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:
ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks
Maria W A Teunissen, Elly Lewerissa, Eline van Hugte, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 14, pp. 2373-2385
Open Access | Times Cited: 8
Maria W A Teunissen, Elly Lewerissa, Eline van Hugte, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 14, pp. 2373-2385
Open Access | Times Cited: 8
Showing 8 citing articles:
Ion channel traffic jams: the significance of trafficking deficiency in long QT syndrome
Gema Mondéjar‐Parreño, Ana I. Moreno-Manuel, Juan Manuel Ruiz-Robles, et al.
Cell Discovery (2025) Vol. 11, Iss. 1
Open Access
Gema Mondéjar‐Parreño, Ana I. Moreno-Manuel, Juan Manuel Ruiz-Robles, et al.
Cell Discovery (2025) Vol. 11, Iss. 1
Open Access
Exploratory analysis of a Novel RACK1 mutation and its potential role in epileptic seizures via Microglia activation
Sai Zhang, Zhaofei Dong, Jiafu Ji, et al.
Journal of Neuroinflammation (2025) Vol. 22, Iss. 1
Open Access
Sai Zhang, Zhaofei Dong, Jiafu Ji, et al.
Journal of Neuroinflammation (2025) Vol. 22, Iss. 1
Open Access
Self‐limited familial focal epilepsy caused by ANK2 variants: A potentially under‐recognized condition
Po‐Hsi Lin, Chen‐Jui Ho, Chih‐Hsiang Lin, et al.
Epilepsia Open (2025)
Open Access
Po‐Hsi Lin, Chen‐Jui Ho, Chih‐Hsiang Lin, et al.
Epilepsia Open (2025)
Open Access
A Mutation in the ANK2 Gene Causing ASD and a Review of the Literature
Lu Zhao, Zhidong Qiao, Yue‐Xin Jia, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 3
Open Access
Lu Zhao, Zhidong Qiao, Yue‐Xin Jia, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 3
Open Access
Early developmental deletion of forebrain Ank2 causes seizure-related phenotypes by reshaping the synaptic proteome
Sehyoun Yoon, Marc Dos Santos, Marc P. Forrest, et al.
Cell Reports (2023) Vol. 42, Iss. 7, pp. 112784-112784
Open Access | Times Cited: 5
Sehyoun Yoon, Marc Dos Santos, Marc P. Forrest, et al.
Cell Reports (2023) Vol. 42, Iss. 7, pp. 112784-112784
Open Access | Times Cited: 5
Roles of ANK2/ankyrin-B in neurodevelopmental disorders: Isoform functions and implications for autism spectrum disorder and epilepsy
Sehyoun Yoon, Peter Penzes
Current Opinion in Neurobiology (2024) Vol. 90, pp. 102938-102938
Open Access | Times Cited: 1
Sehyoun Yoon, Peter Penzes
Current Opinion in Neurobiology (2024) Vol. 90, pp. 102938-102938
Open Access | Times Cited: 1
Targeting epigenetic dysregulation in autism spectrum disorders
Macarena L Herrera, Juan Paraíso‐Luna, Isabel Bustos-Martínez, et al.
Trends in Molecular Medicine (2024) Vol. 30, Iss. 11, pp. 1028-1046
Closed Access
Macarena L Herrera, Juan Paraíso‐Luna, Isabel Bustos-Martínez, et al.
Trends in Molecular Medicine (2024) Vol. 30, Iss. 11, pp. 1028-1046
Closed Access
Overabundant endocannabinoids in neurons are detrimental to cognitive function
Dexiao Zhu, Jian Zhang, Xiaokuang Ma, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Dexiao Zhu, Jian Zhang, Xiaokuang Ma, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
