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:

Monogenic Epilepsies
Renzo Guerrini, Simona Balestrini, Elaine Wirrell, et al.
Neurology (2021) Vol. 97, Iss. 17, pp. 817-831
Open Access | Times Cited: 61

Showing 1-25 of 61 citing articles:

Drug resistance in epilepsy
Emilio Perucca, Piero Perucca, H. Steve White, et al.
The Lancet Neurology (2023) Vol. 22, Iss. 8, pp. 723-734
Closed Access | Times Cited: 107

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

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: 89

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

MDN1 variants cause susceptibility to epilepsy
Q. G. Wen, Dongming Zhang, Yan Ding, et al.
Acta Epileptologica (2025) Vol. 7, Iss. 1
Open Access | Times Cited: 1

Drosophila melanogaster as a versatile model organism to study genetic epilepsies: An overview
Florian P. Fischer, Robin A. Karge, Yvonne G. Weber, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 21

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

Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group
Michelangelo Mancuso, Maria Papadopoulou, Yi Shiau Ng, et al.
European Journal of Neurology (2024) Vol. 31, Iss. 7
Open Access | Times Cited: 8

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery
Karen Oliver, Colin A. Ellis, Ingrid E. Scheffer, et al.
EBioMedicine (2022) Vol. 81, pp. 104079-104079
Open Access | Times Cited: 22

WWOXdevelopmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk
Karen Oliver, Marina Trivisano, Simone Mandelstam, et al.
Epilepsia (2023) Vol. 64, Iss. 5, pp. 1351-1367
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

Steps to Improve Precision Medicine in Epilepsy
Simona Balestrini, Davide Mei, Sanjay M. Sisodiya, et al.
Molecular Diagnosis & Therapy (2023) Vol. 27, Iss. 6, pp. 661-672
Open Access | Times Cited: 12

Next-generation sequencing testing in children with epilepsy reveals novel clinical, diagnostic and therapeutic implications
Magdalena Krygier, Marta Pietruszka, Marta Zawadzka, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 4

Molecular mechanism analyses of post‐traumatic epilepsy and hereditary epilepsy based on 10× single‐cell transcriptome sequencing technology
Fang Wen, Zhigang Tan, Dezhi Huang, et al.
CNS Neuroscience & Therapeutics (2024) Vol. 30, Iss. 4
Open Access | Times Cited: 4

Dysregulation of miR-146a: a causative factor in epilepsy pathogenesis, diagnosis, and prognosis
Shiqi Mao, Jinhan Wu, Jingkai Yan, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 10

Hypotheses of pathophysiological mechanisms in epileptic encephalopathies: A review
Katsuhiro Kobayashi, Takashi Shibata, Hiroki Tsuchiya, et al.
Brain and Development (2025) Vol. 47, Iss. 1, pp. 104318-104318
Open Access

High-Affinity Blocker of Insect Potassium Channels from the Venom of the Scorpion Orthochirus scrobiculosus
А. А. Волков, Andrei M. Gigolaev, Valentina A. Iunusova, et al.
Journal of Evolutionary Biochemistry and Physiology (2025) Vol. 61, Iss. 1, pp. 177-186
Closed Access

Genetics of epilepsies and current possibilities of their genetic diagnostics
Natália Forgáčová, Ingrid Lojová, Ján Radvánszky, et al.
Neurologie pro praxi (2025) Vol. 26, Iss. 1, pp. 9-16
Closed Access

Genetic aetiologies in relation to response to the ketogenic diet in 226 children with epilepsy
Maria Dahlin, Tommy Stödberg, Elisabet Ekman, et al.
Brain Communications (2025) Vol. 7, Iss. 2
Open Access

Current and Emerging Precision Therapies for Developmental and Epileptic Encephalopathies
Debopam Samanta, Sonal Bhatia, Senyene E. Hunter, et al.
Pediatric Neurology (2025) Vol. 168, pp. 67-81
Closed Access

Monogenic Epilepsies in Adult Epilepsy Clinics and Gene-Driven Approaches to Treatment
Lisa M. Clayton, Angeliki Vakrinou, Simona Balestrini, et al.
Current Neurology and Neuroscience Reports (2025) Vol. 25, Iss. 1
Open Access

Immune Modulatory Effects of Ketogenic Diet in Different Disease Conditions
Shivani Srivastava, Vishakha Anand Pawar, Anuradha Tyagi, et al.
Immuno (2022) Vol. 3, Iss. 1, pp. 1-15
Open Access | Times Cited: 16

Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implications
Purvi Majethia, Namanpreet Kaur, Selinda Mascarenhas, et al.
Clinical Genetics (2024) Vol. 105, Iss. 6, pp. 639-654
Open Access | Times Cited: 3

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