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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:

Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations
Xavier Suárez‐Calvet, Esther Fernández‐Simón, Daniel Natera‐de Benito, et al.
Cell Death and Disease (2023) Vol. 14, Iss. 9
Open Access | Times Cited: 15

Showing 15 citing articles:

HDAC inhibitors as pharmacological treatment for Duchenne muscular dystrophy: a discovery journey from bench to patients
Chiara Mozzetta, Vittorio Sartorelli, Prem Puri
Trends in Molecular Medicine (2024) Vol. 30, Iss. 3, pp. 278-294
Closed Access | Times Cited: 16
Exploring the therapeutic potential of fibroadipogenic progenitors in muscle disease
Marshall W. Hogarth, Medha P Kurukunda, Karim Ismat, et al.
Journal of Neuromuscular Diseases (2025) Vol. 12, Iss. 1
Closed Access | Times Cited: 1
Profound cellular defects attribute to muscular pathogenesis in the rhesus monkey model of Duchenne muscular dystrophy
Shuaiwei Ren, Xin Fu, Wenting Guo, et al.
Cell (2024)
Closed Access | Times Cited: 7
Label-free proteomic analysis of Duchenne and Becker muscular dystrophy showed decreased sarcomere proteins and increased ubiquitination-related proteins
João Silva, María Xesús Nogueira Pereira, Yara Martins da Silva, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Inhibiting EZH2 complements steroid effects in Duchenne muscular dystrophy
Eun Young Jeon, Yejin Kwak, Hyeji Kang, et al.
Science Advances (2025) Vol. 11, Iss. 11
Open Access
Label-free Detection of Urine Extracellular Vesicles from Duchenne Muscular Dystrophy Patients Using Surface-Enhanced Raman Spectroscopy Combined with Machine Learning Models
Archana Rajavel, Jayasree Kumar, E. S. Narayanan, et al.
ACS Omega (2025)
Open Access
Strategy for drug repurposing in fibroadipogenic replacement during muscle wasting: application to duchenne muscular dystrophy
Izzy Matthews, Priyanka Mehra, Xavier Suárez‐Calvet, et al.
Frontiers in Cell and Developmental Biology (2025) Vol. 13
Open Access
Fibroblast diversification is an embryonic process dependent on muscle contraction
Lavi Coren, Shelly Zaffryar‐Eilot, Anas Odeh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophy
Esther Fernández‐Simón, Patricia Piñol‐Jurado, Rasya Gokul-Nath, et al.
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 1
Moderate-term dimethyl fumarate treatment reduces pathology of dystrophic skeletal and cardiac muscle in a mouse model
Stephanie Kourakis, Cara A. Timpani, Ryan M. Bagaric, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 1
Fibro-adipogenic progenitor cells in skeletal muscle unloading: metabolic and functional impairments
Margarita Sorokina, Danila Bobkov, Н. В. Хромова, et al.
Skeletal Muscle (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Decoding the muscle transcriptome of patients with late-onset Pompe disease reveals markers of disease progression
Alexandra Monceau, Rasya Gokul Nath, Xavier Suárez‐Calvet, et al.
Brain (2024) Vol. 147, Iss. 12, pp. 4213-4226
Open Access
Single‐Nucleus RNA Sequencing Unravels Early Mechanisms of Human Becker Muscular Dystrophy
Zhihao Xie, Chang Liu, Chengyue Sun, et al.
Annals of Neurology (2024) Vol. 96, Iss. 6, pp. 1070-1085
Closed Access
Uncovering the Embryonic Origins of Duchenne Muscular Dystrophy
Philip Barrett, Ke’ale Louie, Jean‐Baptiste Dupont, et al.
WIREs Mechanisms of Disease (2024)
Closed Access
Fibroblast diversification is an embryonic process dependent on muscle contraction
Lavi Coren, Shelly Zaffryar‐Eilot, Anas Odeh, et al.
Cell Reports (2024) Vol. 43, Iss. 12, pp. 115034-115034
Open Access
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