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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:

Epigenetic modifications in muscle regeneration and progression of Duchenne muscular dystrophy
Anna Rugowska, Alicja Starosta, Patryk Konieczny
Clinical Epigenetics (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Histone deacetylase inhibition with givinostat: a multi-targeted mode of action with the potential to halt the pathological cascade of Duchenne muscular dystrophy
Annemieke Aartsma‐Rus
Frontiers in Cell and Developmental Biology (2025) Vol. 12
Open Access | Times Cited: 1
Oestrogen suppresses the adipogenesis of fibro/adipogenic progenitors through reactivating the METTL3–ESR1‐mediated loop in post‐menopausal females
Hao Zhou, Shujing Feng, Jinkui Cai, et al.
Clinical and Translational Medicine (2025) Vol. 15, Iss. 2
Open Access | Times Cited: 1
Long noncoding RNAlncMREFpromotes myogenic differentiation and muscle regeneration by interacting with the Smarca5/p300 complex
Wei Lv, Wei Jiang, Hongmei Luo, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 18, pp. 10733-10755
Open Access | Times Cited: 32
Extraocular muscle stem cells exhibit distinct cellular properties associated with non-muscle molecular signatures
Daniela Di Girolamo, Maria Benavente-Diaz, Melania Murolo, et al.
Development (2024) Vol. 151, Iss. 4
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
Disturbance of calcium homeostasis and myogenesis caused by TET2 deletion in muscle stem cells
Haoyuan Zhang, Sheng Wang, Qiangwei Zhou, et al.
Cell Death Discovery (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 16
Determinants of epigenetic resistance to HDAC inhibitors in dystrophic fibro‐adipogenic progenitors
Silvia Consalvi, Luca Tucciarone, Elisa Macrì, et al.
EMBO Reports (2022) Vol. 23, Iss. 6
Open Access | Times Cited: 15
Dystrophin- and Utrophin-Based Therapeutic Approaches for Treatment of Duchenne Muscular Dystrophy: A Comparative Review
Sylwia Szwec, Zuzanna Kapłucha, Jeffrey S. Chamberlain, et al.
BioDrugs (2023) Vol. 38, Iss. 1, pp. 95-119
Open Access | Times Cited: 9
Arabidopsis thaliana: a powerful model organism to explore histone modifications and their upstream regulations
Yu Yang, Sihan Wang, Ziqin Wang, et al.
Epigenetics (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 7
Rho/SRF Inhibitor Modulates Mitochondrial Functions
Pankaj Patyal, Bachkhoa Nguyen, Xiaomin Zhang, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 19, pp. 11536-11536
Open Access | Times Cited: 12
Signaling pathways and regulatory networks in quail skeletal muscle development: insights from whole transcriptome sequencing
Wentao Zhang, Jing Liu, Yanan Zhou, et al.
Poultry Science (2024) Vol. 103, Iss. 5, pp. 103603-103603
Open Access | Times Cited: 2
An Emerging Role for Epigenetics in Cerebral Palsy
Brigette Romero, Karyn G. Robinson, Mona Batish, et al.
Journal of Personalized Medicine (2021) Vol. 11, Iss. 11, pp. 1187-1187
Open Access | Times Cited: 15
Cellular pathogenesis of Duchenne muscular dystrophy: progressive myofibre degeneration, chronic inflammation, reactive myofibrosis and satellite cell dysfunction
Paul Dowling, Dieter Swandulla, Kay Ohlendieck
European Journal of Translational Myology (2023)
Open Access | Times Cited: 6
Resolution of fibrosis in mdx dystrophic mouse after oral consumption of N-163 strain of Aureobasidium pullulans produced β-glucan
Senthilkumar Preethy, Yoshitsugu Aoki, Katsura Minegishi, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 4
Epitranscriptomics as a New Layer of Regulation of Gene Expression in Skeletal Muscle: Known Functions and Future Perspectives
Carol Imbriano, Viviana Moresi, Silvia Belluti, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 20, pp. 15161-15161
Open Access | Times Cited: 4
Systemic Treatment of Body‐Wide Duchenne Muscular Dystrophy Symptoms
Patryk Konieczny
Clinical Pharmacology & Therapeutics (2024) Vol. 116, Iss. 6, pp. 1472-1484
Open Access | Times Cited: 1
A Review on Epigenetics of Human Inherited Diseases: Molecular Diagnosis
Bibi Shazia Sabir
International Journal of Innovative Science and Research Technology (IJISRT) (2024), pp. 696-703
Open Access | Times Cited: 1
Aronia-derived anthocyanins and metabolites ameliorate TNFα-induced disruption of myogenic differentiation in satellite cells
Xiaocao Liu, Nina Shangguan, Fulong Zhang, et al.
Biochemical and Biophysical Research Communications (2024) Vol. 733, pp. 150687-150687
Closed Access | Times Cited: 1
Effects of PGC-1α overexpression on the myogenic response during skeletal muscle regeneration
Tyrone A. Washington, Wesley S. Haynie, Eleanor R. Schrems, et al.
Sports Medicine and Health Science (2022) Vol. 4, Iss. 3, pp. 198-208
Open Access | Times Cited: 6
Resolution of fibrosis in mdx dystrophic mouse after oral consumption of N-163 strain ofAureobasidium pullulansproduced biological response modifier β-glucan (BRMG)
Senthilkumar Preethy, Yoshitsugu Aoki, Katsura Minegishi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 6
Post-natal muscle growth and protein turnover: a narrative review of current understanding
D. J. Millward
Nutrition Research Reviews (2023) Vol. 37, Iss. 1, pp. 141-168
Open Access | Times Cited: 3
The discovery of the DNA methylation episignature for Duchenne muscular dystrophy
Leighton Schreyer, Jack Reilly, Haley McConkey, et al.
Neuromuscular Disorders (2022) Vol. 33, Iss. 1, pp. 5-14
Closed Access | Times Cited: 5
Extraocular muscle stem cells exhibit distinct cellular properties associated with non-muscle molecular signatures
Daniela Di Girolamo, Maria Benavente-Diaz, Alexandre Grimaldi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
A Method Using One Fluorophore Signal in Sanger Read to Determine CpG Methylation in Bisulfite Converted DNA
Dmitriy Karpenko
Russian Journal of Genetics (2023) Vol. 59, Iss. 11, pp. 1255-1262
Closed Access | Times Cited: 2
Computational discovery of novel inhibitory candidates targeting versatile transcriptional repressor MBD2
Zihni Onur Çalışkaner
Journal of Molecular Modeling (2022) Vol. 28, Iss. 10
Closed Access | Times Cited: 3
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