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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:

Characteristics of KCNQ2 variants causing either benign neonatal epilepsy or developmental and epileptic encephalopathy
Goto Ayako, Atsushi Ishii, Mami Shibata, et al.
Epilepsia (2019) Vol. 60, Iss. 9, pp. 1870-1880
Open Access | Times Cited: 85

Showing 1-25 of 85 citing articles:

ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
Sameer M. Zuberi, Elaine Wirrell, Elissa Yozawitz, et al.
Epilepsia (2022) Vol. 63, Iss. 6, pp. 1349-1397
Open Access | Times Cited: 531
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: 123
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction
Piera Nappi, Francesco Miceli, Maria Virginia Soldovieri, et al.
Pflügers Archiv - European Journal of Physiology (2020) Vol. 472, Iss. 7, pp. 881-898
Closed Access | Times Cited: 84
Genetic potassium channel-associated epilepsies: Clinical review of the Kv family
Nicholas M. Allen, Sarah Weckhuysen, Kathleen M. Gorman, et al.
European Journal of Paediatric Neurology (2019) Vol. 24, pp. 105-116
Open Access | Times Cited: 83
Potassium channels and epilepsy
Kai Gao, Zehong Lin, Sijia Wen, et al.
Acta Neurologica Scandinavica (2022) Vol. 146, Iss. 6, pp. 699-707
Closed Access | Times Cited: 46
High-throughput evaluation of epilepsy-associated KCNQ2 variants reveals functional and pharmacological heterogeneity
Carlos G. Vanoye, Reshma R. Desai, Zhigang Ji, et al.
JCI Insight (2022) Vol. 7, Iss. 5
Open Access | Times Cited: 41
Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy
Timothy J Abreo, Emma C. Thompson, Anuraag Madabushi, et al.
eLife (2025) Vol. 13
Open Access | Times Cited: 1
Identifying mutation hotspots reveals pathogenetic mechanisms of KCNQ2 epileptic encephalopathy
Jiaren Zhang, Eung Chang Kim, Congcong Chen, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 56
Potassium channelopathies associated with epilepsy-related syndromes and directions for therapeutic intervention
Valentin K. Gribkoff, Raymond J. Winquist
Biochemical Pharmacology (2023) Vol. 208, pp. 115413-115413
Closed Access | Times Cited: 19
Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy
Dina Simkin, Kelly A. Marshall, Carlos G. Vanoye, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 36
Epilepsy and Cognitive Impairment in Childhood and Adolescence: A Mini-Review
Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, Andrea Viggiano, et al.
Current Neuropharmacology (2022) Vol. 21, Iss. 8, pp. 1646-1665
Closed Access | Times Cited: 27
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
Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes
Tobias Brünger, Eduardo Pérez‐Palma, Ludovica Montanucci, et al.
Brain (2022) Vol. 146, Iss. 3, pp. 923-934
Open Access | Times Cited: 21
Genetic features and pharmacological rescue of novel Kv7.2 variants in patients with epilepsy
Yuelin Song, Xia Yang, Ziyue Peng, et al.
Journal of Medical Genetics (2025), pp. jmg-110141
Closed Access
Biophysical and structural mechanisms of epilepsy-associated mutations in the S4-S5 Linker of KCNQ2 channels
Inn‐Chi Lee, Yen-Yu Yang, Hsueh‐Kai Chang, et al.
Channels (2025) Vol. 19, Iss. 1
Open Access
Potassium current inactivation as a novel pathomechanism for KCNQ2 developmental and epileptic encephalopathy
Ingride Luzio Gaspar, Gaetano Terrone, Giusy Carleo, et al.
Epilepsia (2025)
Open Access
A case of early epileptic encephalopathy caused by new mutation at W218C in KCNQ2 and review literature
Yang Ju-hua, Yuping Huang, Zhijun Chen, et al.
Biochemistry and Biophysics Reports (2025) Vol. 42, pp. 102008-102008
Closed Access
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants
Federica Malerba, Giulio Alberini, Ganna Balagura, et al.
Neurology Genetics (2020) Vol. 6, Iss. 6
Open Access | Times Cited: 29
Potassium channels as prominent targets and tools for the treatment of epilepsy
Е. С. Никитин, Lyudmila V. Vinogradova
Expert Opinion on Therapeutic Targets (2021), pp. 1-13
Closed Access | Times Cited: 27
Genetic variations associated with pharmacoresistant epilepsy (Review)
Noem� C�rdenas‐Rodr�guez, Liliana Carmona‐Aparicio, Diana P�rez‐Lozano, et al.
Molecular Medicine Reports (2020)
Open Access | Times Cited: 24
Adult phenotype of KCNQ2 encephalopathy
Stephanie Boets, Katrine M. Johannesen, Anne Destrėe, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 6, pp. 528-535
Open Access | Times Cited: 23
ILAE Genetic Literacy Series: Self‐limited familial epilepsy syndromes with onset in neonatal age and infancy
Charissa Millevert, Sarah Weckhuysen
Epileptic Disorders (2023) Vol. 25, Iss. 4, pp. 445-453
Open Access | Times Cited: 8
Clinical characteristics of KCNQ2 encephalopathy
Hyo Jeong Kim, Donghwa Yang, Se Hee Kim, et al.
Brain and Development (2020) Vol. 43, Iss. 2, pp. 244-250
Closed Access | Times Cited: 23
PIP2-dependent coupling of voltage sensor and pore domains in Kv7.2 channel
Shashank Pant, Jiaren Zhang, Eung Chang Kim, et al.
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 20
Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy
Laura Mary, Elsa Nourisson, Claire Feger, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 6, pp. 1803-1815
Closed Access | Times Cited: 17
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