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:

Randomized trial of bilateral gene therapy injection for m.11778G>A MT-ND4 Leber optic neuropathy
Nancy J Newman, Patrick Yu‐Wai‐Man, Prem S. Subramanian, et al.
Brain (2022) Vol. 146, Iss. 4, pp. 1328-1341
Open Access | Times Cited: 49

Showing 1-25 of 49 citing articles:

Nucleic Acid Therapeutics: Successes, Milestones, and Upcoming Innovation
Jillian Belgrad, Hassan H. Fakih, Anastasia Khvorova
Nucleic Acid Therapeutics (2024) Vol. 34, Iss. 2, pp. 52-72
Closed Access | Times Cited: 33

Mitochondrial complex I subunit MT-ND1 mutations affect disease progression
Xi Lin, Yanhong Zhou, Lei Xue
Heliyon (2024) Vol. 10, Iss. 7, pp. e28808-e28808
Open Access | Times Cited: 14

Altered Mitochondrial Function in MASLD: Key Features and Promising Therapeutic Approaches
Tatjana Radosavljević, Milica Branković, Janko Samardžić, et al.
Antioxidants (2024) Vol. 13, Iss. 8, pp. 906-906
Open Access | Times Cited: 14

The menace of severe adverse events and deaths associated with viral gene therapy and its potential solution
Artyom Kachanov, Anastasiya Kostyusheva, Sergey Brezgin, et al.
Medicinal Research Reviews (2024) Vol. 44, Iss. 5, pp. 2112-2193
Closed Access | Times Cited: 12

Leber’s hereditary optic neuropathy – current status of idebenone and gene replacement therapies
Thomas Klopstock, Li Zeng, Claudia Priglinger
Medizinische Genetik (2025) Vol. 37, Iss. 1, pp. 57-63
Closed Access | Times Cited: 1

A Comprehensive Review of Clinically Applied Adeno-Associated Virus-Based Gene Therapies for Ocular Disease
Valerie Hinsch, Sanford L. Boye, Sanford L. Boye
Human Gene Therapy (2025)
Closed Access | Times Cited: 1

Gene therapy for mitochondrial disorders
Nandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 1, pp. 145-175
Open Access | Times Cited: 7

Clinical Pharmacology Perspective on Development of Adeno‐Associated Virus Vector‐Based Retina Gene Therapy
Jennifer Lynn Ford, Eleni Karatza, Hardik Mody, et al.
Clinical Pharmacology & Therapeutics (2024) Vol. 115, Iss. 6, pp. 1212-1232
Open Access | Times Cited: 6

Mitochondrial retinopathies and optic neuropathies: the impact of retinal imaging on modern understanding of pathogenesis, diagnosis, and management
Enrico Borrelli, Francesco Bandello, Camiel J. F. Boon, et al.
Progress in Retinal and Eye Research (2024) Vol. 101, pp. 101264-101264
Closed Access | Times Cited: 6

Identification of a novel MT-ND3 variant and restoring mitochondrial function by allotopic expression of MT-ND3 gene
Nurun Nahar Borna, Yoshihito Kishita, Masaru Shimura, et al.
Mitochondrion (2024) Vol. 76, pp. 101858-101858
Closed Access | Times Cited: 5

Single‐cell mitochondrial sequencing reveals low‐frequency mitochondrial mutations in naturally aging mice
Fuyan Liu, Xiaolin Sun, Wei Cai, et al.
Aging Cell (2024) Vol. 23, Iss. 9
Open Access | Times Cited: 5

Developments in the Treatment of Leber Hereditary Optic Neuropathy
Benson Chen, Patrick Yu‐Wai‐Man, Nancy J. Newman
Current Neurology and Neuroscience Reports (2022) Vol. 22, Iss. 12, pp. 881-892
Open Access | Times Cited: 22

Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
Valério Carelli, Nancy J. Newman, Patrick Yu‐Wai‐Man, et al.
Ophthalmology and Therapy (2022) Vol. 12, Iss. 1, pp. 401-429
Open Access | Times Cited: 20

Mitochondria and the eye—manifestations of mitochondrial diseases and their management
Benson Chen, Joshua Harvey, Michael James Gilhooley, et al.
Eye (2023) Vol. 37, Iss. 12, pp. 2416-2425
Open Access | Times Cited: 13

Engineered mitochondria in diseases: mechanisms, strategies, and applications
Mingyang Li, Limin Wu, Haibo Si, et al.
Signal Transduction and Targeted Therapy (2025) Vol. 10, Iss. 1
Open Access

Gene Therapy-Associated Uveitis (GTAU): Understanding and mitigating the adverse immune response in retinal gene therapy
Ryan Purdy, Molly John, AE Bray, et al.
Progress in Retinal and Eye Research (2025), pp. 101354-101354
Open Access

Idebenone vs. rAAV2-ND4 gene therapy in the treatment of Leber’s hereditary optic neuropathy: An indirect comparison meta-analysis
Amr K. Hassan, Hashem Abu Serhan
Indian Journal of Ophthalmology (2025) Vol. 73, Iss. 5, pp. 656-664
Open Access

Clinical Approaches for Mitochondrial Diseases
Seongho Hong, Sanghun Kim, Kyoungmi Kim, et al.
Cells (2023) Vol. 12, Iss. 20, pp. 2494-2494
Open Access | Times Cited: 10

Neuroglobin overexpression in cerebellar neurons of Harlequin mice improves mitochondrial homeostasis and reduces ataxic behavior
Hélène Cwerman‐Thibault, Vassilissa Malko-Baverel, Gwendoline Le Guilloux, et al.
Molecular Therapy (2024) Vol. 32, Iss. 7, pp. 2150-2175
Open Access | Times Cited: 3

Mitochondria in Retinal Ganglion Cells: Unraveling the Metabolic Nexus and Oxidative Stress
Tsai-Hsuan Yang, Eugene Yu‐Chuan Kang, Pei‐Hsuan Lin, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 8626-8626
Open Access | Times Cited: 3

Isolated and Syndromic Genetic Optic Neuropathies: A Review of Genetic and Phenotypic Heterogeneity
Marco Zeppieri, Caterina Gagliano, Marco Di Maita, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3892-3892
Open Access

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

18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal dystrophies and optic neuropathies
Christina Kiel, Fabiola Biasella, Heidi Stöhr, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 3

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