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For: Vona B, Doll J, Hofrichter MAH, Haaf T, Varshney GK. Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing loss. Hear Res 2020;397:107906. [PMID: 32063424 DOI: 10.1016/j.heares.2020.107906] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Trpchevska N, Freidin MB, Broer L, Oosterloo BC, Yao S, Zhou Y, Vona B, Bishop C, Bizaki-Vallaskangas A, Canlon B, Castellana F, Chasman DI, Cherny S, Christensen K, Concas MP, Correa A, Elkon R, Mengel-From J, Gao Y, Giersch ABS, Girotto G, Gudjonsson A, Gudnason V, Heard-Costa NL, Hertzano R, Hjelmborg JVB, Hjerling-Leffler J, Hoffman HJ, Kaprio J, Kettunen J, Krebs K, Kähler AK, Lallemend F, Launer LJ, Lee IM, Leonard H, Li CM, Lowenheim H, Magnusson PKE, van Meurs J, Milani L, Morton CC, Mäkitie A, Nalls MA, Nardone GG, Nygaard M, Palviainen T, Pratt S, Quaranta N, Rämö J, Saarentaus E, Sardone R, Satizabal CL, Schweinfurth JM, Seshadri S, Shiroma E, Shulman E, Simonsick E, Spankovich C, Tropitzsch A, Lauschke VM, Sullivan PF, Goedegebure A, Cederroth CR, Williams FMK, Nagtegaal AP; Estonian Biobank Research Team. Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss. Am J Hum Genet 2022;109:1077-91. [PMID: 35580588 DOI: 10.1016/j.ajhg.2022.04.010] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
2 Alkowari M, Espino-Guarch M, Daas S, Abdelrahman D, Hasan W, Krishnamoorthy N, Sathappan A, Sheehan P, Panhuys NV, The Qatar Genome Program Research Consortium, Estivill X. Functional Characterization of the MYO6 Variant p.E60Q in Non-Syndromic Hearing Loss Patients. Int J Mol Sci 2022;23:3369. [PMID: 35328790 DOI: 10.3390/ijms23063369] [Reference Citation Analysis]
3 Han E, Lee DH, Park S, Rah YC, Park H, Choi JW, Choi J. Noise-induced hearing loss in zebrafish model: Characterization of tonotopy and sex-based differences. Hearing Research 2022. [DOI: 10.1016/j.heares.2022.108485] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Lopez-Escamez JA, Cheng AG, Grill E, Liu TC. Editorial: Epidemiology and Genetics of Vestibular Disorders. Front Neurol 2021;12:743379. [PMID: 34630314 DOI: 10.3389/fneur.2021.743379] [Reference Citation Analysis]
5 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: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
6 Bassani S, Beelen E, Rossel M, Voisin N, Morgan A, Arribat Y, Chatron N, Chrast J, Cocca M, Delprat B, Faletra F, Giannuzzi G, Guex N, Machavoine R, Pradervand S, Smits JJ, van de Kamp JM, Ziegler A, Amati F, Marlin S, Kremer H, Locher H, Maurice T, Gasparini P, Girotto G, Reymond A. Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss. Hum Mol Genet 2021:ddab145. [PMID: 34059922 DOI: 10.1093/hmg/ddab145] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
7 Colón-Cruz L, Rodriguez-Morales R, Santana-Cruz A, Cantres-Velez J, Torrado-Tapias A, Lin SJ, Yudowski G, Kensler R, Marie B, Burgess SM, Renaud O, Varshney GK, Behra M. Cnr2 Is Important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors. Front Mol Neurosci 2021;14:624265. [PMID: 33958989 DOI: 10.3389/fnmol.2021.624265] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Parkinson L, Stawicki TM. alms1 mutant zebrafish do not show hair cell phenotypes seen in other cilia mutants. PLoS One 2021;16:e0246844. [PMID: 33793549 DOI: 10.1371/journal.pone.0246844] [Reference Citation Analysis]
9 de Bruijn SE, Fadaie Z, Cremers FPM, Kremer H, Roosing S. The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss. Int J Mol Sci 2021;22:2943. [PMID: 33799353 DOI: 10.3390/ijms22062943] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
10 Frings S. Modellorganismen in der Sinnesphysiologie. Die Sinne der Tiere 2021. [DOI: 10.1007/978-3-662-63233-8_17] [Reference Citation Analysis]
11 Salazar-Silva R, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague E, Mingroni-Netto RC. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Hum Mol Genet 2021;29:3691-705. [PMID: 33326993 DOI: 10.1093/hmg/ddaa240] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
12 Parkinson L, Stawicki TM. alms1 mutant zebrafish do not show hair cell phenotypes seen in other cilia mutants.. [DOI: 10.1101/2020.11.13.381954] [Reference Citation Analysis]
13 Rad A, Schade-Mann T, Gamerdinger P, Yanus GA, Schulte B, Müller M, Imyanitov EN, Biskup S, Löwenheim H, Tropitzsch A, Vona B. Aberrant COL11A1 splicing causes prelingual autosomal dominant nonsyndromic hearing loss in the DFNA37 locus. Hum Mutat 2021;42:25-30. [PMID: 33169910 DOI: 10.1002/humu.24136] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
14 Colon-cruz L, Rodriguez-morales R, Santana-cruz A, Cantres-velez J, Torrado-tapias A, Yudowski G, Kensler R, Marie B, Burgess S, Renaud O, Varshney GK, Behra M. Cnr2 is important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors.. [DOI: 10.1101/2020.08.18.253120] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 da Silva RS, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague E, Netto RCM. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.. [DOI: 10.1101/2020.06.07.138909] [Reference Citation Analysis]