Genetics of Usher Syndrome: New Insights From a Meta-analysis-Reference-Cited by-同舟云学术

Genetics of Usher Syndrome: New Insights From a Meta-analysis

Published:2019-01 Issue:1 Volume:40 Page:121-129
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Jouret Guillaume,Poirsier Céline,Spodenkiewicz Marta,Jaquin Clémence,Gouy Evan,Arndt Carl,Labrousse Marc,Gaillard Dominique,Doco-Fenzy Martine,Lebre Anne-Sophie

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Sensory Systems,Otorhinolaryngology

Reference75 articles.

1. Albrecht von Graefe (1828-1870): founder of scientific ophthalmology;Tan;Singapore Med J,2007

2. Usher's syndrome—deafness and progressive blindness: Clinical cases, prevention, theory and literature survey;Vernon;J Chronic Dis,1969

3. Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing;Yoshimura;J Hum Genet,2016

4. Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment studyCommentary: Universal newborn hearing screening: implications for coordinating and developing services for deaf and hearing-impaired children;Fortnum;BMJ,2001

5. Usher syndrome and cochlear implantation;Loundon;Otol Neurotol,2003

Cited by 60 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel compound heterozygous variant of MYO7A in Usher syndrome type 1;Experimental Eye Research;2024-10

2. CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History;Investigative Ophthalmology & Visual Science;2024-07-17

3. Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health;Frontiers in Genetics;2024-04-22

4. Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia;Annals of Human Genetics;2024-03-22

5. Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population;Genetic Testing and Molecular Biomarkers;2024-03-01