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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.

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Showing 1-25 of 86 citing articles:

Mitophagy in cardiovascular diseases: molecular mechanisms, pathogenesis, and treatment
Amir Ajoolabady, Mario Chiong, Sergio Lavandero, et al.
Trends in Molecular Medicine (2022) Vol. 28, Iss. 10, pp. 836-849
Open Access | Times Cited: 119
FNDC5/Irisin: Physiology and Pathophysiology
Rashid Waseem, Anas Shamsi, Taj Mohammad, et al.
Molecules (2022) Vol. 27, Iss. 3, pp. 1118-1118
Open Access | Times Cited: 105
Irisin protects against vascular calcification by activating autophagy and inhibiting NLRP3-mediated vascular smooth muscle cell pyroptosis in chronic kidney disease
Qi Pang, Peiwen Wang, Yajing Pan, et al.
Cell Death and Disease (2022) Vol. 13, Iss. 3
Open Access | Times Cited: 79
Regulation of autophagy of the heart in ischemia and reperfusion
С. В. Попов, А. V. Mukhomedzyanov, Nikita S. Voronkov, et al.
APOPTOSIS (2022) Vol. 28, Iss. 1-2, pp. 55-80
Closed Access | Times Cited: 75
Mitochondrial quality control in human health and disease
Bohao Liu, Chen-Zhen Xu, Yi Liu, et al.
Military Medical Research (2024) Vol. 11, Iss. 1
Open Access | Times Cited: 29
Traditional Chinese medicine and mitophagy: A novel approach for cardiovascular disease management
Jinhui Wang, Junbo Zou, Yajun Shi, et al.
Phytomedicine (2024) Vol. 128, pp. 155472-155472
Closed Access | Times Cited: 20
Mitochondrial quality surveillance as a therapeutic target in myocardial infarction
Hang Zhu, Sam Toan, David Mui, et al.
Acta Physiologica (2020) Vol. 231, Iss. 3
Closed Access | Times Cited: 124
FNDC5/Irisin System in Neuroinflammation and Neurodegenerative Diseases: Update and Novel Perspective
Patrizia Pignataro, Manuela Dicarlo, Roberta Zerlotin, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 4, pp. 1605-1605
Open Access | Times Cited: 92
Biological Aspects of Selected Myokines in Skeletal Muscle: Focus on Aging
Rosa Mancinelli, F Checcaglini, Francesco Coscia, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8520-8520
Open Access | Times Cited: 75
Mitochondrial Dynamics, Mitophagy, and Mitochondria–Endoplasmic Reticulum Contact Sites Crosstalk Under Hypoxia
Shuying Wang, Jin Tan, Yuyang Miao, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 58
Irisin, a fascinating field in our times
Jing‐Fu Bao, Qin-Ying She, Panpan Hu, et al.
Trends in Endocrinology and Metabolism (2022) Vol. 33, Iss. 9, pp. 601-613
Closed Access | Times Cited: 55
Irisin, an exercise-induced bioactive peptide beneficial for health promotion during aging process
Hu Zhang, Xiaowen Wu, Jiling Liang, et al.
Ageing Research Reviews (2022) Vol. 80, pp. 101680-101680
Closed Access | Times Cited: 54
Mitochondrial dynamics proteins as emerging drug targets
Emmanouil Zacharioudakis, Evripidis Gavathiotis
Trends in Pharmacological Sciences (2022) Vol. 44, Iss. 2, pp. 112-127
Open Access | Times Cited: 47
Irisin Promotes Cardiac Homing of Intravenously Delivered MSCs and Protects against Ischemic Heart Injury
Wenjun Yan, Youhu Chen, Yongzhen Guo, et al.
Advanced Science (2022) Vol. 9, Iss. 7
Open Access | Times Cited: 38
Role of Mitochondrial Dynamics in Heart Diseases
Takeshi Tokuyama, Shigeru Yanagi
Genes (2023) Vol. 14, Iss. 10, pp. 1876-1876
Open Access | Times Cited: 23
The Role of FNDC5/Irisin in Cardiovascular Disease
Maciej Grzeszczuk, Piotr Dzięgiel, Katarzyna Nowińska
Cells (2024) Vol. 13, Iss. 3, pp. 277-277
Open Access | Times Cited: 11
Irisin: A New Code Uncover the Relationship of Skeletal Muscle and Cardiovascular Health During Exercise
Chunlian Ma, Haichao Ding, Yuting Deng, et al.
Frontiers in Physiology (2021) Vol. 12
Open Access | Times Cited: 53
FUNDC1: A Promising Mitophagy Regulator at the Mitochondria-Associated Membrane for Cardiovascular Diseases
Guoyong Li, Junli Li, Ruochen Shao, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 52
The Emerging Role of Irisin in Cardiovascular Diseases
Jinjuan Fu, Fangtang Li, Yuanjuan Tang, et al.
Journal of the American Heart Association (2021) Vol. 10, Iss. 20
Open Access | Times Cited: 44
Mitophagy Regulation Following Myocardial Infarction
Annie Turkieh, Yara El Masri, F Pinet, et al.
Cells (2022) Vol. 11, Iss. 2, pp. 199-199
Open Access | Times Cited: 37
Irisin protects against doxorubicin-induced cardiotoxicity by improving AMPK-Nrf2 dependent mitochondrial fusion and strengthening endogenous anti-oxidant defense mechanisms
Caili Zhuo, Juan-Juan Xin, Wenjing Huang, et al.
Toxicology (2023) Vol. 494, pp. 153597-153597
Closed Access | Times Cited: 19
The “irisin system”: From biological roles to pharmacological and nutraceutical perspectives
Lorenzo Flori, Lara Testai, Vincenzo Calderone
Life Sciences (2020) Vol. 267, pp. 118954-118954
Closed Access | Times Cited: 46
Irisin and Autophagy: First Update
Mirko Pesce, Patrizia Ballerini, Teresa Paolucci, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 20, pp. 7587-7587
Open Access | Times Cited: 41
RETRACTED: Oxidized LDL Causes Endothelial Apoptosis by Inhibiting Mitochondrial Fusion and Mitochondria Autophagy
Jia Zheng, Chengzhi Lu
Frontiers in Cell and Developmental Biology (2020) Vol. 8
Open Access | Times Cited: 40
Exercise Training Enhances Myocardial Mitophagy and Improves Cardiac Function via Irisin/FNDC5-PINK1/Parkin Pathway in MI Mice
Hangzhuo Li, Shuguang Qin, Qiaoqin Liang, et al.
Biomedicines (2021) Vol. 9, Iss. 6, pp. 701-701
Open Access | Times Cited: 37
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