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:
Recent advances and future challenges in gene therapy for hearing loss
Ana E. Amariutei, Jing‐Yi Jeng, Saaïd Safieddine, et al.
Royal Society Open Science (2023) Vol. 10, Iss. 6
Open Access | Times Cited: 9
Ana E. Amariutei, Jing‐Yi Jeng, Saaïd Safieddine, et al.
Royal Society Open Science (2023) Vol. 10, Iss. 6
Open Access | Times Cited: 9
Showing 9 citing articles:
Gene Therapy for Inherited Hearing Loss: Updates and Remaining Challenges
Roni Hahn, Karen B. Avraham
Audiology Research (2023) Vol. 13, Iss. 6, pp. 952-966
Open Access | Times Cited: 11
Roni Hahn, Karen B. Avraham
Audiology Research (2023) Vol. 13, Iss. 6, pp. 952-966
Open Access | Times Cited: 11
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
Tahereh Mohammadian, Fatemeh Zahedipour, Paul Trosien, et al.
Life Sciences (2024) Vol. 348, pp. 122685-122685
Open Access | Times Cited: 4
Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America
Maria Agustina De Rosa, Maria T. Bernardi, Soledad Kleppe, et al.
Genes (2024) Vol. 15, Iss. 2, pp. 178-178
Open Access | Times Cited: 2
Maria Agustina De Rosa, Maria T. Bernardi, Soledad Kleppe, et al.
Genes (2024) Vol. 15, Iss. 2, pp. 178-178
Open Access | Times Cited: 2
Ototoxicity: a high risk to auditory function that needs to be monitored in drug development
Marie-Pierre Pasdelou, Lise Byelyayeva, Susanna Malmström, et al.
Frontiers in Molecular Neuroscience (2024) Vol. 17
Open Access | Times Cited: 2
Marie-Pierre Pasdelou, Lise Byelyayeva, Susanna Malmström, et al.
Frontiers in Molecular Neuroscience (2024) Vol. 17
Open Access | Times Cited: 2
Contemporary directions in the therapy of sensory hearing loss
Anna Rzepakowska, Aleksandra Borowy, Eryk Siedlecki, et al.
Otolaryngologia Polska (2024) Vol. 78, Iss. 4, pp. 29-38
Closed Access | Times Cited: 2
Anna Rzepakowska, Aleksandra Borowy, Eryk Siedlecki, et al.
Otolaryngologia Polska (2024) Vol. 78, Iss. 4, pp. 29-38
Closed Access | Times Cited: 2
Low‐intensity noise exposure takes an essential part in the mechanism of late‐onset hereditary hearing loss caused by Abcc1 mutation
Mengzhu Jiang, Shuai Zhang, Jing Liu, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 462-475
Closed Access
Mengzhu Jiang, Shuai Zhang, Jing Liu, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 462-475
Closed Access
In vivo AAV9-Myo7a gene rescue restores hearing and cholinergic efferent innervation in inner hair cells
Andrew P. O’Connor, Ana E. Amariutei, Alberto Zanella, et al.
JCI Insight (2024) Vol. 9, Iss. 23
Open Access
Andrew P. O’Connor, Ana E. Amariutei, Alberto Zanella, et al.
JCI Insight (2024) Vol. 9, Iss. 23
Open Access
Gene Therapy for Inherited Hearing Loss: Updates and Chal-lenges
Roni Hahn, Karen B. Avraham
(2023)
Open Access | Times Cited: 1
Roni Hahn, Karen B. Avraham
(2023)
Open Access | Times Cited: 1
Inhibition of Pi4kb activity causes malformation of vestibular apparatus in zebrafish by downregulating hey1
Yufei Feng, Jiaqi Zhang, Yuzhen Li, et al.
Gene (2023) Vol. 898, pp. 148105-148105
Closed Access | Times Cited: 1
Yufei Feng, Jiaqi Zhang, Yuzhen Li, et al.
Gene (2023) Vol. 898, pp. 148105-148105
Closed Access | Times Cited: 1
