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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:

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

Showing 22 citing articles:

Location and interaction of idebenone and mitoquinone in a membrane similar to the inner mitochondrial membrane. Comparison with ubiquinone 10
José Villalaı́n
Free Radical Biology and Medicine (2024) Vol. 222, pp. 211-222
Open Access | Times Cited: 5
Origins of tissue and cell-type specificity in mitochondrial DNA (mtDNA) disease
Stephen P. Burr, Patrick F. Chinnery
Human Molecular Genetics (2024) Vol. 33, Iss. R1, pp. R3-R11
Open Access | Times Cited: 4
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
SIRT1-based therapy targets a gene program involved in mitochondrial turnover in a model of retinal neurodegeneration
Brahim Chaqour, Jon Rossman, Miranda Meng, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Toxic ethambuthol-induced optic neuropathy in a patient with OPA1 mutation
Claire Meyniel, Patrizia Amati‐Bonneau, Pascal Reynier, et al.
Canadian Journal of Ophthalmology (2025)
Closed Access
Inhibition of cGMP‐Signalling Rescues Retinal Ganglion Cells From Axotomy‐Induced Degeneration
Katia Ihadadene, Azdah Hamed A Fallatah, Yu Zhu, et al.
Journal of Neurochemistry (2025) Vol. 169, Iss. 4
Open Access
Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree
Sonia Emperador, Mouna Habbane, Ester López‐Gallardo, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 3
Alterations in ganglion cell and nerve fiber layer in Leber hereditary optic neuropathy across clinical stages
Michael Oeverhaus, Mareile Knetsch, Ying Chen, et al.
BMC Ophthalmology (2025) Vol. 25, Iss. 1
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
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
Optic neuropathy in methylmalonic acidemia: the role of neuroprotection
Sergio Pinar‐Sueiro, Ricardo Martínez‐Fernández, Sergio Lage, et al.
Journal of Inherited Metabolic Disease (2010) Vol. 33, Iss. S3, pp. 199-203
Closed Access | Times Cited: 35
Anti-inflammatory reprogramming of microglia cells by metabolic modulators to counteract neurodegeneration; a new role for Ranolazine
Ilaria Piano, Arianna Votta, Patrizia Colucci, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 6
Ethambutol-induced optic neuropathy: Functional and structural changes in the retina and optic nerve
Sagnik Sen, Sohini Mandal, Mousumi Banerjee, et al.
Seminars in Ophthalmology (2022) Vol. 37, Iss. 6, pp. 730-739
Closed Access | Times Cited: 8
Relapsing White Matter Disease and Subclinical Optic Neuropathy
Kimberly A. O'Neill, Andrew Dugue, Nicolas J. Abreu, et al.
Neurology Neuroimmunology & Neuroinflammation (2024) Vol. 11, Iss. 2
Open Access | Times Cited: 1
Hereditary Optic Neuropathies: An Updated Review
Samuel Lee, Caroline Mura, Nicolas J. Abreu, et al.
Journal of Clinical & Translational Ophthalmology (2024) Vol. 2, Iss. 3, pp. 64-78
Open Access | Times Cited: 1
Defective post-transcriptional modification of tRNA disrupts mitochondrial homeostasis in Leber’s hereditary optic neuropathy
Juanjuan Zhang, Wenxu Li, Zhen Liu, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 9, pp. 107728-107728
Open Access | Times Cited: 1
Meta-analysis of treatment outcomes for patients with m.11778G>A MT-ND4 Leber Hereditary Optic Neuropathy
Nancy J. Newman, Valérie Biousse, Patrick Yu‐Wai‐Man, et al.
Survey of Ophthalmology (2024) Vol. 70, Iss. 2, pp. 283-295
Open Access | Times Cited: 1
Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells
Miguel Ladero, J.A. Reche-Sainz, M. Esther Gallardo
Bioengineering (2024) Vol. 11, Iss. 1, pp. 52-52
Open Access | Times Cited: 1
Insights on the Genetic and Phenotypic Complexities of Optic Neuropathies
Fabiana D’Esposito, Marco Zeppieri, M. Francesca Cordeiro, et al.
Genes (2024) Vol. 15, Iss. 12, pp. 1559-1559
Open Access | Times Cited: 1
Assessment of objective visual function following idebenone administration in patients with leber hereditary optic neuropathy
Yoichiro Masuda, Hiroto Ishikawa, Hitoshi Ishikawa, et al.
Japanese Journal of Ophthalmology (2024) Vol. 68, Iss. 5, pp. 548-555
Closed Access
RTN4IP1 is essential for the final stages of mitochondrial complex I assembly and coenzyme Q biosynthesis
Monika Oláhová, Rachel M. Guerra, Jack J. Collier, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Mitochondrial disorders due to mutations in the nuclear genome
Patrick F. Chinnery, Rita Horváth
Elsevier eBooks (2024), pp. 521-532
Closed Access
High frequency of mitochondrial DNA rearrangements in the peripheral blood of adults with intellectual disability
Bengisu Kevser Bulduk, J. Valero, Leire Torres-Egurrola, et al.
Journal of Intellectual Disability Research (2024)
Closed Access
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