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:

Treatment of Type 1 Myotonic Dystrophy by Engineering Site-specific RNA Endonucleases that Target (CUG)n Repeats
Wenjing Zhang, Yang Wang, Shuyun Dong, et al.
Molecular Therapy (2013) Vol. 22, Iss. 2, pp. 312-320
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

Elimination of Toxic Microsatellite Repeat Expansion RNA by RNA-Targeting Cas9
Ranjan Batra, David A. Nelles, Elaine Pirie, et al.
Cell (2017) Vol. 170, Iss. 5, pp. 899-912.e10
Open Access | Times Cited: 235

Treating pediatric neuromuscular disorders: The future is now
James J. Dowling, Hernán Gonorazky, Ronald D. Cohn, et al.
American Journal of Medical Genetics Part A (2017) Vol. 176, Iss. 4, pp. 804-841
Open Access | Times Cited: 115

Harnessing CRISPR/Cas systems for programmable transcriptional and post-transcriptional regulation
Ahmed Mahas, C. Neal Stewart, Magdy M. Mahfouz
Biotechnology Advances (2017) Vol. 36, Iss. 1, pp. 295-310
Closed Access | Times Cited: 106

Congenital and childhood myotonic dystrophy: Current aspects of disease and future directions
Genevieve Ho
World Journal of Clinical Pediatrics (2015) Vol. 4, Iss. 4, pp. 66-66
Open Access | Times Cited: 103

An Overview of Alternative Splicing Defects Implicated in Myotonic Dystrophy Type I
Andrea López‐Martínez, Patricia Soblechero‐Martín, Laura de la Puente Ovejero, et al.
Genes (2020) Vol. 11, Iss. 9, pp. 1109-1109
Open Access | Times Cited: 95

Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells
Sumitava Dastidar, Simon Ardui, Kshitiz Singh, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. 16, pp. 8275-8298
Open Access | Times Cited: 85

RNA-Binding Proteins: Splicing Factors and Disease
Alger M. Fredericks, Kamil J. Cygan, Brian Brown, et al.
Biomolecules (2015) Vol. 5, Iss. 2, pp. 893-909
Open Access | Times Cited: 87

PPR-SMR protein SOT1 has RNA endonuclease activity
Wen Zhou, Qingtao Lu, Qingwei Li, et al.
Proceedings of the National Academy of Sciences (2017) Vol. 114, Iss. 8
Open Access | Times Cited: 84

Gene Therapy for the Nervous System: Challenges and New Strategies
Casey A. Maguire, Servio H. Ramirez, Steven F. Merkel, et al.
Neurotherapeutics (2014) Vol. 11, Iss. 4, pp. 817-839
Open Access | Times Cited: 83

Genome engineering: a new approach to gene therapy for neuromuscular disorders
Christopher E. Nelson, Jacqueline N. Robinson-Hamm, Charles A. Gersbach
Nature Reviews Neurology (2017) Vol. 13, Iss. 11, pp. 647-661
Closed Access | Times Cited: 66

Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 Mice
Mirella Lo Scrudato, Karine Poulard, Célia Sourd, et al.
Molecular Therapy (2019) Vol. 27, Iss. 8, pp. 1372-1388
Open Access | Times Cited: 46

RNA-mediated therapies in myotonic dystrophy
Sarah J. Overby, Estefanía Cerro-Herreros, Beatriz Llamusí, et al.
Drug Discovery Today (2018) Vol. 23, Iss. 12, pp. 2013-2022
Open Access | Times Cited: 43

Myotonic Dystrophy and Developmental Regulation of RNA Processing
James D. Thomas, Ruan Oliveira, Łukasz J. Sznajder, et al.
Comprehensive physiology (2018), pp. 509-553
Open Access | Times Cited: 39

Expanding RNA binding specificity and affinity of engineered PUF domains
Yangyang Zhao, Miaowei Mao, Wenjing Zhang, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. 9, pp. 4771-4782
Open Access | Times Cited: 37

Applications of Cas9 as an RNA‐programmed RNA‐binding protein
David A. Nelles, Mark Y. Fang, Stefan Aigner, et al.
BioEssays (2015) Vol. 37, Iss. 7, pp. 732-739
Open Access | Times Cited: 35

Pentatricopeptide repeat protein targeting CUG repeat RNA ameliorates RNA toxicity in a myotonic dystrophy type 1 mouse model
Takayoshi Imai, Masahiro Miyai, Joe Nemoto, et al.
Science Translational Medicine (2025) Vol. 17, Iss. 794
Closed Access

Myotonic disorders: A review article.
Christopher N Hahn, Mohammad Salajegheh
PubMed (2016) Vol. 15, Iss. 1, pp. 46-53
Closed Access | Times Cited: 31

Engineering RNA‐binding proteins with diverse activities
Huanhuan Wei, Zefeng Wang
Wiley Interdisciplinary Reviews - RNA (2015) Vol. 6, Iss. 6, pp. 597-613
Closed Access | Times Cited: 30

Structures of RNA repeats associated with neurological diseases
Leszek Błaszczyk, W. Rypniewski, Agnieszka Kiliszek
Wiley Interdisciplinary Reviews - RNA (2017) Vol. 8, Iss. 4
Closed Access | Times Cited: 30

Myospreader improves gene editing in skeletal muscle by myonuclear propagation
Kiril Poukalov, M. Carmen Valero, Derek R. Muscato, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 19
Open Access | Times Cited: 3

Cell Membrane Integrity in Myotonic Dystrophy Type 1: Implications for Therapy
Anchel González-Barriga, Julia Kranzen, Huib J. E. Croes, et al.
PLoS ONE (2015) Vol. 10, Iss. 3, pp. e0121556-e0121556
Open Access | Times Cited: 25

Collagen Nanofibers Facilitated Presynaptic Maturation in Differentiated Neurons from Spinal-Cord-Derived Neural Stem Cells through MAPK/ERK1/2-Synapsin I Signaling Pathway
Yanling Yin, Peng Huang, Zhu Han, et al.
Biomacromolecules (2014) Vol. 15, Iss. 7, pp. 2449-2460
Closed Access | Times Cited: 25

The potential of engineered eukaryotic RNA‐binding proteins as molecular tools and therapeutics
Carl Shotwell, John D. Cleary, J. Andrew Berglund
Wiley Interdisciplinary Reviews - RNA (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 20

Engineering reprogrammable RNA-binding proteins for study and manipulation of the transcriptome
Zhanar Abil, Huimin Zhao
Molecular BioSystems (2015) Vol. 11, Iss. 10, pp. 2658-2665
Closed Access | Times Cited: 19

Genotype and other determinants of respiratory function in myotonic dystrophy type 1
Ghilas Boussaïd, Karim Wahbi, Pascal Laforêt, et al.
Neuromuscular Disorders (2017) Vol. 28, Iss. 3, pp. 222-228
Closed Access | Times Cited: 19

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