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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:

RNA toxicity and foci formation in microsatellite expansion diseases
Nan Zhang, Tetsuo Ashizawa
Current Opinion in Genetics & Development (2017) Vol. 44, pp. 17-29
Open Access | Times Cited: 96

Showing 1-25 of 96 citing articles:

Spinocerebellar ataxia
Thomas Klockgether, Caterina Mariotti, Henry L. Paulson
Nature Reviews Disease Primers (2019) Vol. 5, Iss. 1
Closed Access | Times Cited: 534
Repeat expansion diseases
Henry L. Paulson
Handbook of clinical neurology (2018), pp. 105-123
Open Access | Times Cited: 374
Molecular mechanisms underlying nucleotide repeat expansion disorders
Indranil Malik, Chase P. Kelley, Eric T. Wang, et al.
Nature Reviews Molecular Cell Biology (2021) Vol. 22, Iss. 9, pp. 589-607
Open Access | Times Cited: 263
Cellular origins of dsRNA, their recognition and consequences
Y. Grace Chen, Sun Hur
Nature Reviews Molecular Cell Biology (2021) Vol. 23, Iss. 4, pp. 286-301
Open Access | Times Cited: 256
Bridging biophysics and neurology: aberrant phase transitions in neurodegenerative disease
Natalia B. Nedelsky, J. Paul Taylor
Nature Reviews Neurology (2019) Vol. 15, Iss. 5, pp. 272-286
Closed Access | Times Cited: 187
An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics
Sanjog R. Chintalaphani, Sandy S. Pineda, Ira W. Deveson, et al.
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 128
Alternative splicing in neurodegenerative disease and the promise of RNA therapies
David Nikom, Sika Zheng
Nature reviews. Neuroscience (2023) Vol. 24, Iss. 8, pp. 457-473
Closed Access | Times Cited: 85
Sequencing and characterizing short tandem repeats in the human genome
Hope A. Tanudisastro, Ira W. Deveson, Harriet Dashnow, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 7, pp. 460-475
Closed Access | Times Cited: 45
Targeting RNA in mammalian systems with small molecules
Anita Donlic, Amanda E. Hargrove
Wiley Interdisciplinary Reviews - RNA (2018) Vol. 9, Iss. 4
Open Access | Times Cited: 120
Intron retention induced by microsatellite expansions as a disease biomarker
Łukasz J. Sznajder, James D. Thomas, Ellie M. Carrell, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 16, pp. 4234-4239
Open Access | Times Cited: 114
Of Men and Mice: Modeling the Fragile X Syndrome
Regina Dahlhaus
Frontiers in Molecular Neuroscience (2018) Vol. 11
Open Access | Times Cited: 113
A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism
Ana Westenberger, Charles Jourdan Reyes, Gerard Saranza, et al.
Annals of Neurology (2019) Vol. 85, Iss. 6, pp. 812-822
Closed Access | Times Cited: 81
Neurodegenerative diseases: a hotbed for splicing defects and the potential therapies
Dunhui Li, Craig S. McIntosh, Frank Mastaglia, et al.
Translational Neurodegeneration (2021) Vol. 10, Iss. 1
Open Access | Times Cited: 73
Nematode chromosomes
Peter M. Carlton, Richard E. Davis, Shawn Ahmed
Genetics (2022) Vol. 221, Iss. 1
Open Access | Times Cited: 42
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1
Zhidong Cen, Zhengwen Jiang, You Chen, et al.
Brain (2018) Vol. 141, Iss. 8, pp. 2280-2288
Open Access | Times Cited: 80
Rethinking Unconventional Translation in Neurodegeneration
Fen‐Biao Gao, Joel D. Richter, Don W. Cleveland
Cell (2017) Vol. 171, Iss. 5, pp. 994-1000
Open Access | Times Cited: 64
Architectural RNAs for Membraneless Nuclear Body Formation
Tomohiro Yamazaki, Shinichi Nakagawa, Tetsuro Hirose
Cold Spring Harbor Symposia on Quantitative Biology (2019) Vol. 84, pp. 227-237
Open Access | Times Cited: 59
Unravelling the enigma of cortical tremor and other forms of cortical myoclonus
Anna Latorre, Lorenzo Rocchi, Francesca Magrinelli, et al.
Brain (2020) Vol. 143, Iss. 9, pp. 2653-2663
Open Access | Times Cited: 53
Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease
Jianwen Deng, Binbin Zhou, Jiaxi Yu, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 5, pp. 462-469
Closed Access | Times Cited: 48
Negative autoregulation mitigates collateral RNase activity of repeat-targeting CRISPR-Cas13d in mammalian cells
Chase P. Kelley, Maja C. Haerle, Eric T. Wang
Cell Reports (2022) Vol. 40, Iss. 7, pp. 111226-111226
Open Access | Times Cited: 38
The polyG diseases: a new disease entity
Tongling Liufu, Yilei Zheng, Jiaxi Yu, et al.
Acta Neuropathologica Communications (2022) Vol. 10, Iss. 1
Open Access | Times Cited: 29
RNA biology of disease-associated microsatellite repeat expansions
Kushal J. Rohilla, Keith T. Gagnon
Acta Neuropathologica Communications (2017) Vol. 5, Iss. 1
Open Access | Times Cited: 61
Therapeutic Genome Editing for Myotonic Dystrophy Type 1 Using CRISPR/Cas9
Yanlin Wang, Hao Lei, Hongcai Wang, et al.
Molecular Therapy (2018) Vol. 26, Iss. 11, pp. 2617-2630
Open Access | Times Cited: 55
Molecular Mechanisms and Therapeutics for the GAA·TTC Expansion Disease Friedreich Ataxia
Joel Gottesfeld
Neurotherapeutics (2019) Vol. 16, Iss. 4, pp. 1032-1049
Open Access | Times Cited: 50
Differential fates of introns in gene expression due to global alternative splicing
Anjani Kumari, Saam Sedehizadeh, J. David Brook, et al.
Human Genetics (2021) Vol. 141, Iss. 1, pp. 31-47
Open Access | Times Cited: 41
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