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:
Karen Oliver, Ingrid E. Scheffer, Mark F. Bennett, et al.
Epilepsia (2023) Vol. 64, Iss. 5, pp. 1368-1375
Open Access | Times Cited: 68
Showing 1-25 of 68 citing articles:
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: 88
Remi Stevelink, Ciarán Campbell, Siwei Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1471-1482
Open Access | Times Cited: 88
Empowering biomedical discovery with AI agents
Shanghua Gao, Ada Fang, Yepeng Huang, et al.
Cell (2024) Vol. 187, Iss. 22, pp. 6125-6151
Open Access | Times Cited: 21
Shanghua Gao, Ada Fang, Yepeng Huang, et al.
Cell (2024) Vol. 187, Iss. 22, pp. 6125-6151
Open Access | Times Cited: 21
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: 20
Ingrid E. Scheffer, Sameer M. Zuberi, Heather C. Mefford, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 20
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
Alissa M. D’Gama, Sarah Mulhern, Beth Rosen Sheidley, et al.
The Lancet Neurology (2023) Vol. 22, Iss. 9, pp. 812-825
Open Access | Times Cited: 41
Alissa M. D’Gama, Sarah Mulhern, Beth Rosen Sheidley, et al.
The Lancet Neurology (2023) Vol. 22, Iss. 9, pp. 812-825
Open Access | Times Cited: 41
Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiology
Clare L. van Eyk, Michael Fahey, Jozef Gécz
Nature Reviews Neurology (2023) Vol. 19, Iss. 9, pp. 542-555
Closed Access | Times Cited: 28
Clare L. van Eyk, Michael Fahey, Jozef Gécz
Nature Reviews Neurology (2023) Vol. 19, Iss. 9, pp. 542-555
Closed Access | Times Cited: 28
Epilepsy-associated genes: an update
Mengwen Zhang, Xiaoyu Liang, Jie Wang, et al.
Seizure (2023) Vol. 116, pp. 4-13
Closed Access | Times Cited: 26
Mengwen Zhang, Xiaoyu Liang, Jie Wang, et al.
Seizure (2023) Vol. 116, pp. 4-13
Closed Access | Times Cited: 26
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 10, pp. 1864-1879
Closed Access | Times Cited: 8
Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 10, pp. 1864-1879
Closed Access | Times Cited: 8
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders
Sheng Luo, Pengyu Wang, Peng Zhou, et al.
The American Journal of Human Genetics (2024) Vol. 112, Iss. 1, pp. 87-105
Closed Access | Times Cited: 8
Sheng Luo, Pengyu Wang, Peng Zhou, et al.
The American Journal of Human Genetics (2024) Vol. 112, Iss. 1, pp. 87-105
Closed Access | Times Cited: 8
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries
Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 18
Siwei Chen, Benjamin M. Neale, Samuel F. Berkovic
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 18
Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement
Christy W. LaFlamme, Cassandra Rastin, Soham Sengupta, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Christy W. LaFlamme, Cassandra Rastin, Soham Sengupta, et al.
Nature Communications (2024) Vol. 15, Iss. 1
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
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
Sigma-1 receptor and seizures
Edijs Vavers, Liga Zvejniece, Maija Dambrova
Pharmacological Research (2023) Vol. 191, pp. 106771-106771
Open Access | Times Cited: 14
Edijs Vavers, Liga Zvejniece, Maija Dambrova
Pharmacological Research (2023) Vol. 191, pp. 106771-106771
Open Access | Times Cited: 14
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
Karen Oliver, Marina Trivisano, Simone Mandelstam, et al.
Epilepsia (2023) Vol. 64, Iss. 5, pp. 1351-1367
Open Access | Times Cited: 13
The impact of microbiota and ketogenic diet interventions in the management of drug‐resistant epilepsy
Laura Diaz‐Marugan, Andrina Rutsch, Angela M. Kaindl, et al.
Acta Physiologica (2024) Vol. 240, Iss. 3
Open Access | Times Cited: 5
Laura Diaz‐Marugan, Andrina Rutsch, Angela M. Kaindl, et al.
Acta Physiologica (2024) Vol. 240, Iss. 3
Open Access | Times Cited: 5
Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision Medicine
Hannah R. Snyder, Puneet Jain, Rajesh RamachandranNair, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 266-266
Open Access | Times Cited: 5
Hannah R. Snyder, Puneet Jain, Rajesh RamachandranNair, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 266-266
Open Access | Times Cited: 5
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events
Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Movement Disorders in Patients With Genetic Developmental and Epileptic Encephalopathies
Sterre van der Veen, Gabrielle T. W. Tse, Alessandro Ferretti, et al.
Neurology (2023) Vol. 101, Iss. 19
Open Access | Times Cited: 11
Sterre van der Veen, Gabrielle T. W. Tse, Alessandro Ferretti, et al.
Neurology (2023) Vol. 101, Iss. 19
Open Access | Times Cited: 11
Integrative analysis of epilepsy-associated genes reveals expression-phenotype correlations
Wanhao Chi, Evangelos Kiskinis
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Wanhao Chi, Evangelos Kiskinis
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Infantile epileptic spasms syndrome: an etiologic study of 361 patients with infantile epileptic spasms syndrome
Linghui Zhu, Yuan Xia, Hao Ding, et al.
Frontiers in Pediatrics (2025) Vol. 12
Open Access
Linghui Zhu, Yuan Xia, Hao Ding, et al.
Frontiers in Pediatrics (2025) Vol. 12
Open Access
Berberine ameliorates seizure activity and cardiac dysfunction in pentylenetetrazol-kindling seizures in rats: Modulation of sigma1 receptor, Akt/eNOS signaling, and ferroptosis
Shrouk M Basiouny, Hala F. Zaki, Shimaa M. Elshazly, et al.
Neuropharmacology (2025), pp. 110295-110295
Closed Access
Shrouk M Basiouny, Hala F. Zaki, Shimaa M. Elshazly, et al.
Neuropharmacology (2025), pp. 110295-110295
Closed Access
Fulfilling the needs of caregivers in delivering health services to children with developmental and epileptic encephalopathies
Lauren Kelada, Stephanie Best, Kristine Pierce, et al.
European Journal of Paediatric Neurology (2025) Vol. 54, pp. 147-158
Open Access
Lauren Kelada, Stephanie Best, Kristine Pierce, et al.
European Journal of Paediatric Neurology (2025) Vol. 54, pp. 147-158
Open Access
Advances in genetic developmental and epileptic encephalopathies with movement disorders
Meng Yuan, Xiaoqian Wang, Zuozhen Yang, et al.
Acta Epileptologica (2025) Vol. 7, Iss. 1
Open Access
Meng Yuan, Xiaoqian Wang, Zuozhen Yang, et al.
Acta Epileptologica (2025) Vol. 7, Iss. 1
Open Access
Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic Features
Genevieve Rayner, Eliza Honybun, Melanie Bahlo, et al.
Annals of Neurology (2025)
Open Access
Genevieve Rayner, Eliza Honybun, Melanie Bahlo, et al.
Annals of Neurology (2025)
Open Access
Is Precision Therapy in Infantile-Onset Epileptic Encephalopathies Still Too Far to Call Upon?
Raffaele Falsaperla, Vincenzo Sortino, Piero Pavone
Applied Sciences (2025) Vol. 15, Iss. 5, pp. 2372-2372
Open Access
Raffaele Falsaperla, Vincenzo Sortino, Piero Pavone
Applied Sciences (2025) Vol. 15, Iss. 5, pp. 2372-2372
Open Access
