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:

Therapeutic Options in Hereditary Optic Neuropathies
Giulia Amore, Martina Romagnoli, Michele Carbonelli, et al.
Drugs (2020) Vol. 81, Iss. 1, pp. 57-86
Open Access | Times Cited: 81

Showing 26-50 of 81 citing articles:

Gene therapy for Leber hereditary optic neuropathy
Marco Battista, Valério Carelli, Leonardo Bottazzi, et al.
Expert Opinion on Biological Therapy (2024) Vol. 24, Iss. 6, pp. 521-528
Closed Access | Times Cited: 2

5-HT3 Receptors on Mitochondria Influence Mitochondrial Function
Santosh T. R. B. Rao, Ilona Turek, Julian Ratcliffe, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8301-8301
Open Access | Times Cited: 6

Optimisation of AAV-NDI1 Significantly Enhances Its Therapeutic Value for Correcting Retinal Mitochondrial Dysfunction
Naomi Chadderton, Arpad Palfi, Daniel Maloney, et al.
Pharmaceutics (2023) Vol. 15, Iss. 2, pp. 322-322
Open Access | Times Cited: 5

Clinical Insights into Mitochondrial Neurodevelopmental and Neurodegenerative Disorders: Their Biosignatures from Mass Spectrometry-Based Metabolomics
Haorong Li, Martine Uittenbogaard, Ling Hao, et al.
Metabolites (2021) Vol. 11, Iss. 4, pp. 233-233
Open Access | Times Cited: 12

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

Recognizing Leber’s Hereditary Optic Neuropathy to avoid delayed diagnosis and misdiagnosis
Chiara La Morgia, Maria Lucia Cascavilla, Anna Maria De Negri, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access | Times Cited: 1

Leber hereditary optic neuropathy: new and emerging therapies
Pamela Davila-Siliezar, Michael Carter, Dan Miléa, et al.
Current Opinion in Ophthalmology (2022) Vol. 33, Iss. 6, pp. 574-578
Closed Access | Times Cited: 7

Solutions to a Radical Problem: Overview of Current and Future Treatment Strategies in Leber’s Hereditary Opic Neuropathy
Samuel J. Spiegel, Alfredo A. Sadun
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 21, pp. 13205-13205
Open Access | Times Cited: 7

Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives
Camille Peron, Alessandra Maresca, Andrea Cavaliere, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 9

Cell-Based Neuroprotection of Retinal Ganglion Cells in Animal Models of Optic Neuropathies
Yue Hu, Lynn Michelle Grodzki, Susanne Bartsch, et al.
Biology (2021) Vol. 10, Iss. 11, pp. 1181-1181
Open Access | Times Cited: 8

Leber’s Hereditary Optic Neuropathy (LHON): Clinical Experience and Outcomes after Long-Term Idebenone Treatment
George Baltă, Georgiana Cristache, Andreea Diana Barac, et al.
Life (2023) Vol. 13, Iss. 10, pp. 2000-2000
Open Access | Times Cited: 3

Neuromuscular disease: 2022 update.
Marta Margeta
DOAJ (DOAJ: Directory of Open Access Journals) (2022) Vol. 3
Closed Access | Times Cited: 5

Leber Hereditary Optic Neuropathy: Molecular Pathophysiology and Updates on Gene Therapy
Sheng-Chu Chi, Hui‐Chen Cheng, An-Guor Wang
Biomedicines (2022) Vol. 10, Iss. 8, pp. 1930-1930
Open Access | Times Cited: 5

Cell Therapy Replacement for Retinal and Optic Nerve Diseases: Cell Sources, Clinical Trials and Challenges
Rosa M. Coco, Salvador Pastor‐Idoate, José Carlos Pastor Jimeno
(2021)
Open Access | Times Cited: 7

PhNR and peripapillary RNFL changes in Leber hereditary optic neuropathy with m.G11778A mutation
Qingmei Miao, Yufang Cheng, Hongmei Zheng, et al.
Mitochondrion (2023) Vol. 70, pp. 111-117
Open Access | Times Cited: 2

Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
Giulia Amore, Veria Vacchiano, Chiara La Morgia, et al.
Journal of Neurology (2022) Vol. 270, Iss. 1, pp. 559-564
Open Access | Times Cited: 3

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

Advances in research on Leber’s hereditary optic neuropathy
Qingru Zhou, Zhenhui Liu, Jiawei Sun, et al.
Ocular genetics and omics. (2024) Vol. 1, pp. 100002-100002
Open Access

Mitochondrial DNA variants in a cohort from Argentina with suspected Leber’s hereditary optic neuropathy (LHON)
Paula Buonfiglio, Sebastián Menazzi, Liliana Francipane, et al.
PLoS ONE (2023) Vol. 18, Iss. 2, pp. e0275703-e0275703
Open Access | Times Cited: 1

Photoreceptor changes in Leber hereditary optic neuropathy with m.G11778A mutation
Qingmei Miao, Hongmei Zheng, Jiajia Yuan, et al.
International Journal of Ophthalmology (2023) Vol. 16, Iss. 6, pp. 928-932
Open Access | Times Cited: 1

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

Case report: Mutations in DNAJC30 causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals
Toby Charles Major, Eszter Sára Arany, Katherine Schon, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 1

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