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:

Duchenne muscular dystrophy: pathogenesis and promising therapies
Mengyuan Chang, Yong Cai, Zihui Gao, et al.
Journal of Neurology (2023) Vol. 270, Iss. 8, pp. 3733-3749
Closed Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

Mitochondrial dysfunction: roles in skeletal muscle atrophy
Xin Chen, Yanan Ji, Ruiqi Liu, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 110

Delandistrogene Moxeparvovec: First Approval
Sheridan M. Hoy
Drugs (2023) Vol. 83, Iss. 14, pp. 1323-1329
Closed Access | Times Cited: 91

β2-Adrenergic Regulation of the Neuromuscular Transmission and Its Lipid-Dependent Switch
Chulpan R. Gafurova, Andrei N. Tsentsevitsky, Nikita S. Fedorov, et al.
Molecular Neurobiology (2024) Vol. 61, Iss. 9, pp. 6805-6821
Closed Access | Times Cited: 9

MuSCs and IPCs: roles in skeletal muscle homeostasis, aging and injury
Haiyan Jiang, Boya Liu, Junfei Lin, et al.
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 8

Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X‐linked muscular dystrophy in a cat
G. Diane Shelton, Fabrizio Tucciarone, Ling T. Guo, et al.
Journal of Veterinary Internal Medicine (2024) Vol. 38, Iss. 1, pp. 135-144
Open Access | Times Cited: 6

Oral administration of plumbagin is beneficial in in vivo models of Duchenne muscular dystrophy through control of redox signaling
Davide Cervia, Silvia Zecchini, Luca Pincigher, et al.
Free Radical Biology and Medicine (2024) Vol. 225, pp. 193-207
Open Access | Times Cited: 4

Safety and Tolerability of Wharton’s Jelly-Derived Mesenchymal Stem Cells for Patients With Duchenne Muscular Dystrophy: A Phase 1 Clinical Study
Jiwon Lee, Sang Eon Park, Mi‐Ra Kim, et al.
Journal of Clinical Neurology (2025) Vol. 21, Iss. 1, pp. 40-40
Open Access

Stem cell therapy: A promising therapeutic approach for skeletal muscle atrophy
Yingjie Wang, Zehao Chen, Yuntian Shen, et al.
World Journal of Stem Cells (2025) Vol. 17, Iss. 2
Closed Access

Radiomics with Ultrasound Radiofrequency Data for Improving Evaluation of Duchenne Muscular Dystrophy
Dong Yan, Qiang Li, Ya‐Wen Chuang, et al.
Deleted Journal (2025)
Closed Access

Polypharmacology: new drugs in 2023–2024
Piotr Ryszkiewicz, Barbara Malinowska, Eberhard Schlicker
Pharmacological Reports (2025)
Open Access

Advances in Duchenne Muscular Dystrophy: Diagnostic Techniques and Dystrophin Domain Insights
Julija Sarvutiene, Arūnas Ramanavičius, Simonas Ramanavičius, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3579-3579
Open Access

Muscle stem cell dysfunction in rhabdomyosarcoma and muscular dystrophy
Rebecca Robertson, Shulei Li, Romina L. Filippelli, et al.
Current topics in developmental biology/Current Topics in Developmental Biology (2024), pp. 83-121
Closed Access | Times Cited: 3

How Can Proteomics Help to Elucidate the Pathophysiological Crosstalk in Muscular Dystrophy and Associated Multi-System Dysfunction?
Paul Dowling, Capucine Trollet, Elisa Négroni, et al.
Proteomes (2024) Vol. 12, Iss. 1, pp. 4-4
Open Access | Times Cited: 2

Cellular interactions and microenvironment dynamics in skeletal muscle regeneration and disease
Cristina Rodríguez, Filipa Timóteo-Ferreira, Gabriella Minchiotti, et al.
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 1

Revolutionizing genetic diagnostics: Innovative techniques for inherited disease detection
Shradha Devi Dwivedi, Sachin Yadav, Divya Sahu, et al.
Gene Reports (2024) Vol. 36, pp. 101963-101963
Closed Access | Times Cited: 1

Circadian Clock in Muscle Disease Etiology and Therapeutic Potential for Duchenne Muscular Dystrophy
Tali Kiperman, Ke Ma
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4767-4767
Open Access

ECM components are essential for proper in vitro myogenesis
Uğur Akpulat
European Journal of Therapeutics (2024) Vol. 30, Iss. 5, pp. 675-681
Open Access

Genomic insights into Duchene muscular dystrophy: Analysis of 1250 patients reveals 30% novel genetic patterns and 6 novel variants
Khalda Amr, Nagia Fahmy, Ghada El‐Kamah
Journal of Genetic Engineering and Biotechnology (2024) Vol. 22, Iss. 4, pp. 100436-100436
Closed Access

Digital outcome measures in Duchene muscular dystrophy: Lessons learnt from clinical trials
Camila Gonzalez-Barral, Laurent Servais
Journal of Neuromuscular Diseases (2024)
Open Access

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