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:

Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology
Robert S. Fisher, J. Helen Cross, Jacqueline A. French, et al.
Epilepsia (2017) Vol. 58, Iss. 4, pp. 522-530
Open Access | Times Cited: 2850

Showing 51-75 of 2850 citing articles:

Association of Closed-Loop Brain Stimulation Neurophysiological Features With Seizure Control Among Patients With Focal Epilepsy
Vasileios Kokkinos, Nathaniel Sisterson, Thomas A. Wozny, et al.
JAMA Neurology (2019) Vol. 76, Iss. 7, pp. 800-800
Open Access | Times Cited: 127

GSK-3β at the Intersection of Neuronal Plasticity and Neurodegeneration
Tomasz Jaworski, Ewa Banach, Katarzyna Gralec
Neural Plasticity (2019) Vol. 2019, pp. 1-14
Open Access | Times Cited: 127

Machine learning and wearable devices of the future
Sándor Beniczky, Philippa J. Karoly, Ewan S. Nurse, et al.
Epilepsia (2020) Vol. 62, Iss. S2
Open Access | Times Cited: 124

Developmental and epileptic encephalopathies: what we do and do not know
Nicola Specchio, Paolo Curatolo
Brain (2020) Vol. 144, Iss. 1, pp. 32-43
Open Access | Times Cited: 124

A taxonomy of seizure dynamotypes
Maria Luisa Saggio, Dakota Crisp, Jared M. Scott, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 123

Neurologic phenotypes associated with COL4A1 / 2 mutations
Sara Zagaglia, C. Selch, Jelena Radić Nišević, et al.
Neurology (2018) Vol. 91, Iss. 22
Open Access | Times Cited: 122

Genetic epilepsy with febrile seizures plus
Yuehua Zhang, Rosemary Burgess, Jodie P. Malone, et al.
Neurology (2017) Vol. 89, Iss. 12, pp. 1210-1219
Closed Access | Times Cited: 121

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias
Katherine L. Helbig, Robert J. Lauerer, Jacqueline C Bahr, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 5, pp. 666-678
Open Access | Times Cited: 121

Classification of the epilepsies: New concepts for discussion and debate—Special report of the ILAE Classification Task Force of the Commission for Classification and Terminology
Ingrid E. Scheffer, Jacqueline A. French, Édouard Hirsch, et al.
Epilepsia Open (2016) Vol. 1, Iss. 1-2, pp. 37-44
Open Access | Times Cited: 119

Defining the phenotypic spectrum of SLC6A1 mutations
Katrine M. Johannesen, Elena Gardella, Tarja Linnankivi, et al.
Epilepsia (2018) Vol. 59, Iss. 2, pp. 389-402
Open Access | Times Cited: 119

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy
Melodie R. Winawer, Nicole G. Griffin, Jorge Samanamud, et al.
Annals of Neurology (2018) Vol. 83, Iss. 6, pp. 1133-1146
Open Access | Times Cited: 116

Seizure outcomes in patients with anti‐NMDARencephalitis: A follow‐up study
Xu Liu, Bo Yan, Rui Wang, et al.
Epilepsia (2017) Vol. 58, Iss. 12, pp. 2104-2111
Open Access | Times Cited: 113

From Genetic Testing to Precision Medicine in Epilepsy
Pasquale Striano, Berge A. Minassian
Neurotherapeutics (2020) Vol. 17, Iss. 2, pp. 609-615
Open Access | Times Cited: 113

Standardized computer-based organized reporting of EEG: SCORE – Second version
Sándor Beniczky, Harald Aurlien, Jan Brøgger, et al.
Clinical Neurophysiology (2017) Vol. 128, Iss. 11, pp. 2334-2346
Open Access | Times Cited: 111

A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy
Ingo Helbig, Tania López-Hernández, Oded Shor, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1060-1072
Open Access | Times Cited: 108

Epilepsy genetics: Current knowledge, applications, and future directions
Kenneth A. Myers, Devon L. Johnstone, David A. Dyment
Clinical Genetics (2018) Vol. 95, Iss. 1, pp. 95-111
Open Access | Times Cited: 106

Neuropharmacology of Antiseizure Drugs
Tahir Hakami
Neuropsychopharmacology Reports (2021) Vol. 41, Iss. 3, pp. 336-351
Open Access | Times Cited: 103

Epilepsy Overview and Revised Classification of Seizures and Epilepsies
Alison Pack
CONTINUUM Lifelong Learning in Neurology (2019) Vol. 25, Iss. 2, pp. 306-321
Closed Access | Times Cited: 101

Perampanel in routine clinical use in idiopathic generalized epilepsy: The 12-month GENERAL study
Vicente Villanueva, Javier Montoya, Ascensión Castillo, et al.
Epilepsia (2018) Vol. 59, Iss. 9, pp. 1740-1752
Open Access | Times Cited: 100

The expanded clinical spectrum of anti-GABABR encephalitis and added value of KCTD16 autoantibodies
Marleen H. van Coevorden‐Hameete, Marienke A.A.M. de Bruijn, Esther de Graaff, et al.
Brain (2019) Vol. 142, Iss. 6, pp. 1631-1643
Open Access | Times Cited: 97

Epilepsy: A Clinical Overview
Tracey Milligan
The American Journal of Medicine (2021) Vol. 134, Iss. 7, pp. 840-847
Closed Access | Times Cited: 97

The postictal state — What do we know?
Julia Pottkämper, Jeannette Hofmeijer, Jeroen A. van Waarde, et al.
Epilepsia (2020) Vol. 61, Iss. 6, pp. 1045-1061
Open Access | Times Cited: 93

Epileptic seizures
Haleema Anwar, Qudsia Umaira Khan, Natasha Nadeem, et al.
Discoveries (2020) Vol. 8, Iss. 2, pp. e110-e110
Open Access | Times Cited: 93

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