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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:

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

Showing 11 citing articles:

Molecular mechanisms of aging and anti-aging strategies
Yumeng Li, Xutong Tian, Juyue Luo, et al.
Cell Communication and Signaling (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 61
AMPK as a mediator of tissue preservation: time for a shift in dogma?
Henning T. Langer, Maria Rohm, Marcus D. Goncalves, et al.
Nature Reviews Endocrinology (2024) Vol. 20, Iss. 9, pp. 526-540
Closed Access | Times Cited: 12
Tetramethylpyrazine Nitrone alleviates D-galactose-induced murine skeletal muscle aging and motor deficits by activating the AMPK signaling pathway
Lulin Nie, Kaiwu He, Chaoming Qiu, et al.
Biomedicine & Pharmacotherapy (2024) Vol. 173, pp. 116415-116415
Open Access | Times Cited: 5
Ferulic acid restores mitochondrial dynamics and autophagy via AMPK signaling pathway in a palmitate-induced hepatocyte model of metabolic syndrome
Yitong Li, Weiyang Zhao, Ali Tahir Sair, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Clinical Approaches for Mitochondrial Diseases
Seongho Hong, Sanghun Kim, Kyoungmi Kim, et al.
Cells (2023) Vol. 12, Iss. 20, pp. 2494-2494
Open Access | Times Cited: 10
Skeletal Muscle Mitochondrial and Autophagic Dysregulation Are Modifiable in Spinal Muscular Atrophy
Andrew I. Mikhail, Sean Y. Ng, Donald Xhuti, et al.
Journal of Cachexia Sarcopenia and Muscle (2025) Vol. 16, 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
Perspectives on the interpretation of mitochondrial responses during skeletal muscle disuse‐induced atrophy
Luca J. Delfinis, Shahrzad Khajehzadehshoushtar, Christopher G. R. Perry
The Journal of Physiology (2025)
Open Access
Mitochondrial dynamics and the significance of its disturbances in the development of childhood diseases. Part I. Physiological and neurological aspects
В. С. Сухоруков, Т. И. Баранич, А. В. Егорова, et al.
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2024) Vol. 69, Iss. 1, pp. 25-33
Open Access | Times Cited: 1
Targeting mitochondrial Ca2+ uptake for the treatment of amyotrophic lateral sclerosis
Renjia Zhong, Michael T. Rua, Lan Wei‐LaPierre
The Journal of Physiology (2023) Vol. 602, Iss. 8, pp. 1519-1549
Closed Access | Times Cited: 3
Cytokine-Supplemented Maturation Medium Enhances Cytoplasmic and Nuclear Maturation in Bovine Oocytes
R. Blocher, Ying Liu, Tayler Patrick, et al.
Animals (2024) Vol. 14, Iss. 12, pp. 1837-1837
Open Access
Exhaustion, rather than lack of infiltration and persistence, of CAR-T cells hampers the efficacy of CAR-T therapy in an orthotopic PDAC xenograft model
Yuta Takeuchi, Yizheng Wang, Katsunori Sasaki, et al.
Biomedicine & Pharmacotherapy (2023) Vol. 170, pp. 116052-116052
Open Access | Times Cited: 1
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