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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:

Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions
Lars Mohren, Friedrich Erdlenbruch, Elsa Leitão, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13

Showing 13 citing articles:

The folding and misfolding of multidomain proteins
Stefano Gianni, Maurizio Brunori
Molecular Aspects of Medicine (2025) Vol. 101, pp. 101337-101337
Closed Access | Times Cited: 1
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
Visualization and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
Wouter De Coster, Ida Höijer, Inge Bruggeman, et al.
Genome Research (2024) Vol. 34, Iss. 11, pp. 2074-2080
Open Access | Times Cited: 4
High Prevalence of the Intronic GAA- FGF14 Repeat Expansion in Dutch Patients With Late-Onset Ataxia
Ana Ignjatijevic, Femke Boorsma, Elles Wierenga, et al.
Neurology Genetics (2025) Vol. 11, Iss. 2
Closed Access
Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders
Eddy N. de Boer, Arjen J. Scheper, Dennis Hendriksen, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 7, pp. 2850-2850
Open Access
The genetic landscape of sporadic adult-onset degenerative ataxia: a multi-modal genetic study of 377 consecutive patients from the longitudinal multi-centre SPORTAX cohort
Danique Beijer, David Mengel, Demet Önder, et al.
EBioMedicine (2025) Vol. 115, pp. 105715-105715
Closed Access
Dietary and lifestyle interventions for the management of hereditary ataxias
Wenyao Yang, Bruce Thompson, Faith Kwa
Frontiers in Nutrition (2025) Vol. 12
Open Access
Spinocerebellar ataxia 27B (SCA27B)—a systematic review and a case report of a Polish family
Adam Sebastian Hirschfeld, Julia O. Misiorek, Magdalena Dabrowska, et al.
Journal of Applied Genetics (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
The FGF14 GAA repeat expansion is a major cause of ataxia in the Cypriot population
Ioannis Livanos, Christina Votsi, Kyriaki Michailidou, et al.
Brain Communications (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 1
FGF14repeat length and mosaic interruptions: modifiers of SCA27b?
Joshua Laß, Mirja Thomsen, Max Borsche, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
No evidence for association between GAA-FGF14 expansion and early onset cerebellar ataxia: a study on 85 undiagnosed patients
Clarisse Delvallée, Nadège Calmels, Thomas Bogdan, et al.
Journal of Neurology (2024) Vol. 272, Iss. 1
Closed Access
Enhanced detection and genotyping of disease-associated tandem repeats using HMMSTR and targeted long-read sequencing
Kinsey Van Deynze, Camille Mumm, Connor J. Maltby, et al.
Nucleic Acids Research (2024)
Open Access
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