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Cited by in F6Publishing
For: Lam BL, Leroy BP, Black G, Ong T, Yoon D, Trzupek K. Genetic testing and diagnosis of inherited retinal diseases. Orphanet J Rare Dis 2021;16:514. [PMID: 34906171 DOI: 10.1186/s13023-021-02145-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Lopour MQR, Schimmenti LA, Boczek NJ, Kearney HM, Drack AV, Brodsky MC. Alström syndrome caused by maternal uniparental disomy. Am J Ophthalmol Case Rep 2023;29:101745. [PMID: 36636630 DOI: 10.1016/j.ajoc.2022.101745] [Reference Citation Analysis]
2 Jimenez HJ, Procopio RA, Thuma TBT, Marra MH, Izquierdo N, Klufas MA, Nagiel A, Pennesi ME, Pulido JS. Signal Peptide Variants in Inherited Retinal Diseases: A Multi-Institutional Case Series. IJMS 2022;23:13361. [DOI: 10.3390/ijms232113361] [Reference Citation Analysis]
3 Lisbjerg K, Bertelsen M, Lyng Forman J, Grønskov K, Prener Holtan J, Kessel L. Disease progression of retinitis pigmentosa caused by PRPF31 variants in a Nordic population: a retrospective study with up to 36 years follow-up. Ophthalmic Genet 2022;:1-8. [PMID: 36164253 DOI: 10.1080/13816810.2022.2123006] [Reference Citation Analysis]
4 Lando L, Borooah S. Late-Onset Retinal Degeneration: Clinical Perspectives. OPTH 2022;Volume 16:3225-3246. [DOI: 10.2147/opth.s362691] [Reference Citation Analysis]
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