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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:

The Good and the Bad of Mitochondrial Breakups
Hans‐Georg Sprenger, Thomas Langer
Trends in Cell Biology (2019) Vol. 29, Iss. 11, pp. 888-900
Closed Access | Times Cited: 165

Showing 1-25 of 165 citing articles:

Mitochondrial quality control mechanisms as molecular targets in cardiac ischemia–reperfusion injury
Jin Wang, Hao Zhou
Acta Pharmaceutica Sinica B (2020) Vol. 10, Iss. 10, pp. 1866-1879
Open Access | Times Cited: 259
Mitochondrial Fusion: The Machineries In and Out
Song Gao, Junjie Hu
Trends in Cell Biology (2020) Vol. 31, Iss. 1, pp. 62-74
Open Access | Times Cited: 257
Determinants and outcomes of mitochondrial dynamics
Rubén Quintana–Cabrera, Luca Scorrano
Molecular Cell (2023) Vol. 83, Iss. 6, pp. 857-876
Open Access | Times Cited: 150
Dynamic O-GlcNAcylation coordinates ferritinophagy and mitophagy to activate ferroptosis
Fan Yu, Qianping Zhang, Hanyu Liu, et al.
Cell Discovery (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 145
Mitochondrial arginase-2 is essential for IL-10 metabolic reprogramming of inflammatory macrophages
Jennifer K. Dowling, Remsha Afzal, Linden J. Gearing, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 123
Adhesion-mediated mechanosignaling forces mitohormesis
Kevin M. Tharp, Ryo Higuchi‐Sanabria, Greg A. Timblin, et al.
Cell Metabolism (2021) Vol. 33, Iss. 7, pp. 1322-1341.e13
Open Access | Times Cited: 105
Mitochondrial morphology controls fatty acid utilization by changing CPT1 sensitivity to malonyl‐CoA
Jennifer Ngo, Dong Wook Choi, Illana A. Stanley, et al.
The EMBO Journal (2023) Vol. 42, Iss. 11
Open Access | Times Cited: 92
Morphological diversification and functional maturation of human astrocytes in glia-enriched cortical organoid transplanted in mouse brain
Meiyan Wang, Lei Zhang, Sammy Weiser Novak, et al.
Nature Biotechnology (2024)
Closed Access | Times Cited: 30
Rnd3 protects against doxorubicin-induced cardiotoxicity through inhibition of PANoptosis in a Rock1/Drp1/mitochondrial fission-dependent manner
Ge Wen, Xiaohua Zhang, Jie Lin, et al.
Cell Death and Disease (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Pathological Roles of Mitochondrial Oxidative Stress and Mitochondrial Dynamics in Cardiac Microvascular Ischemia/Reperfusion Injury
Hao Zhou, Sam Toan
Biomolecules (2020) Vol. 10, Iss. 1, pp. 85-85
Open Access | Times Cited: 103
Mitophagy protects β cells from inflammatory damage in diabetes
Vaibhav Sidarala, Gemma L. Pearson, Vishal S. Parekh, et al.
JCI Insight (2020) Vol. 5, Iss. 24
Open Access | Times Cited: 99
Metformin alleviates lead-induced mitochondrial fragmentation via AMPK/Nrf2 activation in SH-SY5Y cells
Luoyao Yang, Xiaoyi Li, Anli Jiang, et al.
Redox Biology (2020) Vol. 36, pp. 101626-101626
Open Access | Times Cited: 84
The IGF/Insulin-IGFBP Axis in Corneal Development, Wound Healing, and Disease
Whitney L. Stuard, Rossella Titone, Danielle M. Robertson
Frontiers in Endocrinology (2020) Vol. 11
Open Access | Times Cited: 80
Aberrant mitochondrial morphology and function associated with impaired mitophagy and DNM1L-MAPK/ERK signaling are found in aged mutant Parkinsonian LRRK2R1441Gmice
Huifang Liu, Philip Wing‐Lok Ho, Chi-Ting Leung, et al.
Autophagy (2020) Vol. 17, Iss. 10, pp. 3196-3220
Open Access | Times Cited: 76
Physical Exercise: A Novel Tool to Protect Mitochondrial Health
Daniela Sorriento, Eugenio Di Vaia, Guido Iaccarino
Frontiers in Physiology (2021) Vol. 12
Open Access | Times Cited: 76
The Mitochondrial Permeability Transition: Nexus of Aging, Disease and Longevity
Hagai Rottenberg, Jan B. Hoek
Cells (2021) Vol. 10, Iss. 1, pp. 79-79
Open Access | Times Cited: 64
Mitochondrial Dynamics: A Potential Therapeutic Target for Ischemic Stroke
Xiangyue Zhou, Han‐Min Chen, Ling Wang, et al.
Frontiers in Aging Neuroscience (2021) Vol. 13
Open Access | Times Cited: 59
Oxalate-induced apoptosis through ERS-ROS–NF-κB signalling pathway in renal tubular epithelial cell
Shaoxiong Ming, Jia Tian, Ke Ma, et al.
Molecular Medicine (2022) Vol. 28, Iss. 1
Open Access | Times Cited: 50
Nutrient-sensing mTORC1 and AMPK pathways in chronic kidney diseases
Christopher Huynh, Jaewhee Ryu, Jooho Lee, et al.
Nature Reviews Nephrology (2022) Vol. 19, Iss. 2, pp. 102-122
Closed Access | Times Cited: 49
PINK1/TAX1BP1-directed mitophagy attenuates vascular endothelial injury induced by copper oxide nanoparticles
Yinzhen Fan, Zhenli Cheng, Lejiao Mao, et al.
Journal of Nanobiotechnology (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 43
Light-activated mitochondrial fission through optogenetic control of mitochondria-lysosome contacts
Kangqiang Qiu, Weiwei Zou, Hongbao Fang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 42
AMPK is a mechano-metabolic sensor linking cell adhesion and mitochondrial dynamics to Myosin-dependent cell migration
Eva Crosas‐Molist, Vittoria Graziani, Óscar Maiques, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 40
mcPGK1-dependent mitochondrial import of PGK1 promotes metabolic reprogramming and self-renewal of liver TICs
Zhenzhen Chen, Qiankun He, Tiankun Lu, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 34
Small molecule agonist of mitochondrial fusion repairs mitochondrial dysfunction
Yingjie Guo, Huan Zhang, Chen Yan, et al.
Nature Chemical Biology (2023) Vol. 19, Iss. 4, pp. 468-477
Closed Access | Times Cited: 33
Role of Mitochondrial Dynamics in Heart Diseases
Takeshi Tokuyama, Shigeru Yanagi
Genes (2023) Vol. 14, Iss. 10, pp. 1876-1876
Open Access | Times Cited: 25
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