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For: Géléoc GGS, El-Amraoui A. Disease mechanisms and gene therapy for Usher syndrome. Hear Res 2020;394:107932. [PMID: 32199721 DOI: 10.1016/j.heares.2020.107932] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 14.0] [Reference Citation Analysis]
Number Citing Articles
1 de Joya EM, Colbert BM, Tang PC, Lam BL, Yang J, Blanton SH, Dykxhoorn DM, Liu X. Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy. Int J Mol Sci 2021;22:3910. [PMID: 33920085 DOI: 10.3390/ijms22083910] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Toms M, Pagarkar W, Moosajee M. Usher syndrome: clinical features, molecular genetics and advancing therapeutics. Ther Adv Ophthalmol 2020;12:2515841420952194. [PMID: 32995707 DOI: 10.1177/2515841420952194] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
3 Mauriac SA, Géléoc GSG. A hop, skip, and a jump to evade USH2A deaf-blindness mutations. Mol Ther 2021;29:2391-3. [PMID: 34297918 DOI: 10.1016/j.ymthe.2021.07.008] [Reference Citation Analysis]
4 Ben-Yosef T, Asia Batsir N, Ali Nasser T, Ehrenberg M. Retinal dystrophy as part of TTC21B-associated ciliopathy. Ophthalmic Genet 2021;42:329-33. [PMID: 33599192 DOI: 10.1080/13816810.2021.1888131] [Reference Citation Analysis]
5 Delmaghani S, El-Amraoui A. Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges. J Clin Med 2020;9:E2309. [PMID: 32708116 DOI: 10.3390/jcm9072309] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 14.0] [Reference Citation Analysis]
6 Bahena P, Daftarian N, Maroofian R, Linares P, Villalobos D, Mirrahimi M, Rad A, Doll J, Hofrichter MAH, Koparir A, Röder T, Han S, Sabbaghi H, Ahmadieh H, Behboudi H, Villanueva-Mendoza C, Cortés-Gonzalez V, Zamora-Ortiz R, Kohl S, Kuehlewein L, Darvish H, Alehabib E, Arenas-Sordo ML, Suri F, Vona B, Haaf T. Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment. Hum Genet 2021. [PMID: 34148116 DOI: 10.1007/s00439-021-02303-1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Renauld JM, Basch ML. Congenital Deafness and Recent Advances Towards Restoring Hearing Loss. Curr Protoc 2021;1:e76. [PMID: 33780161 DOI: 10.1002/cpz1.76] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Tatour Y, Ben-Yosef T. Syndromic Inherited Retinal Diseases: Genetic, Clinical and Diagnostic Aspects. Diagnostics (Basel) 2020;10:E779. [PMID: 33023209 DOI: 10.3390/diagnostics10100779] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
9 Moshiri A. Animals Models of Inherited Retinal Disease. Int Ophthalmol Clin 2021;61:113-30. [PMID: 34196320 DOI: 10.1097/IIO.0000000000000368] [Reference Citation Analysis]
10 Al Mutery A, Mahfood M, Chouchen J, Tlili A. Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries. Hum Genet 2021. [PMID: 34338889 DOI: 10.1007/s00439-021-02323-x] [Reference Citation Analysis]
11 Fuster-García C, García-Bohórquez B, Rodríguez-Muñoz A, Aller E, Jaijo T, Millán JM, García-García G. Usher Syndrome: Genetics of a Human Ciliopathy. Int J Mol Sci 2021;22:6723. [PMID: 34201633 DOI: 10.3390/ijms22136723] [Reference Citation Analysis]
12 Warnecke A, Giesemann A. Embryology, Malformations, and Rare Diseases of the Cochlea. Laryngorhinootologie 2021;100:S1-S43. [PMID: 34352899 DOI: 10.1055/a-1349-3824] [Reference Citation Analysis]
13 Zhu J, Choi JW, Ishibashi Y, Isgrig K, Grati M, Bennett J, Chien W. Refining surgical techniques for efficient posterior semicircular canal gene delivery in the adult mammalian inner ear with minimal hearing loss. Sci Rep 2021;11:18856. [PMID: 34552193 DOI: 10.1038/s41598-021-98412-y] [Reference Citation Analysis]