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For: Keats BJ, Savas S. Genetic heterogeneity in Usher syndrome. Am J Med Genet A. 2004;130A:13-16. [PMID: 15368488 DOI: 10.1002/ajmg.a.30052] [Cited by in Crossref: 34] [Cited by in F6Publishing: 29] [Article Influence: 2.0] [Reference Citation Analysis]
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14 Kuroda TS, Fukuda M. Functional Analysis of Slac2-c/MyRIP as a Linker Protein between Melanosomes and Myosin VIIa*[boxs]. Journal of Biological Chemistry 2005;280:28015-22. [DOI: 10.1074/jbc.m501465200] [Cited by in Crossref: 31] [Cited by in F6Publishing: 14] [Article Influence: 1.9] [Reference Citation Analysis]
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16 Pushkin A, Kurtz I. SLC4 base (HCO3 -, CO3 2-) transporters: classification, function, structure, genetic diseases, and knockout models. Am J Physiol Renal Physiol 2006;290:F580-99. [PMID: 16461757 DOI: 10.1152/ajprenal.00252.2005] [Cited by in Crossref: 115] [Cited by in F6Publishing: 101] [Article Influence: 7.7] [Reference Citation Analysis]
17 Colombo L, Montesano G, Sala B, Patelli F, Maltese P, Abeshi A, Bertelli M, Rossetti L. Comparison of 5-year progression of retinitis pigmentosa involving the posterior pole among siblings by means of SD-OCT: a retrospective study. BMC Ophthalmol 2018;18:153. [PMID: 29940899 DOI: 10.1186/s12886-018-0817-z] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
18 Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D. Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. Am J Hum Genet 2016;99:777-84. [PMID: 27588452 DOI: 10.1016/j.ajhg.2016.07.010] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 6.3] [Reference Citation Analysis]
19 Athanasiou D, Aguilà M, Bevilacqua D, Novoselov SS, Parfitt DA, Cheetham ME. The cell stress machinery and retinal degeneration. FEBS Lett. 2013;587:2008-2017. [PMID: 23684651 DOI: 10.1016/j.febslet.2013.05.020] [Cited by in Crossref: 86] [Cited by in F6Publishing: 77] [Article Influence: 10.8] [Reference Citation Analysis]
20 Daiger SP, Bowne SJ, Sullivan LS. Perspective on genes and mutations causing retinitis pigmentosa. Arch Ophthalmol 2007;125:151-8. [PMID: 17296890 DOI: 10.1001/archopht.125.2.151] [Cited by in Crossref: 253] [Cited by in F6Publishing: 236] [Article Influence: 18.1] [Reference Citation Analysis]
21 Cabraja M, Bäurle J. Vestibular ganglion neurons survive hair cell defects in jerker, shaker, and Varitint-waddler mutants and downregulate calretinin expression. J Comp Neurol 2007;504:418-26. [PMID: 17663432 DOI: 10.1002/cne.21453] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
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23 Piatti G, De Santi M, Brogi M, Castorina P, Ambrosetti U. Emerging ciliopathies: Are respiratory cilia compromised in Usher syndrome? American Journal of Otolaryngology 2014;35:340-6. [DOI: 10.1016/j.amjoto.2014.01.010] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 1.4] [Reference Citation Analysis]
24 Phillips JB, Blanco-Sanchez B, Lentz JJ, Tallafuss A, Khanobdee K, Sampath S, Jacobs ZG, Han PF, Mishra M, Titus TA, Williams DS, Keats BJ, Washbourne P, Westerfield M. Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function. Dis Model Mech 2011;4:786-800. [PMID: 21757509 DOI: 10.1242/dmm.006429] [Cited by in Crossref: 37] [Cited by in F6Publishing: 36] [Article Influence: 3.7] [Reference Citation Analysis]
25 McHugh RK, Friedman RA. Genetics of hearing loss: Allelism and modifier genes produce a phenotypic continuum. Anat Rec A Discov Mol Cell Evol Biol 2006;288:370-81. [PMID: 16550584 DOI: 10.1002/ar.a.20297] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 1.7] [Reference Citation Analysis]
26 Dammeyer J. Development and characteristics of children with Usher syndrome and CHARGE syndrome. Int J Pediatr Otorhinolaryngol. 2012;76:1292-1296. [PMID: 22721527 DOI: 10.1016/j.ijporl.2012.05.021] [Cited by in Crossref: 21] [Cited by in F6Publishing: 13] [Article Influence: 2.3] [Reference Citation Analysis]
27 McDermott JH, Molina-Ramírez LP, Bruce IA, Mahaveer A, Turner M, Miele G, Body R, Mahood R, Ulph F, MacLeod R, Harvey K, Booth N, Demain LAM, Wilson P, Black GC, Morton CC, Newman WG. Diagnosing and Preventing Hearing Loss in the Genomic Age. Trends Hear 2019;23:2331216519878983. [PMID: 31621509 DOI: 10.1177/2331216519878983] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
28 Kubota D, Gocho K, Kikuchi S, Akeo K, Miura M, Yamaki K, Takahashi H, Kameya S. CEP250 mutations associated with mild cone-rod dystrophy and sensorineural hearing loss in a Japanese family. Ophthalmic Genet 2018;39:500-7. [PMID: 29718797 DOI: 10.1080/13816810.2018.1466338] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 5.3] [Reference Citation Analysis]
29 Dammeyer J. Children with Usher syndrome: mental and behavioral disorders. Behav Brain Funct 2012;8:16. [PMID: 22449032 DOI: 10.1186/1744-9081-8-16] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 1.3] [Reference Citation Analysis]