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Frontiers in Psychiatry|September 26, 2022
Depression in multiple system atrophy: Views on pathological, clinical and imaging aspectsQiuyi Lv, Yuxin Pan, Xing Chen, et al.
Investigative Ophthalmology & Visual Science|June 27, 2015
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1Jiali Li, Bei Gao, Liping Guan, et al.
Cardiology|August 3, 2012
Beneficial effects of high-dose atorvastatin pretreatment on renal function in patients with acute ST-segment elevation myocardial infarction undergoing emergency percutaneous coronary interventionWei Li, Xianghua Fu, Yanbo Wang, et al.
Human Genetics|June 19, 2014
Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencingYan Xu, Liping Guan, Tao Shen, et al.
Investigative Ophthalmology & Visual Science|January 8, 2024
Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 FamiliesDongwei Guo, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|April 9, 2026
Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndromeDi Zhu, Yuxi Zheng, Yi Jiang, et al.
Brain : a Journal of Neurology|October 18, 2024
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genesYuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
Cardiovascular Therapeutics|September 8, 2012
Efficacy and safety of standard-dose versus half-dose tirofiban in patients with non-ST elevation acute coronary syndromes undergoing early percutaneous coronary interventionWei Li, Xianghua Fu, Haiwei Xue, et al.
Human Genetics|September 21, 2022
Truncation mutations in MYRF underlie primary angle closure glaucomaJiamin Ouyang, Wenmin Sun, Huangxuan Shen, et al.
Investigative Ophthalmology & Visual Science|March 14, 2023
The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High MyopiaYi Jiang, Lin Zhou, Yingwei Wang, et al.
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