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:
Superoxide dismutase 2 ameliorates mitochondrial dysfunction in skin fibroblasts of Leber’s hereditary optic neuropathy patients
Qingru Zhou, Shun Yao, Mingzhu Yang, et al.
Frontiers in Neuroscience (2022) Vol. 16
Open Access | Times Cited: 6
Qingru Zhou, Shun Yao, Mingzhu Yang, et al.
Frontiers in Neuroscience (2022) Vol. 16
Open Access | Times Cited: 6
Showing 6 citing articles:
Atypical Leber Hereditary Optic Neuropathy (LHON) Associated with a Novel MT-CYB:m.15309T>C(Ile188Thr) Variant
Sanja Petrović Pajić, Ana Fakin, Martina Jarc Vidmar, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 108-108
Open Access
Sanja Petrović Pajić, Ana Fakin, Martina Jarc Vidmar, et al.
Genes (2025) Vol. 16, Iss. 1, pp. 108-108
Open Access
Galactose-Replacement Unmasks the Biochemical Consequences of the G11778A Mitochondrial DNA Mutation of LHON in Patient-Derived Fibroblasts
Bryce A. Pasqualotto, Carina Tegeman, Ariel K. Frame, et al.
Experimental Cell Research (2024) Vol. 439, Iss. 1, pp. 114075-114075
Open Access | Times Cited: 1
Bryce A. Pasqualotto, Carina Tegeman, Ariel K. Frame, et al.
Experimental Cell Research (2024) Vol. 439, Iss. 1, pp. 114075-114075
Open Access | Times Cited: 1
Compartmental Differences in the Retinal Ganglion Cell Mitochondrial Proteome
Liam S. C. Lewis, Nikolai P. Skiba, Ying Hao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Liam S. C. Lewis, Nikolai P. Skiba, Ying Hao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy
Tianjiao Zhen, Ya Li, Qingge Guo, et al.
Translational Vision Science & Technology (2023) Vol. 12, Iss. 10, pp. 1-1
Open Access | Times Cited: 1
Tianjiao Zhen, Ya Li, Qingge Guo, et al.
Translational Vision Science & Technology (2023) Vol. 12, Iss. 10, pp. 1-1
Open Access | Times Cited: 1
Preservation of Mitochondrial Function by SkQ1 in Skin Fibroblasts Derived from Patients with Leber’s Hereditary Optic Neuropathy Is Associated with the PINK1/PRKN-Mediated Mitophagy
Jin Xu, Yan Li, Shun Yao, et al.
Biomedicines (2024) Vol. 12, Iss. 9, pp. 2020-2020
Open Access
Jin Xu, Yan Li, Shun Yao, et al.
Biomedicines (2024) Vol. 12, Iss. 9, pp. 2020-2020
Open Access
Case Report: Abnormalities of sperm motility and morphology in a patient with Leber hereditary optic neuropathy: Improvement after idebenone therapy
Christophe Orssaud, Virginie Barraud Lange, Jean Philippe Wolf, et al.
Frontiers in Neurology (2023) Vol. 13
Open Access
Christophe Orssaud, Virginie Barraud Lange, Jean Philippe Wolf, et al.
Frontiers in Neurology (2023) Vol. 13
Open Access
