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Cited by in F6Publishing
For: Tian L, Chen C, Song Y, Zhang X, Xu K, Xie Y, Jin ZB, Li Y. Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations. Invest Ophthalmol Vis Sci 2022;63:5. [PMID: 35657619 DOI: 10.1167/iovs.63.6.5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Chang H, Zhang X, Xu K, Li N, Xie Y, Yan W, Li Y. Phenotype-Based Genetic Analysis Reveals Missing Heritability of KIF11-Related Retinopathy: Clinical and Genetic Findings. Genes (Basel) 2023;14. [PMID: 36672954 DOI: 10.3390/genes14010212] [Reference Citation Analysis]
2 Tian L, Zhang XH, Xu K, Li Y. Induced pluripotent stem cell line BIOi003-A from a patient with ABCA4-associated retinal dystrophy carrying compound heterozygous c.(1222C>T;2919-884G>T) variants in ABCA4. Stem Cell Res 2022;64:102894. [PMID: 35973334 DOI: 10.1016/j.scr.2022.102894] [Reference Citation Analysis]