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   Kaoru Fujinami et al, 2020, American Journal of Medical Genetics Part C: Seminars in Medical Genetics CrossRef
2. Whole exome sequencing analysis identifies novel Stargardt disease-related gene mutations in Chinese Stargardt disease and retinitis pigmentosa patients
   Tsz Kin Ng et al, 2022, Eye CrossRef
3. Recent Developments on the major genes involved in retinitis pigmentosa
   Anogeianakis George A et al, 2020, IP International Journal of Ocular Oncology and Oculoplasty CrossRef
4. Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies
   Belal Azab et al, 2019, Canadian Journal of Ophthalmology CrossRef
5. Alterations of functional connectivity density in a Chinese family with a mild phenotype associated with a novel inherited variant of SCN8A
   Qiong Zhu et al, 2020, Epilepsy & Behavior CrossRef
6. Identification of novel PROM1 mutations responsible for autosomal recessive maculopathy with rod-cone dystrophy
   Jian Liang et al, 2019, Graefe's Archive for Clinical and Experimental Ophthalmology CrossRef
7. Identification of two novel PRPF31 mutations in Chinese families with non‐syndromic autosomal dominant retinitis pigmentosa
   Li Cao et al, 2020, Molecular Genetics & Genomic Medicine CrossRef
8. Integrative Analysis of CD133 mRNA in Human Cancers Based on Data Mining
   Gui-Min Wen et al, 2019, Stem Cell Reviews and Reports CrossRef
9. Foveal hypoplasia in parents of patients with albinism
   R. Lejoyeux et al, 2022, Ophthalmic Genetics CrossRef