Open Access Helper

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:

Surrogate gene therapy for muscular dystrophy
Kay E. Davies, Jeffrey S. Chamberlain
Nature Medicine (2019) Vol. 25, Iss. 10, pp. 1473-1474
Closed Access | Times Cited: 10

Showing 10 citing articles:

Muscle spindle function in healthy and diseased muscle
Stephan Kröger, Bridgette Watkins
Skeletal Muscle (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 87
Therapy development for spinal muscular atrophy: perspectives for muscular dystrophies and neurodegenerative disorders
Sibylle Jablonka, Luisa Hennlein, Michael Sendtner
Neurological Research and Practice (2022) Vol. 4, Iss. 1
Open Access | Times Cited: 52
Recombinant Adeno-Associated Viral Vectors (rAAV)-Vector Elements in Ocular Gene Therapy Clinical Trials and Transgene Expression and Bioactivity Assays
Thilo M. Buck, Jan Wijnholds
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 12, pp. 4197-4197
Open Access | Times Cited: 70
Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophy
Vratko Himič, Kay E. Davies
European Journal of Human Genetics (2021) Vol. 29, Iss. 9, pp. 1369-1376
Open Access | Times Cited: 35
Impaired muscle spindle function in murine models of muscular dystrophy
Laura Gerwin, Sarah Rossmanith, Corinna Haupt, et al.
The Journal of Physiology (2020) Vol. 598, Iss. 8, pp. 1591-1609
Open Access | Times Cited: 15
Muscular dystrophy: Experimental animal models and therapeutic approaches (Review)
Gisela Găină, Alexandra Popa
Experimental and Therapeutic Medicine (2021) Vol. 21, Iss. 6
Open Access | Times Cited: 10
Targeting IRES-dependent translation as a novel approach for treating Duchenne muscular dystrophy
Christine Péladeau, Bernard J. Jasmin
RNA Biology (2020) Vol. 18, Iss. 9, pp. 1238-1251
Open Access | Times Cited: 4
A Long-Term Study Evaluating the Effects of Nicorandil Treatment on Duchenne Muscular Dystrophy-Associated Cardiomyopathy in mdx Mice
Melanie Gartz, Margaret Haberman, Mariah J. Prom, et al.
Journal of Cardiovascular Pharmacology and Therapeutics (2022) Vol. 27
Open Access | Times Cited: 1
L.O. Badalyan and current progress in the study of hereditary neuromuscular diseases
Н. Н. Заваденко, D. Vlodavets
L O Badalyan Neurological Journal (2020) Vol. 1, Iss. 1, pp. 64-72
Open Access | Times Cited: 1
“Micro-utrophin” Gene Therapy Shows Promise for Duchenne Muscular Dystrophy in Animal Models
Richard Robinson
Neurology Today (2019) Vol. 19, Iss. 23, pp. 8-9
Closed Access
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