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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:

Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function
Lucy A Dunbar, Pranav Patni, Carlos Aguilar, et al.
EMBO Molecular Medicine (2019) Vol. 11, Iss. 9
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges
Sedigheh Delmaghani, A. Amraoui
Journal of Clinical Medicine (2020) Vol. 9, Iss. 7, pp. 2309-2309
Open Access | Times Cited: 100
Myosin-based nucleation of actin filaments contributes to stereocilia development critical for hearing
Zane G. Moreland, Fangfang Jiang, Carlos Aguilar, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss
Clara Mendia, Thibault Peineau, Mina Zamani, et al.
Molecular Therapy (2024) Vol. 32, Iss. 3, pp. 800-817
Open Access | Times Cited: 6
A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens
Wei Liu, Åsa Johansson, Helge Rask‐Andersen, et al.
BMC Medicine (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 31
Origin and evolution of microvilli
Mylan Ansel, Kausthubh Ramachandran, G.K. Dey, et al.
Biology of the Cell (2024) Vol. 116, Iss. 11
Open Access | Times Cited: 4
Accelerated Hydration Site Localization and Thermodynamic Profiling
Florian B. Hinz, Matthew R. Masters, James Nguyen, et al.
Journal of Chemical Information and Modeling (2025)
Open Access
Molecular identity of the mechanotransduction machinery in inner ear hair cells and mechanotransduction-linked hearing loss
Yanyan Jia, Huawei Li, Wenyan Li
Fundamental Research (2025)
Open Access
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
Barbara Vona, Neda Mazaheri, Sheng‐Jia Lin, et al.
Human Genetics (2021) Vol. 140, Iss. 6, pp. 915-931
Open Access | Times Cited: 23
Mechanoelectrical transduction-related genetic forms of hearing loss
Jinsei Jung, Ulrich Müller
Current Opinion in Physiology (2023) Vol. 32, pp. 100632-100632
Open Access | Times Cited: 7
Non-syndromic hearing loss: clinical and diagnostic challenges
Barbara Vona, Julia Doll, Michaela A. H. Hofrichter, et al.
Medizinische Genetik (2020) Vol. 32, Iss. 2, pp. 117-129
Closed Access | Times Cited: 19
Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing
Sherylanne Newton, Fanbo Kong, Adam J. Carlton, et al.
PLoS Genetics (2022) Vol. 18, Iss. 1, pp. e1009937-e1009937
Open Access | Times Cited: 10
Usher syndrome IIIA: a review of the disorder and preclinical research advances in therapeutic approaches
Azmi Marouf, Benjamin Johnson, Kumar N. Alagramam
Human Genetics (2022) Vol. 141, Iss. 3-4, pp. 759-783
Closed Access | Times Cited: 9
gEAR: gene Expression Analysis Resource portal for community-driven, multi-omic data exploration
Joshua Orvis, Brian Gottfried, Jayaram Kancherla, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 13
Myosin-driven Nucleation of Actin Filaments Drives Stereocilia Development Critical for Hearing
Zane G. Moreland, Fangfang Jiang, Carlos Aguilar, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 12
Application of gene therapy in auditory system diseases
Chun-jiang Wei, Weijia Kong, Zuhong He
STEMedicine (2020) Vol. 1, Iss. 1, pp. e17-e17
Open Access | Times Cited: 7
Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies
Regie Lyn P. Santos‐Cortez, Talitha Karisse L. Yarza, Tori C. Bootpetch, et al.
Genes (2021) Vol. 12, Iss. 4, pp. 566-566
Open Access | Times Cited: 7
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice
Güney Bademci, María Lachgar, Mangesh Deokar, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 26
Open Access | Times Cited: 4
Defects in hair cells disrupt the development of auditory peripheral circuitry
Riley T. Bottom, Yijun Xu, Caroline Siebald, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Biallelic mutation ofCLRN2causes non-syndromic hearing loss in humans
Barbara Vona, Neda Mazaheri, Sheng‐Jia Lin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 3
Analysis of Bone Mineral Density and Bithermal Caloric Test Results in Unilateral Idiopathic Benign Paroxysmal Positional Vertigo Patients
Xiuwen Jiang, Haibing Ding, Bin Shen, et al.
Otology & Neurotology (2022) Vol. 43, Iss. 7, pp. e780-e786
Closed Access | Times Cited: 2
Novel Cellular Stress Models with Implications in Understanding and Treating ENT Pathologies
Naresh K. Panda, Maryada Sharma, Anurag Ramavat, et al.
(2022), pp. 139-180
Closed Access | Times Cited: 1
Génétique et physiologie cellulaire
Christine Petit
L’annuaire du Collège de France (2023) Vol. 120, pp. 153-157
Open Access
Sex differences, cross-ancestry generalizability, and noise-smoking interactions in the polygenic architecture of hearing loss in adults
Flavio De Angelis, Oana A. Zeleznik, Frank R. Wendt, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
An Update on Autosomal Recessive Hearing Loss and Loci Involved in It
Mahbobeh Koohiyan, Masrooreh Hoseini, Fatemeh Azadegan‐Dehkordi
Indian Journal of Otology (2022) Vol. 28, Iss. 1, pp. 6-17
Closed Access
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