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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:

The Opportunities and Challenges of Gene Therapy for Treatment of Inherited Forms of Vision and Hearing Loss
Emmanuel J. Simons, Ivana Trapani
Human Gene Therapy (2023) Vol. 34, Iss. 17-18, pp. 808-820
Closed Access | Times Cited: 10

Showing 10 citing articles:

PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1F Models
Maryna V. Ivanchenko, Daniel M. Hathaway, Eric M. Mulhall, et al.
Journal of Clinical Investigation (2024)
Open Access | Times Cited: 6
Research hotspots and trends of the <i>SLC26A4</i> gene-related hearing loss from the perspective of knowledge graph
Yue Li, Cheng Wen, Yiding Yu, et al.
Intractable & Rare Diseases Research (2025) Vol. 14, Iss. 1, pp. 55-66
Open Access
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
Retinal gene therapy for Stargardt disease with dual AAV intein vectors is both safe and effective in large animal models
Rita Ferla, Eugenio Pugni, Mariangela Lupo, et al.
Science Advances (2025) Vol. 11, Iss. 13
Closed Access
Gene therapy proves successful in treating hereditary deafness
Ellen Reisinger, Ivana Trapani
The Lancet (2024) Vol. 403, Iss. 10441, pp. 2267-2269
Closed Access | Times Cited: 2
PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1F
Maryna V. Ivanchenko, Daniel M. Hathaway, Eric M. Mulhall, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
The single-cell transcriptomic landscape of the topological differences in mammalian auditory receptors
Xiangyu Ma, Xin Chen, Yuwei Che, et al.
Science China Life Sciences (2024) Vol. 67, Iss. 11, pp. 2398-2410
Closed Access | Times Cited: 1
Non-viral gene therapy for Leber’s congenital amaurosis: progress and possibilities
Latifat Abdulsalam, James Mordecai, Irshad Ahmad
Nanomedicine (2024), pp. 1-14
Closed Access | Times Cited: 1
A patient with 18p11.32-p11.21 deletion have monaural deafness caused by an inadequate haplodose of THOC1: A case report
Geng Ouyang, Enhuan Yi, Huali Qin, et al.
Medicine (2024) Vol. 103, Iss. 30, pp. e39048-e39048
Open Access
Review research designed to investigate gene function and possible impact of specific variants
Moyra Smith
Elsevier eBooks (2024), pp. 315-353
Closed Access
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