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:
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
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
Showing 9 citing articles:
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
Hu Wen, Hui Deng, Bingyan Li, et al.
Signal Transduction and Targeted Therapy (2025) Vol. 10, Iss. 1
Open Access | Times Cited: 4
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
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
iPSC models of mitochondrial diseases
Sonja Heiduschka, Alessandro Prigione
Neurobiology of Disease (2025), pp. 106822-106822
Open Access
Sonja Heiduschka, Alessandro Prigione
Neurobiology of Disease (2025), pp. 106822-106822
Open Access
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
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
Chao Chen, Min‐Xin Guan
Journal of Biomedical Science (2023) Vol. 30, Iss. 1
Open Access | Times Cited: 9
[Gene therapy strategies and prospects for neurofibromatosis type 1].
Tingting Zheng, Beiyao Zhu, Zhichao Wang, et al.
PubMed (2024) Vol. 38, Iss. 1, pp. 1-8
Closed Access | Times Cited: 1
Tingting Zheng, Beiyao Zhu, Zhichao Wang, et al.
PubMed (2024) Vol. 38, Iss. 1, pp. 1-8
Closed Access | Times Cited: 1
The application of brain organoid for drug discovery in mitochondrial diseases
Kristina Xiao Liang
The International Journal of Biochemistry & Cell Biology (2024) Vol. 170, pp. 106556-106556
Open Access | Times Cited: 1
Kristina Xiao Liang
The International Journal of Biochemistry & Cell Biology (2024) Vol. 170, pp. 106556-106556
Open Access | Times Cited: 1
Mitochondrial tRNAGlu 14693A>G Mutation, an “Enhancer” to the Phenotypic Expression of Leber's Hereditary Optic Neuropathy
Lihao Jin, Dingyi Gan, Wentao He, et al.
Advanced Science (2024)
Open Access
Lihao Jin, Dingyi Gan, Wentao He, et al.
Advanced Science (2024)
Open Access
Leber’s hereditary optic neuropathy: Update on the novel genes and therapeutic options
Jui-Lin Hu, Chih-Chien Hsu, Yu‐Jer Hsiao, et al.
Journal of the Chinese Medical Association (2023)
Open Access | Times Cited: 1
Jui-Lin Hu, Chih-Chien Hsu, Yu‐Jer Hsiao, et al.
Journal of the Chinese Medical Association (2023)
Open Access | Times Cited: 1
