导师姓名： 李琳 专业代码： 100212
性别： 女 专业名称： 眼科学
培养单位： 附属第九人民医院 三级学科/
专业领域：
导师类型： 硕士生导师 专业学位导师：
联系方式： jannetlee1300@163.com
邮编： 200011 邮箱地址： jannetlee1300@163.com

研究方向 (点击浏览详细信息)
眼外肌疾病和遗传性眼病研究

社会任职
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（筹）委员兼秘书
中国医师协会眼科学分会遗传眼病专委会（筹）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****学会上海分会会长

科研项目 项目编号项目名称课题来源起止年月批准经费承担职责
** 氯离子通道基因RP32突变致视网膜色素变性的机制研究 国家自然基金面上项目 2017-01~2020-12 61万元 课题负责人
100200 眼外肌纤维化家系的致病基因筛查和分析 上海交通大学医学院眼视光学专项建设子课题 2016-03~2019-03 10万元 课题负责人
教外司留〔2015〕1098号 遗传性视网膜色素变性的基因诊断 教育部留学回国人员科研启动基金 2015-06~2018-12 3万元 课题负责人
** TALENs新技术敲除和敲入znf513基因建立与研究视网膜色素变性的模型与发病机制 国家自然科学基金青年基金项目 2014-01~2016-12 23万元 课题负责人

学术论文 作者论文标题期刊名出版年卷期页码
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
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):e**.
Zhou YL, Chen CL, Wang YX, Tong Y, Fang XL, Li L （通讯作者）, Wang ZY. Association between polymorphism rs** in the HTRA1 gene and the response to anti-VEGF treatment of exudative AMD: a meta-analysis BMC Ophthalmology 2017 2017;17:97-106
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
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
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.
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
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.
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.
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
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.
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
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.
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.
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