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:
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
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
Showing 26-50 of 57 citing articles:
Safety of Lenadogene Nolparvovec Gene Therapy Over 5 Years in 189 Patients With Leber Hereditary Optic Neuropathy
Catherine Vignal, Patrick Yu‐Wai‐Man, Nancy J. Newman, et al.
American Journal of Ophthalmology (2022) Vol. 249, pp. 108-125
Open Access | Times Cited: 15
Catherine Vignal, Patrick Yu‐Wai‐Man, Nancy J. Newman, et al.
American Journal of Ophthalmology (2022) Vol. 249, pp. 108-125
Open Access | Times Cited: 15
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
RecessiveMECRpathogenic variants cause an LHON-like optic neuropathy
Claudio Fiorini, Andrea Degiorgi, Maria Lucia Cascavilla, et al.
Journal of Medical Genetics (2023) Vol. 61, Iss. 1, pp. 93-101
Open Access | Times Cited: 9
Claudio Fiorini, Andrea Degiorgi, Maria Lucia Cascavilla, et al.
Journal of Medical Genetics (2023) Vol. 61, Iss. 1, pp. 93-101
Open Access | Times Cited: 9
OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets
David Wong, Joshua Harvey, Neringa Jurkutė, et al.
Journal of Neuro-Ophthalmology (2023)
Open Access | Times Cited: 8
David Wong, Joshua Harvey, Neringa Jurkutė, et al.
Journal of Neuro-Ophthalmology (2023)
Open Access | Times Cited: 8
Preparation of Viable Human Neurites for Neurobiological and Neurodegeneration Studies
Markus Brüll, Nils Geese, Ivana Celardo, et al.
Cells (2024) Vol. 13, Iss. 3, pp. 242-242
Open Access | Times Cited: 3
Markus Brüll, Nils Geese, Ivana Celardo, et al.
Cells (2024) Vol. 13, Iss. 3, pp. 242-242
Open Access | Times Cited: 3
AFG3L2 and ACO2-Linked Dominant Optic Atrophy: Genotype–Phenotype Characterization Compared to OPA1 Patients
Giulia Amore, Martina Romagnoli, Michele Carbonelli, et al.
American Journal of Ophthalmology (2024) Vol. 262, pp. 114-124
Closed Access | Times Cited: 2
Giulia Amore, Martina Romagnoli, Michele Carbonelli, et al.
American Journal of Ophthalmology (2024) Vol. 262, pp. 114-124
Closed Access | Times Cited: 2
Evaluating the efficacy of vatiquinone in preclinical models of mitochondrial disease
Ernst‐Bernhard Kayser, Yihan Chen, Michael Mulholland, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 2
Ernst‐Bernhard Kayser, Yihan Chen, Michael Mulholland, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 2
Uncovering the Genetics and Physiology behind Optic Neuritis
Ilaria Del Negro, Giada Pauletto, Lorenzo Verriello, et al.
Genes (2023) Vol. 14, Iss. 12, pp. 2192-2192
Open Access | Times Cited: 5
Ilaria Del Negro, Giada Pauletto, Lorenzo Verriello, et al.
Genes (2023) Vol. 14, Iss. 12, pp. 2192-2192
Open Access | Times Cited: 5
Mitochondrial encephalomyopathy
Yi Shiau Ng, Robert McFarland
Handbook of clinical neurology (2023), pp. 563-585
Closed Access | Times Cited: 4
Yi Shiau Ng, Robert McFarland
Handbook of clinical neurology (2023), pp. 563-585
Closed Access | Times Cited: 4
Neuroimaging changes in the pregeniculate visual pathway and chiasmal enlargement in Leber hereditary optic neuropathy
Xintong Xu, Huanfen Zhou, Mingming Sun, et al.
British Journal of Ophthalmology (2024) Vol. 108, Iss. 9, pp. 1313-1317
Open Access | Times Cited: 1
Xintong Xu, Huanfen Zhou, Mingming Sun, et al.
British Journal of Ophthalmology (2024) Vol. 108, Iss. 9, pp. 1313-1317
Open Access | Times Cited: 1
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
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
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
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
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
Miguel Ladero, J.A. Reche-Sainz, M. Esther Gallardo
Bioengineering (2024) Vol. 11, Iss. 1, pp. 52-52
Open Access | Times Cited: 1
Progress in diagnosis and treatment of Leber’s hereditary optic neuropathy
Qingyue Ma, Ying Sun, Ke Lei, et al.
Journal of Molecular Medicine (2023)
Closed Access | Times Cited: 2
Qingyue Ma, Ying Sun, Ke Lei, et al.
Journal of Molecular Medicine (2023)
Closed Access | Times Cited: 2
Bilateral optic atrophy in Wilson disease: A case report and literature review
Fei Chen, Chunli Chen, Yang Zhang, et al.
Clinics and Research in Hepatology and Gastroenterology (2024) Vol. 48, Iss. 3, pp. 102299-102299
Closed Access
Fei Chen, Chunli Chen, Yang Zhang, et al.
Clinics and Research in Hepatology and Gastroenterology (2024) Vol. 48, Iss. 3, pp. 102299-102299
Closed Access
Molecular basis of hereditary cardiomyopathy: A systematic review
Amar Silajdžić, Urtina Malja, Erisa Malja, et al.
World Journal of Biology Pharmacy and Health Sciences (2024) Vol. 18, Iss. 2, pp. 220-226
Open Access
Amar Silajdžić, Urtina Malja, Erisa Malja, et al.
World Journal of Biology Pharmacy and Health Sciences (2024) Vol. 18, Iss. 2, pp. 220-226
Open Access
Clinical Visual Electrophysiology: A Tool for Studying Inherited Retinal Disorders
J. Vernon Odom, Monique Leys
Essentials in ophthalmology/Essentials ophthalmology (2024), pp. 1-34
Closed Access
J. Vernon Odom, Monique Leys
Essentials in ophthalmology/Essentials ophthalmology (2024), pp. 1-34
Closed Access
A case for the use of chemotherapy in hereditary mitochondrial optic neuropathies: Successful administration of cisplatin/etoposide in a male patient with testicular seminoma and Leber's hereditary optic neuropathy
Jean-Luc Vrisakis, Clare L. Fraser, Adel Shahnam, et al.
Clinical Case Reports (2024) Vol. 12, Iss. 7
Open Access
Jean-Luc Vrisakis, Clare L. Fraser, Adel Shahnam, et al.
Clinical Case Reports (2024) Vol. 12, Iss. 7
Open Access
The Morphology of Normal, Aging, and Glaucomatous Optic Nerves
Tatjana Jakobs
Elsevier eBooks (2024)
Closed Access
Tatjana Jakobs
Elsevier eBooks (2024)
Closed Access
Nerfs crâniens — Olfaction (I) ; vision : nerf optique (II) et nerfs oculomoteurs (III, IV et VI) ; audition et équilibre (VIII)
J Cambier, M Masson, Catherine Masson-Boivin, et al.
Elsevier eBooks (2024), pp. 71-98
Closed Access
J Cambier, M Masson, Catherine Masson-Boivin, et al.
Elsevier eBooks (2024), pp. 71-98
Closed Access
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes
Yuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
Brain (2024)
Open Access
Yuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
Brain (2024)
Open Access
Disruption of mitochondrial homeostasis and permeability transition pore opening in OPA1 iPSC-derived retinal ganglion cells
M. A. Whitehead, Joshua Harvey, Paul E. Sladen, et al.
Research Square (Research Square) (2024)
Closed Access
M. A. Whitehead, Joshua Harvey, Paul E. Sladen, et al.
Research Square (Research Square) (2024)
Closed Access
Hereditary optic neuropathy associated with demyelinating diseases of the central nervous system
Д. Д. Елисеева, A K Kalashnikova, V. V. Bryukhov, et al.
S S Korsakov Journal of Neurology and Psychiatry (2023) Vol. 123, Iss. 7, pp. 122-122
Closed Access | Times Cited: 1
Д. Д. Елисеева, A K Kalashnikova, V. V. Bryukhov, et al.
S S Korsakov Journal of Neurology and Psychiatry (2023) Vol. 123, Iss. 7, pp. 122-122
Closed Access | Times Cited: 1
Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber’s hereditary optic neuropathy
N A Andreeva, Yu K Murakhovskaya, Т.Д. Крылова, et al.
Russian Annals of Ophthalmology (2023) Vol. 139, Iss. 6, pp. 166-166
Closed Access | Times Cited: 1
N A Andreeva, Yu K Murakhovskaya, Т.Д. Крылова, et al.
Russian Annals of Ophthalmology (2023) Vol. 139, Iss. 6, pp. 166-166
Closed Access | Times Cited: 1
