Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next‐generation sequencing
Xuejing Bai, Shiyan Nian, Lei Feng, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 7, Iss. 8
Open Access | Times Cited: 13

Showing 13 citing articles:

The natural history, clinical outcomes, and genotype–phenotype relationship of otoferlin-related hearing loss: a systematic, quantitative literature review
Charles L. Ford, William J. Riggs, Tera Quigley, et al.
Human Genetics (2023) Vol. 142, Iss. 10, pp. 1429-1449
Open Access | Times Cited: 17
Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population
Chen‐Chi Wu, Cheng‐Yu Tsai, Yi‐Hsin Lin, et al.
Genes (2019) Vol. 10, Iss. 10, pp. 772-772
Open Access | Times Cited: 41
The clinical and genetic spectrum of twenty-six individuals with hearing loss affected by MYO15A variants
Saeid Morovvati, Mina Mohammadi Sarband, Samaneh Doostmohammadi, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population
Jalal Vallian Broojeni, Arezu Kazemi, Halimeh Rezaei, et al.
PLoS ONE (2023) Vol. 18, Iss. 8, pp. e0289247-e0289247
Open Access | Times Cited: 6
Next‐generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss
Yanbao Xiang, Chenyang Xu, Yunzhi Xu, et al.
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 12
Open Access | Times Cited: 14
Genetic analysis of 106 sporadic cases with hearing loss in the UAE population
Abdelaziz Tlili, Mona Mahfood, Abdullah Al Mutery, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 1
Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss
Akram Sarmadi, Samane Nasrniya, Sina Narrei, et al.
Molecular Biology Reports (2020) Vol. 47, Iss. 7, pp. 5355-5364
Closed Access | Times Cited: 11
Advanced Omics Techniques for Understanding Cochlear Genome, Epigenome and Transcriptome in Health and Disease
Annamaria Tisi, Sakthimala Palaniappan, Mauro Maccarrone
(2023)
Open Access | Times Cited: 2
Advanced Omics Techniques for Understanding Cochlear Genome, Epigenome, and Transcriptome in Health and Disease
Annamaria Tisi, Sakthimala Palaniappan, Mauro Maccarrone
Biomolecules (2023) Vol. 13, Iss. 10, pp. 1534-1534
Open Access | Times Cited: 2
Arterial spin labeling brain MRI study to evaluate the impact of deafness on cerebral perfusion in 79 children before cochlear implantation
Arnaud Coëz, Ludovic Fillon, Ana Saitovitch, et al.
NeuroImage Clinical (2020) Vol. 29, pp. 102510-102510
Open Access | Times Cited: 5
Heterogeneity of MYO15A variants significantly determine the feasibility of acoustic stimulation with hearing aid and cochlear implant
Gina Na, Hye Ji Choi, Sun Young Joo, et al.
Hearing Research (2021) Vol. 404, pp. 108227-108227
Closed Access | Times Cited: 4
Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients
Ying Fu, Shasha Huang, Xue Gao, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Monoallelic loss of the F-actin-binding protein radixin facilitates startle reactivity and pre-pulse inhibition in mice
Torben J. Hausrat, Christian Vogl, Jakob Neef, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 1
Precision Medicine Shows Promise to Advance the Care of Individuals with Hearing Loss
Michelle Pei, Brett M. Colbert, Molly Smea, et al.
Medical Research Archives (2022) Vol. 10, Iss. 11
Open Access | Times Cited: 1
Page 1

Scroll to top