博士，副主任医师，副研究员。从事斜弱视和小儿眼科疾病诊治十余年，是中华眼科学会小儿眼科与斜视分会委员。2010年博士毕业于中山大学中山眼科中心。曾在美国国立卫生研究院眼科研究所（NIH/NEI）研 究和工作5年。 特长：难治性复杂性斜视，如眼眶骨折后斜视复视、垂直旋转斜视、共同性斜视、A-V斜视、眼球震颤与甲状腺相关眼病后斜视的手术治疗，已经形成明显的优势和特色。开展眼眶骨折后视功能障碍的眼肌手术治疗，近视、远视、弱视矫正、遗传性视网膜色素变性和其他眼遗传病的诊治。特别在眼整形美容方面积累了丰富的临床经验，擅长双重睑、眼袋、上睑下垂等眼部整形美容术。 专著研究：目前主持国家自然基金2项，上海市科研项目1项等，教育部留学回国基金1项。曾获得“江苏省卫生厅科技进步一等奖”，2015年获得“上海市青年东方学者特聘教授”称号，2016年“中华医学会优秀学术论文奖”， 2017年获得“上海交通大学医学院高峰高原计划-研究型医师”称号。目前已经在国内外杂志发表论文13篇，其中SCI文章9篇。 专业擅长：一、斜视、弱视、儿童眼病、遗传性眼病、基因诊断治疗； 二、眼整形美容：包括重睑术（埋线、切开、韩式小切口）、内眦赘皮矫正（开眼角）、眼袋整形手术（内切、外切、眶隔释放泪沟填充）、上睑下垂、小睑裂综合征、眼睑松弛、眼睑内外翻、倒睫、眉下垂、 眼睑退缩、眼睑畸形。 社会荣誉：上海市黄浦区青年联合会委员 欧美同学会医师分会青年委员会常委 中华医学会眼科学分会小儿眼科与斜视学组委员 中国医师协会眼科学分会遗传眼病专委会委员兼秘书 中华医学会眼科学分会小儿眼科与斜视学组委员 NIH中国学者学会上海分会会长 学术论文：1、Lin Li （共同第一作者）, YeFei Wang, XiuHong Qin,Jing Zhang, ZhenZhen Zhang Echinacoside protects retinal ganglion cells from ischemia/ reperfusion-induced injury in the rat retina Molecular Vision 2018 2018; 24:746-758 2、Lin Li （共同第一作者）, Xiaodong Jiao, Ilaria D’Atri. Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa PLoS Genet 2018 2018 Aug 29; 14 (8):e1007504. 3、Zhou YL, Chen CL, Wang YX, Tong Y, Fang XL, Li L （通讯作者）, Wang ZY. Association between polymorphism rs11200638 in the HTRA1 gene and the response to anti-VEGF treatment of exudative AMD: a meta-analysis BMC Ophthalmology 2017 2017;17:97-106 4、Li L （通讯作者）, Chen Y, Jiao X, et al Homozygosity mapping and genetic analysis of autosomal recessive retinal dystrophies in 144 consanguineous Pakistani families Invest Ophthalmol Vis Sci 2017 2017;58:2218-2238 5、David Li, Chongfei Jin, Xiaodong Jiao, Lin Li, S. Amer Riazuddin, and J. Fielding Hejtmancik AIPL1 implicated in the pathogenesis of two cases of autosomal recessive retinal degeneration Molecular Vision 2014 2014; 20: 1–14 6、Huang L, Li S, Xiao X, Jia X, Sun W, Gao Y, Li L, Wang P, Guo X, Zhang Q. Novel GUCA1A mutation identified in a Chinese family with cone-rod dystrophy Neurosci Lett. 2013 2013 ;541:179-83. 7、Lin Li, Xueshan Xiao, Changxian Yi, Xiaodong Jiao, Xiangming Guo, James Fielding Hejtmancik and Qingjiong Zhang. Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome1q31.3–q32.1. Journal of Human Genetics 2012 2012,1–4 8、Li L, Xiao X, Li S, et al. Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis PLoS One 2011 2011; 6(5):e19458. 9、Xueshan Xiao, Wei Li, Panfeng Wang, Lin Li, Shiqiang Li, Xiaoyun Jia,1 Wenmin Sun, Xiangming Guo, Qingjiong Zhang. Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP Molecular Vision 2011 2011; 17:2049-2055. 10、Lin Li, Xueshan Xiao, Shiqiang Li, Xiaodong Jiao, J. Fielding Hejtmancik, Qingjiong Zhang Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutations Molecular Vision 2011 2011; 17:3326-3332 11、Naz S, Riazuddin SA, Li L, Shahid M, Kousar S, Sieving PA, Hejtmancik JF, Riazuddin S. A Novel Locus for Autosomal Recessive Retinitis Pigmentosa in a Consanguineous Pakistani Family Maps to Chromosome 2p. American Journal of Ophthalmology 2010 2010 May; 149(5):861-6. 12、Lin Li （共同第一作者）, Naoki Nakaya, Venkata R.M. Chavali,et al. A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomalrecessive Retinitis Pigmentosa American Journalof Human Genetics 2010 2010;87:400-409 13、Li L, Guan H, Xun P, Zhou J, Gu H. Prevalence and causes of visual impairment among the elderly in Nantong, China Eye 2008 2008 Aug; 22 (8):1069-75. 14、Li L, Guan H, Xun P, et al. An Epidemiological Survey of Cataract among Adults Aged 60 Years and above in Xinchengqiao Block, Nantong. Zhongguo Shi Yong Yan Ke Za Zhi (Chinese Journal of Practical Ophthalmology) 2006 2006, 24(7): 752-757. 15、Li L, Guan H, Zhou J, et al. A cross-sectional survey of blindness and low vision among adults aged 60 years and above in Xinchengqiao Blocks, Nantong Zhonghua Yan ke Za Zhi 2006 2006, 42(9): 802-807