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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:

Clinical Characteristics and Current Therapies for Inherited Retinal Degenerations
José‐Alain Sahel, Katia Marazova, Isabelle Audo
Cold Spring Harbor Perspectives in Medicine (2014) Vol. 5, Iss. 2, pp. a017111-a017111
Open Access | Times Cited: 198

Showing 1-25 of 198 citing articles:

Anosmia—A Clinical Review
Sanne Boesveldt, Elbrich M. Postma, Duncan Boak, et al.
Chemical Senses (2017) Vol. 42, Iss. 7, pp. 513-523
Open Access | Times Cited: 334
Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR
Jasmina Cehajic‐Kapetanovic, Kanmin Xue, Cristina Martínez-Fernández de la Cámara, et al.
Nature Medicine (2020) Vol. 26, Iss. 3, pp. 354-359
Open Access | Times Cited: 283
Managing Bardet–Biedl Syndrome—Now and in the Future
Elizabeth Forsythe, Joanna Kenny, Chiara Bacchelli, et al.
Frontiers in Pediatrics (2018) Vol. 6
Open Access | Times Cited: 182
Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia
Kanmin Xue, Jasleen K. Jolly, Alun R. Barnard, et al.
Nature Medicine (2018) Vol. 24, Iss. 10, pp. 1507-1512
Open Access | Times Cited: 163
Mechanisms of Photoreceptor Death in Retinitis Pigmentosa
Fay Newton, Roly Megaw
Genes (2020) Vol. 11, Iss. 10, pp. 1120-1120
Open Access | Times Cited: 160
Gene Editing for CEP290 -Associated Retinal Degeneration
Eric Pierce, Tomas S. Alemán, Thiran Jayasundera, et al.
New England Journal of Medicine (2024) Vol. 390, Iss. 21, pp. 1972-1984
Closed Access | Times Cited: 60
Oral Antioxidant and Lutein/Zeaxanthin Supplements Slow Geographic Atrophy Progression to the Fovea in Age-Related Macular Degeneration
Tiarnán D L Keenan, Elvira Agrón, Pearse A. Keane, et al.
Ophthalmology (2024) Vol. 132, Iss. 1, pp. 14-29
Closed Access | Times Cited: 23
Microglial phagocytosis and activation underlying photoreceptor degeneration is regulated by CX3CL1‐CX3CR1 signaling in a mouse model of retinitis pigmentosa
Matthew Zabel, Lian Zhao, Yikui Zhang, et al.
Glia (2016) Vol. 64, Iss. 9, pp. 1479-1491
Open Access | Times Cited: 161
Diagnostic exome sequencing in 266 Dutch patients with visual impairment
Lonneke Haer‐Wigman, Wendy AG van Zelst-Stams, Rolph Pfundt, et al.
European Journal of Human Genetics (2017) Vol. 25, Iss. 5, pp. 591-599
Open Access | Times Cited: 133
RPGR: Its role in photoreceptor physiology, human disease, and future therapies
Roly Megaw, Dinesh C. Soares, Alan F. Wright
Experimental Eye Research (2015) Vol. 138, pp. 32-41
Open Access | Times Cited: 111
Combination of cGMP analogue and drug delivery system provides functional protection in hereditary retinal degeneration
Eleonora Vighi, Dragana Trifunović, Patricia Veiga‐Crespo, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 13
Open Access | Times Cited: 105
Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9‐year period
Nicole Weisschuh, Carolin D. Obermaier, Florian Battke, et al.
Human Mutation (2020) Vol. 41, Iss. 9, pp. 1514-1527
Open Access | Times Cited: 104
Ocular Neurodegenerative Diseases: Interconnection between Retina and Cortical Areas
Nicoletta Marchesi, Foroogh Fahmideh, Federica Boschi, et al.
Cells (2021) Vol. 10, Iss. 9, pp. 2394-2394
Open Access | Times Cited: 90
Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes
Yilai Shu, Tao Yong, Zhengmin Wang, et al.
Human Gene Therapy (2016) Vol. 27, Iss. 9, pp. 687-699
Open Access | Times Cited: 89
Gene-Based Therapeutics for Inherited Retinal Diseases
Beau J. Fenner, Tien‐En Tan, Veluchamy A. Barathi, et al.
Frontiers in Genetics (2022) Vol. 12
Open Access | Times Cited: 45
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy
Marianthi Karali, Francesco Testa, Valentina Di Iorio, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 43
The first genetic landscape of inherited retinal dystrophies in Portuguese patients identifies recurrent homozygous mutations as a frequent cause of pathogenesis
Virginie G. Peter, Karolina Kamińska, Cristina Santos, et al.
PNAS Nexus (2023) Vol. 2, Iss. 3
Open Access | Times Cited: 28
Gene-agnostic therapeutic approaches for inherited retinal degenerations
Molly C. John, Joel Quinn, Monica L. Hu, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 15
Open Access | Times Cited: 25
Breaking genetic shackles: The advance of base editing in genetic disorder treatment
Fang Xu, Caiyan Zheng, Weihui Xu, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 9
Development of visual Neuroprostheses: trends and challenges
Eduardo Fernández
Bioelectronic Medicine (2018) Vol. 4, Iss. 1
Open Access | Times Cited: 81
RNA delivery biomaterials for the treatment of genetic and rare diseases
Weiyu Zhao, Xucheng Hou, Olivia G. Vick, et al.
Biomaterials (2019) Vol. 217, pp. 119291-119291
Open Access | Times Cited: 72
Molecular Therapies for Inherited Retinal Diseases—Current Standing, Opportunities and Challenges
Irene Vázquez-Domínguez, Alejandro Garanto, Rob W.J. Collin
Genes (2019) Vol. 10, Iss. 9, pp. 654-654
Open Access | Times Cited: 69
Gene Therapy and Stem Cell Transplantation in Retinal Disease: The New Frontier
Robert E. MacLaren, Jean Bennett, Steven D. Schwartz
Ophthalmology (2016) Vol. 123, Iss. 10, pp. S98-S106
Open Access | Times Cited: 68
Antisense Oligonucleotide Screening to Optimize the Rescue of the Splicing Defect Caused by the Recurrent Deep-Intronic ABCA4 Variant c.4539+2001G>A in Stargardt Disease
Alejandro Garanto, Lonneke Duijkers, Tomasz Z. Tomkiewicz, et al.
Genes (2019) Vol. 10, Iss. 6, pp. 452-452
Open Access | Times Cited: 59
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