Authors: Xu Su, Si Wei, Zhang Yuhang, Huang Yuelin, Li Fuzhen, Shao Jingzhi, Mao Yi, Du Shanshan, Qi Ying, Zhang Fengyan DOI: 10.3760/cma.j.cn115989-20250425-00136 Published: 2026 -03 -10 Citation Xu Su, Si Wei, Zhang Yuhang, et al. Transcriptomics-based analysis of potential pathogenic mechanisms in presenile cataract[J]. Chin J Exp Ophthalmol, 2026, 44(3):260-267. DOI: 10.3760/cma.j.cn115989-20250425-00136. ABSTRACT […]
Tag: Genes
Genetic etiology and clinical strategies of congenital anophthalmia and microphthalmia
Authors: Liao Keren, Shen Yin DOI:10.3760/cma.j.cn115989-20220212-00053 Published: 2024 -10 -10 Citation: Liao Keren, Shen Yin. Genetic etiology and clinical strategies of congenital anophthalmia and microphthalmia[J]. Chin J Exp Ophthalmol, 2024, 42(10):945-951. DOI: 10.3760/cma.j.cn115989-20220212-00053. ABSTRACT […]
Advances in genetic research on complications of pathological myopia
Authors: Lu Qiang, Zhu Xiangjia, Lu Yi DOI:10.3760/cma.j.cn115989-20210429C-00288 Published： 2024 -10 -10 · Citation: Lu Qiang, Zhu Xiangjia, Lu Yi. Advances in genetic research on complications of pathological myopia[J]. Chin J Exp Ophthalmol,2024,42(10): 952-957. DOI: 10.3760/cma.j.cn115989-20210429-00288. ABSTRACT […]
Research progress of keratoconus-related genes and corneal traits
Authors: Cheng Wanyu, Sheng Xunlun DOI: 10.3760/cma.j.cn115989-20210627-00374 Published： 2024 -10 -10 Citation: Cheng Wanyu, Sheng Xunlun. Research progress of keratoconus-related genes and corneal traits[J]. Chin J Exp Ophthalmol, 2024, 42(10):958-962. DOI: 10.3760/cma.j.cn115989-20210627-00374. ABSTRACT [Download […]
Mechanism of curcumin in the treatment of diabetic retinopathy based on network pharmacology and molecular docking
Authors: Du Yuanyuan, Wang Yiyun, Zhao Rong, Zhang Ji, Ji Xiaoyan, Lu Jiayu, Ji Fangfang, Lou Hui, Jiang Ziyuan, Huang Jiang DOI: 10.3760/cma.j.cn115989-20220314-00105 Published 2023-12-10 Cite as Chin J Exp Ophthalmol, 2023, 41(12): 1152-1159. Abstract [Download PDF] [Read Full Text] Objective To […]
Clinical features and genetic variations of Axenfeld-Rieger syndrome
Authors: Wang Qi, Shao Zhengbo, Yuan Huiping DOI: 10.3760/cma.j.cn115989-20200301-00127 Published 2023-09-10 Cite as Chin J Exp Ophthalmol, 2023, 41(9): 920-924. Abstract 【Download PDF】 【Read Full Text】 Axenfeld-Rieger syndrome is a rare autosomal dominant hereditary disease characterized by anterior segment dysgenesis, which may be […]
Clinical features and genetic variations of Axenfeld-Rieger syndrome
Authors: Wang Qi, Shao Zhengbo, Yuan Huiping DOI: 10.3760/cma.j.cn115989-20200301-00127 Published 2023-09-10 Cite as Chin J Exp Ophthalmol, 2023, 41(9): 920-924. Abstract 【Download PDF】 【Read Full Text】 Axenfeld-Rieger syndrome is a rare autosomal dominant hereditary disease characterized by anterior segment dysgenesis, which may be […]
Attaching importance to the genetic diagnosis of early-onset high myopia
Author: Sheng Xunlun DOI: 10.3760/cma.j.cn115989-20210915-00517 Published 2022-03-10 Cite asChin J Exp Ophthalmol, 2022, 40(3): 193-198. Abstract [View PDF] [Read Full Text] According to the onset age, high myopia can be divided into late-onset high myopia (loHM) and early-onset high myopia (eoHM). Numerous genetic studies have […]