Association between genetic polymorphisms of cadherin 23 and noise-induced hearing loss: a meta-analysis-Reference-Cited by-同舟云学术

Association between genetic polymorphisms of cadherin 23 and noise-induced hearing loss: a meta-analysis

Published:2022-01-02 Issue:1 Volume:49 Page:41-53
ISSN:0301-4460
Container-title:Annals of Human Biology
language:en
Short-container-title:Annals of Human Biology

Author:

Wu Zhi-Dan¹^ORCID,Lu Jun-Qi²,Du Wen-Jing¹,Wu Shan¹

Affiliation:

1. Guangdong Provincial Engineering Research Center of Public Health Detection and Assessment, School of Public Health, Guangdong Pharmaceutical University, Guangzhou, China

2. Yuexiu District Center for Disease Control and Prevention, Guangzhou, China

Funder

GuangDong Basic and Applied Basic Research Foundation

GuangDong Medical Scientific Research Foundation

Guangdong Undergraduate Training Project for Innovation and Entrepreneurship

Project for Innovation and Strong School of Department of Education of Guangdong Province

Publisher

Informa UK Limited

Subject

Public Health, Environmental and Occupational Health,Genetics,Aging,Physiology,Epidemiology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03014460.2021.2016963

Reference39 articles.

1. Operating Characteristics of a Rank Correlation Test for Publication Bias

2. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

3. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

4. Bias in meta-analysis detected by a simple, graphical test

5. Hearing loss prevalence and years lived with disability, 1990–2019: findings from the Global Burden of Disease Study 2019

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1. Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing Loss;Genes;2024-04-29

2. Polymorphisms and NIHL: a systematic review and meta-analyses;Frontiers in Cellular Neuroscience;2023-06-15