. Nelson, Kevin J. Bender
Developmental Neuroscience (2021) Vol. 43, Iss. 3-4, pp. 201-221
Open Access | Times Cited: 46
Ion Channels and Transporters as Therapeutic Agents: From Biomolecules to Supramolecular Medicinal Chemistry
Giacomo Picci, Silvia Marchesan, Claudia Caltagirone
Biomedicines (2022) Vol. 10, Iss. 4, pp. 885-885
Open Access | Times Cited: 30
Giacomo Picci, Silvia Marchesan, Claudia Caltagirone
Biomedicines (2022) Vol. 10, Iss. 4, pp. 885-885
Open Access | Times Cited: 30
Mechanisms Underlying Circuit Dysfunction in Neurodevelopmental Disorders
David Exposito-Alonso, Beatriz Rico
Annual Review of Genetics (2022) Vol. 56, Iss. 1, pp. 391-422
Closed Access | Times Cited: 28
David Exposito-Alonso, Beatriz Rico
Annual Review of Genetics (2022) Vol. 56, Iss. 1, pp. 391-422
Closed Access | Times Cited: 28
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
Joshua Hack, Kyle J. Horning, Denise M. Juroske Short, et al.
Neurology Genetics (2023) Vol. 9, Iss. 3
Open Access | Times Cited: 20
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons
Reza Asadollahi, Igor Delvendahl, Roman Muff, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 13, pp. 2192-2204
Open Access | Times Cited: 19
Reza Asadollahi, Igor Delvendahl, Roman Muff, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 13, pp. 2192-2204
Open Access | Times Cited: 19
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
Sara Matricardi, Sandrine Cestèle, Marina Trivisano, et al.
Epilepsia (2023) Vol. 64, Iss. 5, pp. 1331-1347
Open Access | Times Cited: 17
Overarching pathomechanisms in inherited peripheral neuropathies, spastic paraplegias, and cerebellar ataxias
Liedewei Van de Vondel, Jonathan De Winter, Vincent Timmerman, et al.
Trends in Neurosciences (2024) Vol. 47, Iss. 3, pp. 227-238
Closed Access | Times Cited: 6
Liedewei Van de Vondel, Jonathan De Winter, Vincent Timmerman, et al.
Trends in Neurosciences (2024) Vol. 47, Iss. 3, pp. 227-238
Closed Access | Times Cited: 6
Scn1a haploinsufficiency in the prefrontal cortex engages to cognitive impairment and depressive phenotype
Maurizio S. Riga, Mercedes Pérez-Fernández, Lluís Miquel-Rio, et al.
Brain (2024)
Open Access | Times Cited: 6
Maurizio S. Riga, Mercedes Pérez-Fernández, Lluís Miquel-Rio, et al.
Brain (2024)
Open Access | Times Cited: 6
Hyperexcitability and Pharmacological Responsiveness of Cortical Neurons Derived from Human iPSCs Carrying Epilepsy-Associated Sodium Channel Nav1.2-L1342P Genetic Variant
Zhefu Que, Maria I. Olivero-Acosta, Jingliang Zhang, et al.
Journal of Neuroscience (2021) Vol. 41, Iss. 49, pp. 10194-10208
Open Access | Times Cited: 36
Zhefu Que, Maria I. Olivero-Acosta, Jingliang Zhang, et al.
Journal of Neuroscience (2021) Vol. 41, Iss. 49, pp. 10194-10208
Open Access | Times Cited: 36
Deficiency of autism-related Scn2a gene in mice disrupts sleep patterns and circadian rhythms
Zhixiong Ma, Muriel Eaton, Yushuang Liu, et al.
Neurobiology of Disease (2022) Vol. 168, pp. 105690-105690
Open Access | Times Cited: 24
Zhixiong Ma, Muriel Eaton, Yushuang Liu, et al.
Neurobiology of Disease (2022) Vol. 168, pp. 105690-105690
Open Access | Times Cited: 24
MicroRNA-335-5p suppresses voltage-gated sodium channel expression and may be a target for seizure control
Mona Heiland, Niamh M. C. Connolly, Omar Mamad, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 30
Open Access | Times Cited: 15
Mona Heiland, Niamh M. C. Connolly, Omar Mamad, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 30
Open Access | Times Cited: 15
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: 15
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: 15
Nav1.2 and BK channel interaction shapes the action potential in the axon initial segment
Luiza Filipis, Laila Ananda Blömer, Jérôme Montnach, et al.
The Journal of Physiology (2023) Vol. 601, Iss. 10, pp. 1957-1979
Open Access | Times Cited: 14
Luiza Filipis, Laila Ananda Blömer, Jérôme Montnach, et al.
The Journal of Physiology (2023) Vol. 601, Iss. 10, pp. 1957-1979
Open Access | Times Cited: 14