Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease
Joel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
The American Journal of Human Genetics (2023) Vol. 111, Iss. 1, pp. 82-95
Open Access | Times Cited: 48

Showing 1-25 of 48 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: 16
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: 12
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
Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategies
Elsa Leitão, Christopher Schröder, Christel Depienne
Revue Neurologique (2024) Vol. 180, Iss. 5, pp. 383-392
Open Access | Times Cited: 9
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
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: 9
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: 5
Short Tandem Repeats in the era of next-generation sequencing: from historical loci to population databases
Kévin Uguen, Jacques L. Michaud, Emmanuelle Génin
European Journal of Human Genetics (2024) Vol. 32, Iss. 9, pp. 1037-1044
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
Zinc finger homeobox-3 (ZFHX3) orchestrates genome-wide daily gene expression in the suprachiasmatic nucleus
Akanksha Bafna, Gareth Banks, V. B. Vasilyev, et al.
(2025)
Open Access
Zinc finger homeobox-3 (ZFHX3) orchestrates genome-wide daily gene expression in the suprachiasmatic nucleus
Akanksha Bafna, Gareth Banks, V. B. Vasilyev, et al.
(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
Demystifying the Etiology of ILOCA in the Genomic Era: A Narrative Review
Luiz Eduardo Novis, Thiago Yoshinaga Tonholo Silva, José Luiz Pedroso, et al.
The Cerebellum (2025) Vol. 24, Iss. 2
Closed Access
Recent progress in oculopharyngodistal myopathy research from clinical and genetic viewpoints
Hiroyuki Ishiura
Journal of Neuromuscular Diseases (2025)
Open Access
Zinc finger homeobox-3 (ZFHX3) orchestrates genome-wide daily gene expression in the suprachiasmatic nucleus
Akanksha Bafna, Gareth Banks, V. B. Vasilyev, et al.
(2025)
Open Access
ONT in Clinical Diagnostics of Repeat Expansion Disorders: Detection and Reporting Challenges
Ludmila Kaplun, Greice Krautz‐Peterson, Nir Neerman, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 6, pp. 2725-2725
Open Access
Zinc finger homeobox-3 (ZFHX3) orchestrates genome-wide daily gene expression in the suprachiasmatic nucleus
Akanksha Bafna, Gareth Banks, V. B. Vasilyev, et al.
eLife (2025) Vol. 14
Open Access
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
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
Barriers to clinical genetic testing in movement disorders
Dennis Yeow, Laura Ivete Rudaks, Kishore R. Kumar
Current Opinion in Neurology (2025)
Closed Access
Page 1 - Next Page

Scroll to top