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Cited by in F6Publishing
For: Valero R, de Castro-Miró M, Jiménez-Ochoa S, Rodríguez-Ezcurra JJ, Marfany G, Gonzàlez-Duarte R. Aberrant Splicing Events Associated to CDH23 Noncanonical Splice Site Mutations in a Proband with Atypical Usher Syndrome 1. Genes (Basel) 2019;10:E732. [PMID: 31546658 DOI: 10.3390/genes10100732] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Velde HM, Reurink J, Held S, Li CHZ, Yzer S, Oostrik J, Weeda J, Haer-wigman L, Yntema HG, Roosing S, Pauleikhoff L, Lange C, Whelan L, Dockery A, Zhu J, Keegan DJ, Farrar GJ, Kremer H, Lanting CP, Damme M, Pennings RJE. Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants. Hum Genet. [DOI: 10.1007/s00439-022-02441-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Chen P, Wang L, Chai Y, Wu H, Yang T. Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness. Front Genet 2021;12:773922. [PMID: 34956325 DOI: 10.3389/fgene.2021.773922] [Reference Citation Analysis]
3 Fry LE, McClements ME, MacLaren RE. Analysis of Pathogenic Variants Correctable With CRISPR Base Editing Among Patients With Recessive Inherited Retinal Degeneration. JAMA Ophthalmol 2021;139:319-28. [PMID: 33507217 DOI: 10.1001/jamaophthalmol.2020.6418] [Cited by in Crossref: 3] [Cited by in F6Publishing: 13] [Article Influence: 3.0] [Reference Citation Analysis]
4 Li J, Xu H, Sun J, Tian Y, Liu D, Qin Y, Liu H, Li R, Neng L, Deng X, Xue B, Yu C, Tang W. Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype. Biomed Res Int 2021;2021:6624744. [PMID: 34258273 DOI: 10.1155/2021/6624744] [Reference Citation Analysis]
5 Bukowska-Olech E, Sowińska-Seidler A, Szczałuba K, Jamsheer A. A novel biallelic splice-site variant in the LRP4 gene causes sclerosteosis 2. Birth Defects Res 2020;112:652-9. [PMID: 32286743 DOI: 10.1002/bdr2.1676] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
6 Nolen RM, Hufnagel RB, Friedman TB, Turriff AE, Brewer CC, Zalewski CK, King KA, Wafa TT, Griffith AJ, Brooks BP, Zein WM. Atypical and ultra-rare Usher syndrome: a review. Ophthalmic Genet 2020;41:401-12. [PMID: 32372680 DOI: 10.1080/13816810.2020.1747090] [Cited by in Crossref: 5] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
7 Toulis V, Cortés-González V, Castro-Miró M, Sallum JF, Català-Mora J, Villanueva-Mendoza C, Ciccioli M, Gonzàlez-Duarte R, Valero R, Marfany G. Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants. Genes (Basel) 2020;11:E378. [PMID: 32244552 DOI: 10.3390/genes11040378] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
8 Al-Kindi MN, Al-Khabouri MJ, Al-Lamki KA, Palombo F, Pippucci T, Romeo G, Al-Wardy NM. In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss. J Genet Eng Biotechnol 2020;18:8. [PMID: 32115674 DOI: 10.1186/s43141-020-0021-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]