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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:

Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs
Martin Paucar, Daniel Nilsson, Martin Engvall, et al.
Journal of Internal Medicine (2024) Vol. 296, Iss. 3, pp. 234-248
Open Access | Times Cited: 11

Showing 11 citing articles:

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability
María del Rocío Pérez Baca, Eva Jacobs, Lies Vantomme, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 3, pp. 509-528
Open Access | Times Cited: 8
Recent Advances in the Genetics of Ataxias: An Update on Novel Autosomal Dominant Repeat Expansions
David Pellerin, Pablo Iruzubieta, Isaac Xu, et al.
Current Neurology and Neuroscience Reports (2025) Vol. 25, Iss. 1
Closed Access | Times Cited: 1
Detailed tandem repeat allele profiling in 1,027 long-read genomes reveals genome-wide patterns of pathogenicity
Matt C. Danzi, Isaac Xu, Sarah Fazal, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Epidemiology of Autosomal Dominant Spinocerebellar Ataxias in Latin America: A Systematic review and Meta-analysis
Milagros Galecio‐Castillo, Jesus Daniel Gutierrez-Arratia, Alonso Abad-Murillo, et al.
Research Square (Research Square) (2025)
Closed Access
Cerebellar Pathology in Forensic and Clinical Neuroscience
Azhagu Madhavan Sivalingam, Darshitha D Sureshkumar
Ageing Research Reviews (2025), pp. 102697-102697
Closed Access
Recent progress in oculopharyngodistal myopathy research from clinical and genetic viewpoints
Hiroyuki Ishiura
Journal of Neuromuscular Diseases (2025)
Open Access
Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies
Guillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, et al.
Movement Disorders (2025)
Open Access
Epidemiology of Autosomal Dominant Spinocerebellar Ataxias in Latin America: A Systematic Review and Meta-Analysis
Milagros Galecio‐Castillo, Jesus Daniel Gutierrez-Arratia, Alonso Abad-Murillo, et al.
The Cerebellum (2025) Vol. 24, Iss. 3
Closed Access
Decoding the genetic blueprints of neurological disorders: disease mechanisms and breakthrough gene therapies
Umar Saeed, Zahra Zahid Piracha, Muhammad Nouman Tariq, et al.
Frontiers in Neurology (2025) Vol. 16
Open Access
Repeat length in spinocerebellar ataxia type 4 (SCA4) predicts age at onset and disease severity
Andreas Dalski, Martje G. Pauly, Henner Hanssen, et al.
Journal of Neurology (2024) Vol. 271, Iss. 9, pp. 6289-6300
Open Access | Times Cited: 2
The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder
Zhongbo Chen, Pilar Álvarez Jerez, Claire Anderson, et al.
Movement Disorders (2024)
Open Access
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