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:

Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies
Julia Oyrer, Snezana Maljevic, Ingrid E. Scheffer, et al.
Pharmacological Reviews (2017) Vol. 70, Iss. 1, pp. 142-173
Open Access | Times Cited: 268

Showing 26-50 of 268 citing articles:

Spectrum of GABAA receptor variants in epilepsy
Snezana Maljevic, Rikke S. Møller, Christopher A. Reid, et al.
Current Opinion in Neurology (2019) Vol. 32, Iss. 2, pp. 183-190
Closed Access | Times Cited: 75

Losing the Beat: Contribution of Purkinje Cell Firing Dysfunction to Disease, and Its Reversal
Anna A. Cook, Eviatar Fields, Alanna J. Watt
Neuroscience (2020) Vol. 462, pp. 247-261
Open Access | Times Cited: 63

Immunity, Ion Channels and Epilepsy
Tsang‐Shan Chen, Ming‐Chi Lai, Huai-Ying Ingrid Huang, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 12, pp. 6446-6446
Open Access | Times Cited: 32

Molecular mechanisms of topiramate and its clinical value in epilepsy
Yun-Fei Bai, Chang Zeng, Miaomiao Jia, et al.
Seizure (2022) Vol. 98, pp. 51-56
Open Access | Times Cited: 31

Parvalbumin Role in Epilepsy and Psychiatric Comorbidities: From Mechanism to Intervention
Lívea Dornela Godoy, Tamiris Prizon, Matheus Teixeira Rossignoli, et al.
Frontiers in Integrative Neuroscience (2022) Vol. 16
Open Access | Times Cited: 29

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

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

The effect of Ferroptosis -related Mitochondrial Dysfunction in the Development of Temporal Lobe Epilepsy
Yang Su, Ningrui Cao, Dingkun Zhang, et al.
Ageing Research Reviews (2024) Vol. 96, pp. 102248-102248
Closed Access | Times Cited: 8

Unveiling the role of histone deacetylases in neurological diseases: focus on epilepsy
Danfeng Cao, Xinyu Zhou, Qian Guo, et al.
Biomarker Research (2024) Vol. 12, Iss. 1
Open Access | Times Cited: 7

Resolving the Micro-Macro Disconnect to Address Core Features of Seizure Networks
Jordan S. Farrell, Quynh-Anh Nguyen, Iván Soltész
Neuron (2019) Vol. 101, Iss. 6, pp. 1016-1028
Open Access | Times Cited: 52

KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect
Kyle Metz, Xinchen Teng, Isabelle Coppens, et al.
Annals of Neurology (2018) Vol. 84, Iss. 5, pp. 766-780
Open Access | Times Cited: 49

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability
Mattia Bonzanni, Jacopo C. DiFrancesco, Raffaella Milanesi, et al.
Neurobiology of Disease (2018) Vol. 118, pp. 55-63
Open Access | Times Cited: 47

Technologies to Study Action Potential Propagation With a Focus on HD-MEAs
Vishalini Emmenegger, Marie Engelene J. Obien, Felix Franke, et al.
Frontiers in Cellular Neuroscience (2019) Vol. 13
Open Access | Times Cited: 46

GABAAR isoform and subunit structural motifs determine synaptic and extrasynaptic receptor localisation
Saad Hannan, Marielle Minère, Joseph Harris, et al.
Neuropharmacology (2019) Vol. 169, pp. 107540-107540
Open Access | Times Cited: 43

Enlightening the neuroprotective effect of quercetin in epilepsy: From mechanism to therapeutic opportunities
Enes Akyüz, Yam Nath Paudel, Ayse Kristina Polat, et al.
Epilepsy & Behavior (2021) Vol. 115, pp. 107701-107701
Closed Access | Times Cited: 39

Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathy
Lauren E. Bleakley, Chaseley E. McKenzie, Ming S. Soh, et al.
Brain (2021) Vol. 144, Iss. 7, pp. 2060-2073
Open Access | Times Cited: 38

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: 34

Pharmacological activation of ATF6 remodels the proteostasis network to rescue pathogenic GABAA receptors
Meng Wang, Edmund Cotter, Yajuan Wang, et al.
Cell & Bioscience (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 25

Classification of missense variants in the N-methyl-d-aspartate receptor GRIN gene family as gain- or loss-of-function
Scott J. Myers, Hongjie Yuan, Riley E. Perszyk, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 19, pp. 2857-2871
Open Access | Times Cited: 16

A Role for KCNQ Channels on Cell Type-Specific Plasticity in Mouse Auditory Cortex after Peripheral Damage
Amanda Henton, Yanjun Zhao, Thanos Tzounopoulos
Journal of Neuroscience (2023) Vol. 43, Iss. 13, pp. 2277-2290
Open Access | Times Cited: 13

Complexity in Genetic Epilepsies: A Comprehensive Review
Cassandra Rastin, Laila C. Schenkel, Bekim Sadiković
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 19, pp. 14606-14606
Open Access | Times Cited: 13

Pathogenesis, diagnosis, and treatment of epilepsy: electromagnetic stimulation–mediated neuromodulation therapy and new technologies
Dian Jiao, Lai Xu, Zhen Gu, et al.
Neural Regeneration Research (2024) Vol. 20, Iss. 4, pp. 917-935
Open Access | Times Cited: 5

The ClinGen Epilepsy Gene Curation Expert Panel—Bridging the divide between clinical domain knowledge and formal gene curation criteria
Ingo Helbig, Erin Rooney Riggs, Carrie‐Anne Barry, et al.
Human Mutation (2018) Vol. 39, Iss. 11, pp. 1476-1484
Open Access | Times Cited: 40

SCN 2A channelopathies: Mechanisms and models
Ulrike B. S. Hedrich, Stephan Lauxmann, Holger Lerche
Epilepsia (2019) Vol. 60, Iss. S3
Open Access | Times Cited: 38

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