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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:

Therapeutic opportunities and clinical outcome measures in Duchenne muscular dystrophy
Giulia Ricci, Luca Bello, Francesca Torri, et al.
Neurological Sciences (2022) Vol. 43, Iss. S2, pp. 625-633
Open Access | Times Cited: 20

Showing 20 citing articles:

Givinostat: First Approval
Yvette N. Lamb
Drugs (2024) Vol. 84, Iss. 7, pp. 849-856
Closed Access | Times Cited: 19
Early Cardiac Dysfunction in Duchenne Muscular Dystrophy: A Case Report and Literature Update
Maria Lupu, Irina Pintilie, Raluca Ioana Teleanu, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1685-1685
Open Access | Times Cited: 1
Longitudinal trajectories of muscle impairments in growing boys with Duchenne muscular dystrophy
Ines Vandekerckhove, Marleen Van den Hauwe, Tijl Dewit, et al.
PLoS ONE (2025) Vol. 20, Iss. 3, pp. e0307007-e0307007
Open Access | Times Cited: 1
N-terminal titin fragment: a non-invasive, pharmacodynamic biomarker for microdystrophin efficacy
J Boehler, Kristy J. Brown, Valeria Ricotti, et al.
Skeletal Muscle (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 5
Muscle weakness but also contractures contribute to the progressive gait pathology in children with DMD: a simulation study
Ines Vandekerckhove, Lars D’Hondt, Dhruv Gupta, et al.
Research Square (Research Square) (2025)
Closed Access
Use of assistive technology to assess distal motor function in subjects with neuromuscular disease
Dominique Vincent-Genod, Sylvain Roche, Aurélie Barrière, et al.
PLOS Digital Health (2025) Vol. 4, Iss. 1, pp. e0000534-e0000534
Open Access
Há declínio da fala e da deglutição na Esclerose Lateral Amiotrófica ao longo de dez anos?
Raquel Emanuele de França Mendes, Ivonaldo Leidson Barbosa Lima, Mário Emílio Teixeira Dourado Júnior, et al.
CoDAS (2025) Vol. 37, Iss. 2
Open Access
Is there a decline in speech and swallowing in Amyotrophic Lateral Sclerosis over ten years?
Raquel Emanuele de França Mendes, Ivonaldo Leidson Barbosa Lima, Mário Emílio Teixeira Dourado Júnior, et al.
CoDAS (2025) Vol. 37, Iss. 2
Open Access
Mechanisms of Cardiomyopathy in Duchenne Muscular Dystrophy: A Study Using Pluripotent Stem Cells Derived from Patients with Severe and Mild Motor Impairment
Yue Chang, X. Ai, Ruo Wu, et al.
Tissue and Cell (2025), pp. 102906-102906
Closed Access
Recomendaciones de expertos para la transición a la vida adulta del paciente con distrofia muscular de Duchenne
Edna Julieth Bobadilla-Quesada, Manuel Huertas-Quiñones, Juan David Lasprilla Tovar, et al.
Revista Ciencias de la Salud (2025) Vol. 23, Iss. Especial, pp. 1-30
Open Access
Muscle weakness but also contractures contribute to the progressive gait pathology in children with Duchenne muscular dystrophy: a simulation study
Ines Vandekerckhove, Lars D’Hondt, Dhruv Gupta, et al.
Journal of NeuroEngineering and Rehabilitation (2025) Vol. 22, Iss. 1
Open Access
Gait classification for growing children with Duchenne muscular dystrophy
Ines Vandekerckhove, Eirini Papageorgiou, Britta Hanssen, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 3
Longitudinal trajectories of muscle impairments in growing boys with Duchenne muscular dystrophy
Ines Vandekerckhove, Marleen Van den Hauwe, Tijl Dewit, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Wearable Inertial Devices in Duchenne Muscular Dystrophy: A Scoping Review
Elisa Panero, Rossella D’Alessandro, Ilaria Cavallina, et al.
Applied Sciences (2023) Vol. 13, Iss. 3, pp. 1268-1268
Open Access | Times Cited: 6
Hybrid QUS Radiomics: A Multimodal-Integrated Quantitative Ultrasound Radiomics for Assessing Ambulatory Function in Duchenne Muscular Dystrophy
Dong Yan, Qiang Li, Chia-Wei Lin, et al.
IEEE Journal of Biomedical and Health Informatics (2023) Vol. 28, Iss. 2, pp. 835-845
Closed Access | Times Cited: 6
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study
Giorgia Coratti, Marika Pane, Claudia Brogna, et al.
Neuromuscular Disorders (2023) Vol. 34, pp. 75-82
Closed Access | Times Cited: 4
Physiological stress improves stem cell modeling of dystrophic cardiomyopathy
Dominic E. Fullenkamp, Alexander B. Willis, Jodi L. Curtin, et al.
Disease Models & Mechanisms (2023) Vol. 17, Iss. 6
Open Access | Times Cited: 3
Consensus concept of modern effective therapy for Duchenne muscular dystrophy
T. A. Gremyakova, S. B. Artemyeva, E. N. Baybarina, et al.
Neuromuscular Diseases (2023) Vol. 13, Iss. 2, pp. 10-19
Open Access | Times Cited: 1
Early Cost-Utility Analysis of Ataluren and Eteplirsen in the Treatment of Duchenne Muscular Dystrophy in Egypt
Zahraa Shehata, Andrew Metry, Hoda Rabea, et al.
Value in Health Regional Issues (2023) Vol. 38, pp. 109-117
Closed Access | Times Cited: 1
Use of assistive technology to assess distal motor function in subjects with neuromuscular disease
Dominique Vincent-Genod, Sylvain Roche, Aurélie Barrière, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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