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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:

Glial Dysfunction and Its Contribution to the Pathogenesis of the Neuronal Ceroid Lipofuscinoses
Keigo Takahashi, Hemanth R. Nelvagal, Jenny Lange, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 16

Showing 16 citing articles:

Open-label evaluation of oral trehalose in patients with neuronal ceroid lipofuscinoses
Stefania Della Vecchia, Nicola Gammaldi, Ivana Ricca, et al.
Journal of Neurology (2025) Vol. 272, Iss. 1
Closed Access | Times Cited: 1
Lipofuscin, Its Origin, Properties, and Contribution to Retinal Fluorescence as a Potential Biomarker of Oxidative Damage to the Retina
Małgorzata Różanowska
Antioxidants (2023) Vol. 12, Iss. 12, pp. 2111-2111
Open Access | Times Cited: 15
Gene therapy ameliorates bowel dysmotility and enteric neuron degeneration and extends survival in lysosomal storage disorder mouse models
Ewa Ziółkowska, Matthew J. Jansen, Letitia L. Williams, et al.
Science Translational Medicine (2025) Vol. 17, Iss. 781
Closed Access
Neuronal Ceroid Lipofuscinosis—Concepts, Classification, and Avenues for Therapy
Yuheng Zhang, Bingying Du, Miaozhan Zou, et al.
CNS Neuroscience & Therapeutics (2025) Vol. 31, Iss. 2
Open Access
Lipofuscin, Its Origin, Properties, and Contribution to Retinal Fluorescence as a Potential Biomarker of Oxidative Damage to the Retina
Małgorzata Różanowska
(2023)
Open Access | Times Cited: 9
TUNEL‐positive structures in activated microglia and SQSTM1/p62‐positive structures in activated astrocytes in the neurodegenerative brain of a CLN10 mouse model
Shun Mitsui, Junji Yamaguchi, Chigure Suzuki, et al.
Glia (2023) Vol. 71, Iss. 12, pp. 2753-2769
Open Access | Times Cited: 8
The involvement of Purkinje cells in progressive myoclonic epilepsy: Focus on neuronal ceroid lipofuscinosis
Sara Bernardi, Federica Gemignani, Maria Marchese
Neurobiology of Disease (2023) Vol. 185, pp. 106258-106258
Open Access | Times Cited: 8
Gene therapy ameliorates spontaneous seizures associated with cortical neuron loss in a Cln2R207X mouse model
Keigo Takahashi, Elizabeth M. Eultgen, Sophie H. Wang, et al.
Journal of Clinical Investigation (2023) Vol. 133, Iss. 12
Open Access | Times Cited: 7
Sex-split analysis of pathology and motor-behavioral outcomes in a mouse model of CLN8-Batten disease reveals an increased disease burden and trajectory in female Cln8mnd mice
Andrew D. Holmes, Katherine A. White, Melissa A. Pratt, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 3
GABAergic interneurons contribute to the fatal seizure phenotype of CLN2 disease mice
Keigo Takahashi, Nicholas Rensing, Elizabeth M. Eultgen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Biochemical, Biomarker, and Behavioral Characterization of the GrnR493X Mouse Model of Frontotemporal Dementia
Denise M. Smith, Geetika Aggarwal, Michael L. Niehoff, et al.
Molecular Neurobiology (2024) Vol. 61, Iss. 11, pp. 9708-9722
Closed Access
Neuronal lipofuscinosis caused by Kufs disease/CLN4DNAJC5mutations but not by a CSPα/DNAJC5 deficiency
Santiago López-Begines, Ángela Lavado-Roldán, Cristina Mesa-Cruz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Biochemical, biomarker, and behavioral characterization of theGrnR493Xmouse model of frontotemporal dementia
Denise M. Smith, Geetika Aggarwal, Michael L. Niehoff, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Bowel dysmotility and enteric neuron degeneration in lysosomal storage disease mice is prevented by gene therapy
Matthew J. Jansen, Letitia L. Williams, Sophie H. Wang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Other diseases of the CNS
Alexei Verkhratsky, Arthur M. Butt
Neuroglia (2023), pp. 629-672
Open Access
Sortilin inhibition treats multiple neurodegenerative lysosomal storage disorders
Hannah Leppert, Joelle T. Anderson, Kaylie J. Timm, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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