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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:

Pathological mitophagy disrupts mitochondrial homeostasis in Leber’s hereditary optic neuropathy
Alberto Danese, Simone Patergnani, Alessandra Maresca, et al.
Cell Reports (2022) Vol. 40, Iss. 3, pp. 111124-111124
Open Access | Times Cited: 47

Showing 1-25 of 47 citing articles:

Mitochondrial dysfunction and skeletal muscle atrophy: Causes, mechanisms, and treatment strategies
Gökhan Burçin Kubat, Esmaa Bouhamida, Öner Ülger, et al.
Mitochondrion (2023) Vol. 72, pp. 33-58
Closed Access | Times Cited: 50
Copper homeostasis and cuproptosis in mitochondria
Ziying Tian, Su Jiang, Jieyu Zhou, et al.
Life Sciences (2023) Vol. 334, pp. 122223-122223
Closed Access | Times Cited: 42
Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial
Patrick Yu‐Wai‐Man, Valério Carelli, Nancy J. Newman, et al.
Cell Reports Medicine (2024) Vol. 5, Iss. 3, pp. 101437-101437
Open Access | Times Cited: 17
Mitochondrial diseases: from molecular mechanisms to therapeutic advances
Hu Wen, Hui Deng, Bingyan Li, et al.
Signal Transduction and Targeted Therapy (2025) Vol. 10, Iss. 1
Open Access | Times Cited: 4
Understanding the molecular basis and pathogenesis of hereditary optic neuropathies: towards improved diagnosis and management
Nancy J. Newman, Patrick Yu‐Wai‐Man, Valérie Biousse, et al.
The Lancet Neurology (2022) Vol. 22, Iss. 2, pp. 172-188
Open Access | Times Cited: 57
The Tricky Connection between Extracellular Vesicles and Mitochondria in Inflammatory-Related Diseases
Tommaso Di Mambro, Giulia Pellielo, Esther Densu Agyapong, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8181-8181
Open Access | Times Cited: 25
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy
Serena J. Aleo, Valentina Del Dotto, Martina Romagnoli, et al.
Cell Reports Medicine (2024) Vol. 5, Iss. 2, pp. 101383-101383
Open Access | Times Cited: 15
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicity
Marzena Kurzawa‐Akanbi, Nikolaos Tzoumas, Julio C. Corral-Serrano, et al.
Progress in Retinal and Eye Research (2024) Vol. 100, pp. 101248-101248
Open Access | Times Cited: 11
Mitochondrial optic neuropathies
Valério Carelli, Chiara La Morgia, Patrick Yu‐Wai‐Man
Handbook of clinical neurology (2023), pp. 23-42
Closed Access | Times Cited: 22
Modeling mitochondrial DNA diseases: from base editing to pluripotent stem‐cell‐derived organoids
Isabella Tolle, Valeria Tiranti, Alessandro Prigione
EMBO Reports (2023) Vol. 24, Iss. 4
Open Access | Times Cited: 19
Autophagy and Senescence: The Molecular Mechanisms and Implications in Liver Diseases
Li Qiao, Yan Lin, Guangyu Liang, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 16880-16880
Open Access | Times Cited: 18
Mitochondrial retinopathies and optic neuropathies: the impact of retinal imaging on modern understanding of pathogenesis, diagnosis, and management
Enrico Borrelli, Francesco Bandello, Camiel J. F. Boon, et al.
Progress in Retinal and Eye Research (2024) Vol. 101, pp. 101264-101264
Closed Access | Times Cited: 6
Deficient tRNA posttranscription modification dysregulated the mitochondrial quality controls and apoptosis
Yunfan He, Zhu Gao, Xincheng Li, et al.
iScience (2024) Vol. 27, Iss. 2, pp. 108883-108883
Open Access | Times Cited: 5
The Complex Relationship between Hypoxia Signaling, Mitochondrial Dysfunction and Inflammation in Calcific Aortic Valve Disease: Insights from the Molecular Mechanisms to Therapeutic Approaches
Esmaa Bouhamida, Giampaolo Morciano, Gaia Pedriali, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 13, pp. 11105-11105
Open Access | Times Cited: 11
A bibliometric analysis of optic atrophy from 2003 to 2023: research trends and hot spots
Liyuan Wang, Tianyang Yu, Runze Wang, et al.
Frontiers in Medicine (2025) Vol. 11
Open Access
iPSC models of mitochondrial diseases
Sonja Heiduschka, Alessandro Prigione
Neurobiology of Disease (2025), pp. 106822-106822
Open Access
Faecalibacterium prausnitzii Suppresses Mitophagy to Alleviate Muscle Atrophy in Chronic Renal Failure With Protein‐Energy Wasting
Jingwen Ni, Yuting Yin, Pan Liang, et al.
Apmis (2025) Vol. 133, Iss. 3
Closed Access
Creation of Mitochondrial Disease Models Using Mitochondrial DNA Editing
Victoria A. Khotina, Andrey Y. Vinokurov, Mariam Bagheri Ekta, et al.
Biomedicines (2023) Vol. 11, Iss. 2, pp. 532-532
Open Access | Times Cited: 10
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
Mitochondria in Retinal Ganglion Cells: Unraveling the Metabolic Nexus and Oxidative Stress
Tsai-Hsuan Yang, Eugene Yu‐Chuan Kang, Pei‐Hsuan Lin, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 8626-8626
Open Access | Times Cited: 3
Idebenone improves mitochondrial respiratory activity and attenuates oxidative damage via the SIRT3-SOD2 pathway in a prion disease cell model
Zhixin Sun, Pei Wen, Dongming Yang, et al.
Life Sciences (2025) Vol. 366-367, pp. 123481-123481
Closed Access
Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber’s hereditary optic neuropathy
Jia‐Rong Chen, Chao Chen, Jie Chen, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 9, pp. 1539-1551
Closed Access | Times Cited: 9
Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation
Jing Wang, Yanchun Ji, Cheng Ai, et al.
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 9
Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations
Chao Chen, Min‐Xin Guan
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 9
Dynamic adaptive hydrogel facilitates neuroregeneration in segmental nerve deficits via immunomodulation and mitochondrial homeostasis
Xiaozhong Yang, Jizhao Dong, Yunfeng Tang, et al.
Chemical Engineering Journal (2024) Vol. 494, pp. 152890-152890
Closed Access | Times Cited: 2
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