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Cited by in F6Publishing
For: 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: 2] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Nguyen Tran MT, Kc R, Hewitt AW. A Taxonomic and Phylogenetic Classification of Diverse Base Editors. CRISPR J 2022. [PMID: 35244489 DOI: 10.1089/crispr.2021.0095] [Reference Citation Analysis]
2 Piotter E, Mcclements ME, Maclaren RE. The Scope of Pathogenic ABCA4 Mutations Targetable by CRISPR DNA Base Editing Systems—A Systematic Review. Front Genet 2022;12:814131. [DOI: 10.3389/fgene.2021.814131] [Reference Citation Analysis]
3 Piotter E, McClements ME, MacLaren RE. Therapy Approaches for Stargardt Disease. Biomolecules 2021;11:1179. [PMID: 34439845 DOI: 10.3390/biom11081179] [Reference Citation Analysis]
4 Bellingrath JS, McClements ME, Kaukonen M, Fischer MD, MacLaren RE. In Silico Analysis of Pathogenic CRB1 Single Nucleotide Variants and Their Amenability to Base Editing as a Potential Lead for Therapeutic Intervention. Genes (Basel) 2021;12:1908. [PMID: 34946856 DOI: 10.3390/genes12121908] [Reference Citation Analysis]
5 Bansal M, Acharya S, Sharma S, Phutela R, Rauthan R, Maiti S, Chakraborty D. CRISPR Cas9 based genome editing in inherited retinal dystrophies. Ophthalmic Genet 2021;42:365-74. [PMID: 33821751 DOI: 10.1080/13816810.2021.1904421] [Reference Citation Analysis]
6 Liu W, Li L, Jiang J, Wu M, Lin P. Applications and challenges of CRISPR-Cas gene-editing to disease treatment in clinics. Precis Clin Med 2021;4:179-91. [PMID: 34541453 DOI: 10.1093/pcmedi/pbab014] [Reference Citation Analysis]
7 da Costa BL, Levi SR, Eulau E, Tsai YT, Quinn PMJ. Prime Editing for Inherited Retinal Diseases. Front Genome Ed 2021;3:775330. [PMID: 34901928 DOI: 10.3389/fgeed.2021.775330] [Reference Citation Analysis]
8 Schneider N, Sundaresan Y, Gopalakrishnan P, Beryozkin A, Hanany M, Levanon EY, Banin E, Ben-Aroya S, Sharon D. Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities. Prog Retin Eye Res 2021;:101029. [PMID: 34839010 DOI: 10.1016/j.preteyeres.2021.101029] [Reference Citation Analysis]
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