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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.

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Showing 11 citing articles:

Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications
Indhu‐Shree Rajan‐Babu, Egor Dolzhenko, Michael A. Eberle, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 7, pp. 476-499
Closed Access | Times Cited: 26
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: 14
The impact of interrupted ATXN10 expansions on clinical findings of spinocerebellar ataxia type 10
Ali Hasan, Gabriel Vasata Furtado, Elaine Cristina Miglorini, et al.
Journal of Neurology (2025) Vol. 272, Iss. 4
Closed Access
Spinocerebellar Ataxia Type 10 (SCA 10) in Brazil
Hélio Afonso Ghizoni Teive, Léo Coutinho, Carlos Henrique Ferreira Camargo
The Cerebellum (2025) Vol. 24, Iss. 4
Closed Access
Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitability
Christel Depienne, Arn M. J. M. van den Maagdenberg, Theresa Kühnel, et al.
Epilepsia (2023) Vol. 64, Iss. S1
Open Access | Times Cited: 10
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
An Updated Canvas of the RFC1-mediated CANVAS (Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome)
Sakshi Shukla, Kanav Gupta, Krishna Singh, et al.
Molecular Neurobiology (2024)
Closed Access | Times Cited: 2
Extended haplotype with rs41524547-G defines the ancestral origin of SCA10
Karen N. McFarland, Anjana Tiwari, Vera I. Hashem, et al.
Human Molecular Genetics (2024) Vol. 33, Iss. 18, pp. 1567-1574
Closed Access | Times Cited: 1
Deep learning-enhanced R-loop prediction provides mechanistic implications for repeat expansion diseases
Jiyun Hu, Zetong Xing, Hongbing Yang, et al.
iScience (2024) Vol. 27, Iss. 8, pp. 110584-110584
Open Access
Spinocerebellar ataxia type 10 and Huntington disease‐like 2 in Venezuela: Further evidence of two different ancestral founder effects
Irene Paradisi, Sergio Arias, Vassiliki Ikonomu
Annals of Human Genetics (2024)
Open Access
Pentanucleotide repeat‐related disorders: Genetics and bioinformatic discovery and detection
Isabel Silveira, Mark F. Bennett
Epilepsia (2023) Vol. 64, Iss. S1
Open Access
Understanding functions of eEF1 translation elongation factors beyond translation. A proteomic approach
B. S. Negrutskii, L. V. Porubleva, Agata Malinowska, et al.
Advances in protein chemistry and structural biology (2023)
Closed Access
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