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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:

Recent insights into neuromuscular junction biology in Duchenne muscular dystrophy: Impacts, challenges, and opportunities
Sean Y. Ng, Vladimir Ljubicic
EBioMedicine (2020) Vol. 61, pp. 103032-103032
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

The Neuromuscular Junction: Roles in Aging and Neuromuscular Disease
Shama R. Iyer, Sameer B. Shah, Richard M. Lovering
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 15, pp. 8058-8058
Open Access | Times Cited: 65
Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
Massimo Ganassi, Peter S. Zammit
European Journal of Translational Myology (2022) Vol. 32, Iss. 1
Open Access | Times Cited: 58
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: 27
ACE Inhibitors Improve Skeletal Muscle by Preserving Neuromuscular Junctions in Patients with Alzheimer’s Disease
Rizwan Qaisar, Asima Karim, M. Shahid Iqbal, et al.
Journal of Alzheimer s Disease (2023) Vol. 94, Iss. 2, pp. 641-650
Closed Access | Times Cited: 17
The Dystrophin Node as Integrator of Cytoskeletal Organization, Lateral Force Transmission, Fiber Stability and Cellular Signaling in Skeletal Muscle
Paul Dowling, Stephen Gargan, Sandra Murphy, et al.
Proteomes (2021) Vol. 9, Iss. 1, pp. 9-9
Open Access | Times Cited: 36
Complexity of skeletal muscle degeneration: multi-systems pathophysiology and organ crosstalk in dystrophinopathy
Kay Ohlendieck, Dieter Swandulla
Pflügers Archiv - European Journal of Physiology (2021) Vol. 473, Iss. 12, pp. 1813-1839
Open Access | Times Cited: 33
Heterogeneous Skeletal Muscle Cell and Nucleus Populations Identified by Single-Cell and Single-Nucleus Resolution Transcriptome Assays
Katherine Williams, Kyoko Yokomori, A Mortazavi
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 26
AMPK is mitochondrial medicine for neuromuscular disorders
Andrew I. Mikhail, Sean Y. Ng, Stephanie R. Mattina, et al.
Trends in Molecular Medicine (2023) Vol. 29, Iss. 7, pp. 512-529
Open Access | Times Cited: 11
Disruption of Neuromuscular Junction Following Spinal Cord Injury and Motor Neuron Diseases
Colin Nemeth, Naren L. Banik, Azizul Haque
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 6, pp. 3520-3520
Open Access | Times Cited: 4
Therapeutic aspects of cell signaling and communication in Duchenne muscular dystrophy
Alicja Starosta, Patryk Konieczny
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 11, pp. 4867-4891
Open Access | Times Cited: 27
Synaptic alterations as a neurodevelopmental trait of Duchenne muscular dystrophy
Maria Egle De Stefano, Valentina Ferretti, Chiara Mozzetta
Neurobiology of Disease (2022) Vol. 168, pp. 105718-105718
Open Access | Times Cited: 18
Histological Methods to Assess Skeletal Muscle Degeneration and Regeneration in Duchenne Muscular Dystrophy
Nicolas Dubuisson, Romain Versele, Chloé Planchon, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 24, pp. 16080-16080
Open Access | Times Cited: 17
Respiratory pathology in the mdx/utrn -/- mouse: A murine model for Duchenne Muscular Dystrophy (DMD)
Marán Y. Hernández Rodríguez, Debolina D. Biswas, Aoife D. Slyne, et al.
PLoS ONE (2025) Vol. 20, Iss. 2, pp. e0316295-e0316295
Open Access
Mimicking the Dystrophic Cardiac Extracellular Environment through DystroGel
Maila Chirivì, Fabio Maiullari, Marika Milan, et al.
Advanced Healthcare Materials (2025)
Open Access
The necessity for skeletal muscle contractile assays to assess treatment efficacy in DMD
Chia-Yi Yuan, Amanda Sweeten, Robert W. Grange
Rare Disease and Orphan Drugs Journal (2025) Vol. 4, Iss. 1
Open Access
Volitional exercise elicits physiological and molecular improvements in the severe D2.mdx mouse model of Duchenne muscular dystrophy
Stephanie R. Mattina, Sean Y. Ng, Andrew I. Mikhail, et al.
The Journal of Physiology (2025)
Open Access
Functional specialisation and coordination of myonuclei
Amaury Korb, Shahragim Tajbakhsh, Glenda Comai
Biological reviews/Biological reviews of the Cambridge Philosophical Society (2024) Vol. 99, Iss. 4, pp. 1164-1195
Closed Access | Times Cited: 3
Optogenetic modeling of human neuromuscular circuits in Duchenne muscular dystrophy with CRISPR and pharmacological corrections
Amaia Paredes‐Redondo, Peter Harley, Eleni Maniati, et al.
Science Advances (2021) Vol. 7, Iss. 37
Open Access | Times Cited: 17
Dystrophic Muscle Affects Motoneuron Axon Outgrowth and NMJ Assembly
Ersilia Fornetti, Stefano Testa, Francesca De Paolis, et al.
Advanced Materials Technologies (2022) Vol. 7, Iss. 7
Open Access | Times Cited: 12
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
Increasing LRP4 diminishes neuromuscular deficits in a mouse model of Duchenne muscular dystrophy
Tiankun Hui, Hongyang Jing, Tian Zhou, et al.
Human Molecular Genetics (2021) Vol. 30, Iss. 17, pp. 1579-1590
Open Access | Times Cited: 14
Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy
Elisabeth A. Kilroy, Amanda C Ignacz, Kaylee L Brann, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 10
Regeneration mechanisms and therapeutic strategies for neuromuscular junctions in aging and diseases
Masashi Fujitani, Abu Md Mamun Tarif, Yoshinori Otani
Neural Regeneration Research (2024) Vol. 20, Iss. 1, pp. 193-194
Open Access | Times Cited: 1
Older mice show decreased regeneration of neuromuscular junctions following lengthening contraction-induced injury
Thomas A. Paul, Peter Macpherson, Tara L. Janetzke, et al.
GeroScience (2023) Vol. 45, Iss. 3, pp. 1899-1912
Open Access | Times Cited: 2
Sensitivity of subcellular components of neuromuscular junctions to decreased neuromuscular activity
Michael R. Deschenes, Audrey M. Trebelhorn, Madeline C. High, et al.
Synapse (2021) Vol. 75, Iss. 11
Closed Access | Times Cited: 4
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