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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:

Progress in Gene Editing Tools and Their Potential for Correcting Mutations Underlying Hearing and Vision Loss
Catherine Botto, Deniz Dalkara, A. Amraoui
Frontiers in Genome Editing (2021) Vol. 3
Open Access | Times Cited: 22

Showing 22 citing articles:

The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification
Sedigheh Delmaghani, A. Amraoui
Human Genetics (2022) Vol. 141, Iss. 3-4, pp. 709-735
Open Access | Times Cited: 75
Retinitis Pigmentosa: Novel Therapeutic Targets and Drug Development
Kevin Y. Wu, Merve Kulbay, Dana Toameh, et al.
Pharmaceutics (2023) Vol. 15, Iss. 2, pp. 685-685
Open Access | Times Cited: 46
Promising Strategies for Preserving Adult Endothelium Health and Reversing Its Dysfunction: From Liquid Biopsy to New Omics Technologies and Noninvasive Circulating Biomarkers
Carmela Rita Balistreri
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 14, pp. 7548-7548
Open Access | Times Cited: 23
Vestibular Deficits in Deafness: Clinical Presentation, Animal Modeling, and Treatment Solutions
Audrey Maudoux, Sandrine Vitry, A. Amraoui
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 20
Gene therapy in pediatrics – Clinical studies and approved drugs (as of 2023)
Tahereh Mohammadian, Fatemeh Zahedipour, Paul Trosien, et al.
Life Sciences (2024) Vol. 348, pp. 122685-122685
Open Access | Times Cited: 4
Advancing precision ear medicine: leveraging animal models for disease insights and therapeutic innovations
Sandrine Vitry, Clara Mendia, Audrey Maudoux, et al.
Mammalian Genome (2025)
Open Access
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
Poly(β-amino ester) Nanoparticles Modified with a Rabies-Virus-Derived Peptide for the Delivery of ASCL1 across a 3D In Vitro Model of the Blood–Brain Barrier
Tina Rodgers, Nicolás Muzzio, Andrea Valero, et al.
ACS Applied Nano Materials (2023) Vol. 6, Iss. 7, pp. 6299-6311
Open Access | Times Cited: 9
The Genomics of Auditory Function and Disease
Shahar Taiber, Kathleen Gwilliam, Ronna Hertzano, et al.
Annual Review of Genomics and Human Genetics (2022) Vol. 23, Iss. 1, pp. 275-299
Open Access | Times Cited: 14
The Role of Pericytes in Inner Ear Disorders: A Comprehensive Review
Antonino Maniaci, Marilena Briglia, Fabio Allia, et al.
Biology (2024) Vol. 13, Iss. 10, pp. 802-802
Open Access | Times Cited: 2
Rare immune diseases paving the road for genome editing-based precision medicine
Mara Pavel-Dinu, Šimon Borna, Rosa Bacchetta
Frontiers in Genome Editing (2023) Vol. 5
Open Access | Times Cited: 6
Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F
Sehar Riaz, Saumil Sethna, Todd Duncan, et al.
Molecular Therapy (2023) Vol. 31, Iss. 12, pp. 3490-3501
Closed Access | Times Cited: 6
Optogenetics: Illuminating the Future of Hearing Restoration and Understanding Auditory Perception
Namit Kant Singh, Balaji Ramamourthy, Neemu Hage, et al.
Current Gene Therapy (2024) Vol. 24, Iss. 3, pp. 208-216
Closed Access | Times Cited: 1
Promising Strategies for Preserving Adult Endothelium Health and Reversing Its Dysfunction: From the Liquid Biopsy to New Omics Technologies and Non-invasive Circulating Biomarkers
Carmela Rita Balistreri
(2022)
Open Access | Times Cited: 7
Distributional comparison of different AAV vectors after unilateral cochlear administration
Shuang Han, Zhijiao Xu, Shengyi Wang, et al.
Gene Therapy (2023)
Closed Access | Times Cited: 3
Gene Therapy for Rhodopsin Mutations
Alfred S. Lewin, Wayne C. Smith
Cold Spring Harbor Perspectives in Medicine (2022) Vol. 12, Iss. 9, pp. a041283-a041283
Open Access | Times Cited: 3
Somatic Genome Editing: Technical Challenges and Ethical Appraisal
Francis J. O’Keeffe, Aurélia Alphonse, George L. Mendz
European Journal of Medical and Health Research (2024) Vol. 2, Iss. 3, pp. 239-247
Open Access
Implementing next-generation sequencing for diagnosis and management of hereditary hearing impairment: a comprehensive review
Cheng‐Yu Tsai, Jacob Shujui Hsu, Pei‐Lung Chen, et al.
Expert Review of Molecular Diagnostics (2024) Vol. 24, Iss. 9, pp. 753-765
Closed Access
Optimization of HITI-Mediated Gene Insertion for Rhodopsin and Peripherin-2 in Mouse Rod Photoreceptors: Targeting Dominant Retinitis Pigmentosa
Akishi Onishi, Yuji Tsunekawa, Michiko Mandai, et al.
Investigative Ophthalmology & Visual Science (2024) Vol. 65, Iss. 13, pp. 38-38
Open Access
Gene therapy for hereditary hearing loss
Zeming Fu, Liping Zhao, Yingyuan Guo, et al.
Hearing Research (2024) Vol. 455, pp. 109151-109151
Closed Access
G protein-coupled receptors in cochlea: Potential therapeutic targets for hearing loss
Xiangyu Ma, Jiamin Guo, Yaoyang Fu, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 2
Genetic, molecular and biochemical basis of the auditory aging: lessons from experimental models
Blanca Cervantes, Jose M. Bermúdez‐Muñoz, Carmen Ruiz-García, et al.
Auditio (2022) Vol. 6
Open Access | Times Cited: 1
Efficient workflow for validating homology-independent targeted integration-mediated gene insertion in rod photoreceptor cells to treat dominant-negative mutations causing retinitis pigmentosa
Akishi Onishi, Yuji Tsunekawa, Michiko Mandai, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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