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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:

Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of view
Giulia Coarelli, Alexis Brice, Alexandra Dürr
F1000Research (2018) Vol. 7, pp. 1781-1781
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

Do Post-Translational Modifications Influence Protein Aggregation in Neurodegenerative Diseases: A Systematic Review
Larissa-Nele Schaffert, Wayne G. Carter
Brain Sciences (2020) Vol. 10, Iss. 4, pp. 232-232
Open Access | Times Cited: 130
Substantia nigra degeneration in spinocerebellar ataxia 2 and 7 using neuromelanin‐sensitive imaging
Lydia Chougar, Giulia Coarelli, François‐Xavier Lejeune, et al.
European Journal of Neurology (2025) Vol. 32, Iss. 1
Open Access | Times Cited: 1
Spinocerebellar ataxia clinical trials: opportunities and challenges
Sarah M. Brooker, Chandrakanth Reddy Edamakanti, Sara M. Akasha, et al.
Annals of Clinical and Translational Neurology (2021) Vol. 8, Iss. 7, pp. 1543-1556
Open Access | Times Cited: 46
Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia
Annika Thierfelder, Jens Seemann, Natalie John, et al.
Movement Disorders (2022) Vol. 37, Iss. 5, pp. 1047-1058
Open Access | Times Cited: 33
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families
Maria Lieto, Vittorio Riso, Daniele Galatolo, et al.
European Journal of Neurology (2019) Vol. 27, Iss. 3, pp. 498-505
Closed Access | Times Cited: 54
Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2
Polina A. Egorova, Ilya Bezprozvanny
Neurotherapeutics (2019) Vol. 16, Iss. 4, pp. 1050-1073
Open Access | Times Cited: 45
Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7
Anna Niewiadomska-Cimicka, Yvon Trottier
Neurotherapeutics (2019) Vol. 16, Iss. 4, pp. 1074-1096
Open Access | Times Cited: 41
Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism
Fanny Casse, Thomas Courtin, Christelle Tesson, et al.
Movement Disorders Clinical Practice (2023) Vol. 10, Iss. 4, pp. 664-669
Open Access | Times Cited: 12
Phenotypic variability in cases with CACNA1A mutation
Sema Bozkaya Yılmaz, Nihal Olgaç Dündar, Nargiz Aliyeva, et al.
European Journal of Pediatrics (2025) Vol. 184, Iss. 4
Open Access
Collaborative Efforts for Spinocerebellar Ataxia Research in the United States: CRC-SCA and READISCA
Chih-Chun Lin, Tetsuo Ashizawa, Sheng‐Han Kuo
Frontiers in Neurology (2020) Vol. 11
Open Access | Times Cited: 29
Pharmacological and non-pharmacological management of spinocerebellar ataxia: A systematic review
Kah Hui Yap, Shahrul Azmin, Jemaima Che Hamzah, et al.
Journal of Neurology (2021) Vol. 269, Iss. 5, pp. 2315-2337
Closed Access | Times Cited: 25
Spinocerebellar ataxias: from pathogenesis to recent therapeutic advances
Zi-Ting Cui, Zong-Tao Mao, Rong Yang, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access | Times Cited: 3
Exosomes as Biomarkers and Therapeutic Agents in Neurodegenerative Diseases: Current Insights and Future Directions
Sam Dehghani, Ozgecan Ocakcı, Pars Tan Hatipoglu, et al.
Molecular Neurobiology (2025)
Open Access
Neuroradiological Findings in the Spinocerebellar Ataxias.
Alex Tiburtino Meira, Walter Oleschko Arruda, Sergio Eiji Ono, et al.
PubMed (2019) Vol. 9
Closed Access | Times Cited: 27
Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review
Jun Young Park, Kwangsic Joo, Se Joon Woo
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 26
Myelinating Glia: Potential Therapeutic Targets in Polyglutamine Spinocerebellar Ataxias
Alexandra F. Putka, Juan P. Mato, Hayley S. McLoughlin
Cells (2023) Vol. 12, Iss. 4, pp. 601-601
Open Access | Times Cited: 9
Current Status of Gene Therapy Research in Polyglutamine Spinocerebellar Ataxias
Ricardo Afonso-Reis, Inês T. Afonso, Clévio Nóbrega
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 4249-4249
Open Access | Times Cited: 18
Dancing, Lurching and Swaying: An Indian Case of Dentatorubral—Pallidoluysian Atrophy
Koustubh Bavdhankar, Neeraj Jain, Mayur Thakkar, et al.
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. S2
Closed Access | Times Cited: 2
DRPLA: understanding the natural history and developing biomarkers to accelerate therapeutic trials in a globally rare repeat expansion disorder
Aiysha Chaudhry, Alkyoni Anthanasiou-Fragkouli, Henry Houlden
Journal of Neurology (2020) Vol. 268, Iss. 8, pp. 3031-3041
Open Access | Times Cited: 17
Antisense therapies in neurological diseases
J.-B. Brunet de Courssou, Alexandra Dürr, David Adams, et al.
Brain (2021) Vol. 145, Iss. 3, pp. 816-831
Open Access | Times Cited: 15
Heterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population
Szu‐Ju Chen, Ni‐Chung Lee, Yin‐Hsiu Chien, et al.
Brain and Behavior (2019) Vol. 9, Iss. 10
Open Access | Times Cited: 15
Broad Influence of Mutant Ataxin-3 on the Proteome of the Adult Brain, Young Neurons, and Axons Reveals Central Molecular Processes and Biomarkers in SCA3/MJD Using Knock-In Mouse Model
Kalina Wiatr, Łukasz Marczak, J. Pérot, et al.
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 11
Targeting for Success: Demonstrating Proof-of-Concept with Mechanistic Early Phase Clinical Pharmacology Studies for Disease-Modification in Neurodegenerative Disorders
Maurits F. J. M. Vissers, Jules A. A. C. Heuberger, Geert Jan Groeneveld
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 4, pp. 1615-1615
Open Access | Times Cited: 10
A Chinese Family with Digenic TBP/STUB1 Spinocerebellar Ataxia
Liu Lili, Juanjuan Chen, Guogao Zhang, et al.
The Cerebellum (2024) Vol. 23, Iss. 4, pp. 1705-1711
Open Access | Times Cited: 1
Predictive coding and adaptive behavior in patients with genetically determined cerebellar ataxia––A neurophysiology study
Sinem Tunç, Nastasja Baginski, Juliane Lubs, et al.
NeuroImage Clinical (2019) Vol. 24, pp. 102043-102043
Open Access | Times Cited: 9
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