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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:

Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature
Claire Bar, Giulia Barcia, Mélanie Jennesson, et al.
Human Mutation (2019) Vol. 41, Iss. 1, pp. 69-80
Open Access | Times Cited: 46

Showing 1-25 of 46 citing articles:

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: 91
The pathogenesis of systemic lupus erythematosus: Harnessing big data to understand the molecular basis of lupus
Michelle D. Catalina, Katherine A. Owen, Adam C. Labonte, et al.
Journal of Autoimmunity (2019) Vol. 110, pp. 102359-102359
Closed Access | Times Cited: 135
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
The epilepsy–autism phenotype associated with developmental and epileptic encephalopathies: New mechanism‐based therapeutic options
Nicola Specchio, Valentina Di Micco, Eleonora Aronica, et al.
Epilepsia (2025)
Closed Access | Times Cited: 1
Regulation of neuronal excitation–transcription coupling by Kv2.1-induced clustering of somatic L-type Ca 2+ channels at ER-PM junctions
Nicholas C. Vierra, Samantha C. O’Dwyer, Collin Matsumoto, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 46
Open Access | Times Cited: 38
Potassium channels in behavioral brain disorders. Molecular mechanisms and therapeutic potential: A narrative review
Kazi Asraful Alam, Pernille Svalastoga, Aurora Martı́nez, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 152, pp. 105301-105301
Open Access | Times Cited: 14
De novo KCNB1 missense variant causing developmental and epileptic encephalopathy: Two case reports
Ying Ren, Wandong Hu, Zaifen Gao, et al.
Medicine (2025) Vol. 104, Iss. 2, pp. e41236-e41236
Open Access
Autism Spectrum Disorder and Epilepsy: Pathogenetic Mechanisms and Therapeutic Implications
Alessandra Giliberti, Adele Maria Frisina, Stefania Giustiniano, et al.
Journal of Clinical Medicine (2025) Vol. 14, Iss. 7, pp. 2431-2431
Open Access
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: 32
Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation
Shreyas Bhat, Justine Rousseau, Coralie Michaud, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 4, pp. 761-777
Open Access | Times Cited: 4
Potassium channel‐related epilepsy: Pathogenesis and clinical features
Tong Zhao, Le Wang, Fang Chen
Epilepsia Open (2024) Vol. 9, Iss. 3, pp. 891-905
Open Access | Times Cited: 4
A forward genetic screen identifies potassium channel essentiality in SHH medulloblastoma maintenance
Jerry J. Fan, Anders W. Erickson, Julia Carrillo-García, et al.
Developmental Cell (2025)
Closed Access
Ion Channels Involvement in Neurodevelopmental Disorders
Maria Cristina D’Adamo, Antonella Liantonio, Elena Conte, et al.
Neuroscience (2020) Vol. 440, pp. 337-359
Closed Access | Times Cited: 31
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome
Claire Bar, Mathieu Kuchenbuch, Giulia Barcia, et al.
Epilepsia (2020) Vol. 61, Iss. 11, pp. 2461-2473
Open Access | Times Cited: 31
Mechanism of use-dependent Kv2 channel inhibition by RY785
Matthew James Marquis, Jon T. Sack
The Journal of General Physiology (2022) Vol. 154, Iss. 6
Open Access | Times Cited: 16
Epilepsy and neurobehavioral abnormalities in mice with a dominant-negative KCNB1 pathogenic variant
Nicole A. Hawkins, Sunita N. Misra, Manuel Jurado, et al.
Neurobiology of Disease (2020) Vol. 147, pp. 105141-105141
Open Access | Times Cited: 27
Integrin-KCNB1 potassium channel complexes regulate neocortical neuronal development and are implicated in epilepsy
Alessandro Bortolami, Wei Yu, Elena Forzisi, et al.
Cell Death and Differentiation (2022) Vol. 30, Iss. 3, pp. 687-701
Open Access | Times Cited: 15
Inherited Developmental and Epileptic Encephalopathies
Emanuele Bartolini
Neurology International (2021) Vol. 13, Iss. 4, pp. 555-568
Open Access | Times Cited: 19
Altered neurological and neurobehavioral phenotypes in a mouse model of the recurrent KCNB1-p.R306C voltage-sensor variant
Seok Kyu Kang, Nicole A. Hawkins, Christopher H. Thompson, et al.
Neurobiology of Disease (2024) Vol. 194, pp. 106470-106470
Open Access | Times Cited: 2
Mutant analysis of Kcng4b reveals how the different functional states of the voltage-gated potassium channel regulate ear development
Justyna Jędrychowska, Vitya Vardanyan, Miłosz Wieczór, et al.
Developmental Biology (2024) Vol. 513, pp. 50-62
Open Access | Times Cited: 2
Three different scenarios for epileptic spasms
Lucia Fusco, Domenico Serino, Marta Elena Santarone
Epilepsy & Behavior (2020) Vol. 113, pp. 107531-107531
Closed Access | Times Cited: 18
Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder
Juan Xiong, Zhonghua Liu, Shimeng Chen, et al.
Frontiers in Pediatrics (2022) Vol. 9
Open Access | Times Cited: 11
A KCNB1 gain of function variant causes developmental delay and speech apraxia but not seizures
Emma L. Veale, Alessia Golluscio, Katheryn Grand, et al.
Frontiers in Pharmacology (2022) Vol. 13
Open Access | Times Cited: 11
Ion channels in neurodevelopment: lessons from the Integrin-KCNB1 channel complex
Alessandro Bortolami, Federico Sesti
Neural Regeneration Research (2023) Vol. 18, Iss. 11, pp. 2365-2369
Open Access | Times Cited: 6
Role of Potassium Ion Channels in Epilepsy: Focus on Current Therapeutic Strategies
Rahul Khan, Pragya Chaturvedi, Prachi Sahu, et al.
CNS & Neurological Disorders - Drug Targets (2022) Vol. 23, Iss. 1, pp. 67-87
Closed Access | Times Cited: 10
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