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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:

Adaptive Long‐Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4
Zhongbo Chen, Emil K. Gustavsson, Hannah Macpherson, et al.
Movement Disorders (2024) Vol. 39, Iss. 3, pp. 486-497
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy
Karla P. Figueroa, Caspar Groß, Elena Buena‐Atienza, et al.
Nature Genetics (2024) Vol. 56, Iss. 6, pp. 1080-1089
Closed Access | Times Cited: 25
An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches
Laura Ivete Rudaks, Dennis Yeow, Karl Ng, et al.
The Cerebellum (2024) Vol. 23, Iss. 5, pp. 2152-2168
Open Access | Times Cited: 15
Neurological disorders caused by novel non-coding repeat expansions: clinical features and differential diagnosis
Elisa Vegezzi, Hiroyuki Ishiura, D. Cristopher Bragg, et al.
The Lancet Neurology (2024) Vol. 23, Iss. 7, pp. 725-739
Closed Access | Times Cited: 11
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
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
Targeted Long‐Read Sequencing as a Single Assay Improves the Diagnosis of Spastic‐Ataxia Disorders
Laura Ivete Rudaks, Igor Stevanovski, Dennis Yeow, et al.
Annals of Clinical and Translational Neurology (2025)
Open Access | Times Cited: 1
SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies
Laura Ivete Rudaks, Dennis Yeow, Kishore R. Kumar
Movement Disorders (2024) Vol. 39, Iss. 3, pp. 457-461
Closed Access | Times Cited: 6
Repeat expansion disorders
Zhongbo Chen, Huw R. Morris, James Polke, et al.
Practical Neurology (2024), pp. pn-003938
Closed Access | Times Cited: 4
Transcriptomic analysis of repeat expansion-ataxias uncovers distinct non-neuronal cell type-specific signatures of disease across the human brain
Zhongbo Chen, Amy R. Hicks, Jonathan Brenton, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
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
Polyamines enhance repeat-associated non-AUG translation from CCUG repeats by stabilizing the tertiary structure of RNA
Akihiro Oguro, Takeshi Uemura, Kodai Machida, et al.
Journal of Biological Chemistry (2025) Vol. 301, Iss. 3, pp. 108251-108251
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
Mosaicism in Short Tandem Repeat Disorders: A Clinical Perspective
Rose M. Doss, Susana Lopez-Ignacio, Anna Dischler, et al.
Genes (2025) Vol. 16, Iss. 2, pp. 216-216
Open 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
Hereditary Ataxias in Argentina
Malco Rossi, Marcelo Merello
The Cerebellum (2025) Vol. 24, Iss. 3
Closed Access
The continued promise of genomic technologies and software in neurogenetics
Isaac Xu, Matt C. Danzi, Jacquelyn Raposo, et al.
Journal of Neuromuscular Diseases (2025)
Closed Access
Microsatellite expansions hidden within the human dark genome are translated in novel and toxic proteins causing muscle and neurodegenerative diseases
Nicolas Charlet‐Berguerand, Manon Boivin, Jiaxi Yu, et al.
Research Square (Research Square) (2025)
Closed 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 Next, Next-Generation of Sequencing, Promising to Boost Research and Clinical Practice
Kishore R. Kumar, Mark J. Cowley, Ryan L. Davis
Seminars in Thrombosis and Hemostasis (2024) Vol. 50, Iss. 07, pp. 1039-1046
Closed Access | Times Cited: 1
An unexpected polyglycine route to spinocerebellar ataxia
Nicolas Charlet‐Berguerand
Nature Genetics (2024) Vol. 56, Iss. 6, pp. 1039-1041
Closed Access | Times Cited: 1
Comment to: “SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies”
Martin Paucar, Daniel Nilsson, Martin Engvall, et al.
Movement Disorders (2024) Vol. 39, Iss. 6, pp. 1077-1077
Open Access | Times Cited: 1
Optical genome mapping of structural variants in Parkinson’s disease-related induced pluripotent stem cells
Joanne Trinh, Susen Schaake, Carolin Gabbert, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
Origin and evolution of pentanucleotide repeat expansions at the familial cortical myoclonic tremor with epilepsy type1 - SAMD12 locus
Xinhui Chen, Fan Zhang, Yihua Shi, et al.
European Journal of Human Genetics (2024)
Closed Access
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