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Ophthalmic Genetics|August 10, 2022
The importance of genome sequencing: unraveling SSBP1 variant missed by exome sequencingJae Won Jun, Yuri Seo, Sueng-Han Han, et al.Ophthalmic Genetics|March 17, 2023
A paradigm shift in the treatment of refractory angle closure glaucoma in a patient with X-linked juvenile retinoschisisSirisha Senthil, Deepika C Parameswarappa, Jeyapoorani BalasubramannianOphthalmic Genetics|March 1, 2023
Harel Yoon syndrome: a novel mutation in ATAD3A gene and expansion of the clinical spectrumCaroline Atef Tawfik, Raghda Zaitoun, Aliaa Ahmed FaragOphthalmic Genetics|February 2, 2023
A case of Aicardi syndrome associated with duplication event of Xp22 including SHOXLeyla Yavuz Saricay, Sandra Hoyek, Ayush Ashit Parikh, et al.Ophthalmic Genetics|February 10, 2023
RPGRIP1-related retinal disease presenting as isolated cone dysfunctionArif O KhanOphthalmic Genetics|March 11, 2025
Unusual fundus lesion in mosaic neurofibromatosis type 2Michael H Berry, David F Skanchy, Steven M Archer, et al.Ophthalmic Genetics|February 27, 2025
Unilateral posterior subcapsular cataract and lenticonus in a girl with Bloom's syndrome - report of a rare caseSandra Chandramouli, Minnulekshmi Reghukumar, Kalpana NarendranOphthalmic Genetics|February 25, 2025
Association between vitamin D receptor polymorphisms and diabetic retinopathy in Uygur Chinese with type 2 diabetesLi Li, Xueyi Chen, Xianglong YiOphthalmic Genetics|February 14, 2025
Reproductive counseling and decision making in females affected by X-linked inherited retinal disease: perspectives from carriersRebecca Clark, Haider Sarwar, Leland Wong, et al.Ophthalmic Genetics|January 24, 2025
Comprehensive insights into circular RNAs, miRNAs, and lncRNAs as biomarkers in retinoblastomaMahsa Fakeri, Fatemeh Shakoul, Seyyed Mohammad Yaghoubi, et al.Pageof 185