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:

Early molecular layer interneuron hyperactivity triggers Purkinje neuron degeneration in SCA1
Federica Pilotto, Christopher Douthwaite, Rim Diab, et al.
Neuron (2023) Vol. 111, Iss. 16, pp. 2523-2543.e10
Open Access | Times Cited: 13

Showing 13 citing articles:

Targeting synapse function and loss for treatment of neurodegenerative diseases
Borislav Dejanovic, Morgan Sheng, Jesse E. Hanson
Nature Reviews Drug Discovery (2023) Vol. 23, Iss. 1, pp. 23-42
Closed Access | Times Cited: 45

Mitochondrial damage and impaired mitophagy contribute to disease progression in SCA6
Tsz Chui Sophia Leung, Eviatar Fields, Namrata Rana, et al.
Acta Neuropathologica (2024) Vol. 147, Iss. 1
Open Access | Times Cited: 7

Hereditary Ataxias: From Bench to Clinic, Where Do We Stand?
Federica Pilotto, Andrea Del Bondio, Hélène Puccio
Cells (2024) Vol. 13, Iss. 4, pp. 319-319
Open Access | Times Cited: 5

Advances in physiological and clinical relevance of hiPSC-derived brain models for precision medicine pipelines
Negin Imani Farahani, Lisa Lin, Shama Nazir, et al.
Frontiers in Cellular Neuroscience (2025) Vol. 18
Open Access

Resilience to Endoplasmic Reticulum Stress Mitigates Calcium-Dependent Membrane Hyperexcitability Underlying Late Disease Onset in SCA6
Haoran Huang, Taylor L. Charron, Min Fu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access

Dysregulation of zebrin-II cell subtypes in the cerebellum is a shared feature across polyglutamine ataxia mouse models and patients
Luke C. Bartelt, Paweł M. Świtoński, Grażyna Adamek, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 772
Closed Access | Times Cited: 3

The Role of Protein Quantity Control in Polyglutamine Spinocerebellar Ataxias
Hongfeng Zhang, Xin Wang
The Cerebellum (2024) Vol. 23, Iss. 6, pp. 2575-2592
Closed Access | Times Cited: 2

Revisiting the development of cerebellar inhibitory interneurons in the light of single-cell genetic analyses
Karl Schilling
Histochemistry and Cell Biology (2023) Vol. 161, Iss. 1, pp. 5-27
Open Access | Times Cited: 4

Probing cerebellar circuit dysfunction in rodent models of spinocerebellar ataxia by means of in vivo two-photon calcium imaging
Christopher Douthwaite, Christoph Tietje, XiaoQian Ye, et al.
STAR Protocols (2024) Vol. 5, Iss. 1, pp. 102911-102911
Open Access

Generation and enrichment of cerebellar GABAergic interneurons from human induced pluripotent stem cells and intracellular calcium measurements
Federica Pilotto, Rim Diab, Zahraa Al qassab, et al.
STAR Protocols (2024) Vol. 5, Iss. 2, pp. 102936-102936
Open Access

Emerging insights into the function of very long chain fatty acids at cerebellar synapses
Martin‐Paul Agbaga, Mohiuddin Ahmad
Neural Regeneration Research (2024) Vol. 20, Iss. 6, pp. 1709-1710
Open Access

Hereditary Ataxias: From Bench to Clinic, where Do We Stand?
Federica Pilotto, Andrea Del Bondio, Hélène Puccio
(2023)
Open Access | Times Cited: 1

Spinocerebellar ataxia type 1: It’s not just about Purkinje cells
Puneet Opal
Neuron (2023) Vol. 111, Iss. 16, pp. 2461-2462
Closed Access

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