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For: 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: 5] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Robillard KN, de Vrieze E, van Wijk E, Lentz JJ. Altering gene expression using antisense oligonucleotide therapy for hearing loss. Hearing Research 2022. [DOI: 10.1016/j.heares.2022.108523] [Reference Citation Analysis]
2 Shughoury A, Ciulla TA, Bakall B, Pennesi ME, Kiss S, Cunningham ET Jr. Genes and Gene Therapy in Inherited Retinal Disease. Int Ophthalmol Clin 2021;61:3-45. [PMID: 34584043 DOI: 10.1097/IIO.0000000000000377] [Reference Citation Analysis]
3 Dlugaiczyk J. Rare Disorders of the Vestibular Labyrinth: of Zebras, Chameleons and Wolves in Sheep's Clothing. Laryngorhinootologie 2021;100:S1-S40. [PMID: 34352900 DOI: 10.1055/a-1349-7475] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Wafa TT, Faridi R, King KA, Zalewski C, Yousaf R, Schultz JM, Morell RJ, Muskett J, Turriff A, Tsilou E, Griffith AJ, Friedman TB, Zein WM, Brewer CC. Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndrome. Clin Genet 2021;99:226-35. [PMID: 33089500 DOI: 10.1111/cge.13868] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
5 Igelman AD, Ku C, da Palma MM, Georgiou M, Schiff ER, Lam BL, Sankila EM, Ahn J, Pyers L, Vincent A, Ferraz Sallum JM, Zein WM, Oh JK, Maldonado RS, Ryu J, Tsang SH, Gorin MB, Webster AR, Michaelides M, Yang P, Pennesi ME. Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic Genet 2021;:1-10. [PMID: 34223797 DOI: 10.1080/13816810.2021.1946704] [Reference Citation Analysis]
6 Whatley M, Francis A, Ng ZY, Khoh XE, Atlas MD, Dilley RJ, Wong EYM. Usher Syndrome: Genetics and Molecular Links of Hearing Loss and Directions for Therapy. Front Genet 2020;11:565216. [PMID: 33193648 DOI: 10.3389/fgene.2020.565216] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
7 Radhakrishnan R, Dronamraju VR, Leung M, Gruesen A, Solanki AK, Walterhouse S, Roehrich H, Song G, da Costa Monsanto R, Cureoglu S, Martin R, Kondkar AA, van Kuijk FJ, Montezuma SR, Knöelker HJ, Hufnagel RB, Lobo GP. The role of motor proteins in photoreceptor protein transport and visual function. Ophthalmic Genet 2022;:1-16. [PMID: 35470760 DOI: 10.1080/13816810.2022.2062391] [Reference Citation Analysis]
8 Singh J, Sharma M, Jain N, Aftab I, Vikram N, Singh TP, Sharma P, Sharma S. Lactoferrin and its nano-formulations in rare eye diseases. Indian J Ophthalmol 2022;70:2328-34. [PMID: 35791114 DOI: 10.4103/ijo.IJO_303_22] [Reference Citation Analysis]
9 Castiglione A, Möller C. Usher Syndrome. Audiology Research 2022;12:42-65. [DOI: 10.3390/audiolres12010005] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
10 Dinculescu A, Link BA, Saperstein DA. Retinal Gene Therapy for Usher Syndrome: Current Developments, Challenges, and Perspectives. Int Ophthalmol Clin 2021;61:109-24. [PMID: 34584048 DOI: 10.1097/IIO.0000000000000378] [Reference Citation Analysis]
11 Fowler NH, El-Rashedy MI, Chishti EA, Vander Kooi CW, Maldonado RS. Multimodal imaging and genetic findings in a case of ARSG-related atypical Usher syndrome. Ophthalmic Genet 2021;42:338-43. [PMID: 33629623 DOI: 10.1080/13816810.2021.1891552] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Delmaghani S, El-Amraoui A. The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification. Hum Genet 2022. [PMID: 35353227 DOI: 10.1007/s00439-022-02448-7] [Reference Citation Analysis]