H
He Lin
Researcher at University of Electronic Science and Technology of China
Publications - 21
Citations - 1112
He Lin is an academic researcher from University of Electronic Science and Technology of China. The author has contributed to research in topics: Single-nucleotide polymorphism & Population. The author has an hindex of 14, co-authored 21 publications receiving 945 citations. Previous affiliations of He Lin include Peking Union Medical College & Chinese Academy of Sciences.
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Journal ArticleDOI
Comparison of different samples for 2019 novel coronavirus detection by nucleic acid amplification tests.
Chunbao Xie,Lingxi Jiang,Guo Huang,Hong Pu,Bo Gong,He Lin,Shi Ma,Xuemei Chen,Bo Long,Guo Si,H.J. Yu,Li Jiang,Xingxiang Yang,Yi Shi,Zhenglin Yang +14 more
TL;DR: Nine out of the 19 patients were detected 2019-nCoV infection using oropharyngeal swab samples, and the virus nucleic acid was also detected in eight of these nine patients using stool samples, but none of positive results was identified in the blood and urine samples.
Journal ArticleDOI
Exome sequencing identifies ZNF644 mutations in high myopia.
Yi Shi,Yingrui Li,Dingding Zhang,Hao Zhang,Yuanfeng Li,Fang Lu,Xiaoqi Liu,Fei He,Bo Gong,Li Cai,Ruiqiang Li,Shihuang Liao,Shi Ma,He Lin,Jing Cheng,Hancheng Zheng,Ying Shan,Bin Chen,Jianbin Hu,Xin Jin,Peiquan Zhao,Y W Chen,Yong Zhang,Ying Lin,Xi Li,Fan Y,Huanming Yang,Jun Wang,Zhenglin Yang +28 more
TL;DR: A successful application of exome sequencing is shown to identify a gene for an autosomal dominant disorder, and a gene potentially responsible for high myopia in a monogenic form is identified.
Journal ArticleDOI
Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population
Yi Shi,Jia Qu,Dingding Zhang,Peiquan Zhao,Qingjiong Zhang,Pancy O. S. Tam,Liangdan Sun,Xianbo Zuo,Xiangtian Zhou,Xueshan Xiao,Jianbin Hu,Yuanfeng Li,Li Cai,Xiaoqi Liu,Fang Lu,Shihuang Liao,Bin Chen,Fei He,Bo Gong,He Lin,Shi Ma,Jing Cheng,Jie Zhang,Y W Chen,Fuxin Zhao,Xian Yang,Yuhong Chen,Charles Yang,Dennis S.C. Lam,Xi Li,Fanjun Shi,Zhengzheng Wu,Ying Lin,Jiyun Yang,Shiqiang Li,Yunqing Ren,Anquan Xue,Fan Y,Dean Y. Li,Chi Pui Pang,Xuejun Zhang,Zhenglin Yang +41 more
TL;DR: The results suggest that the variants at 13q12.12 are associated with high myopia in the Han Chinese population, which is one of the leading causes of blindness in the world.
Journal ArticleDOI
Detection of serum IgM and IgG for COVID-19 diagnosis.
Zhong Ling,Zhong Ling,Zhong Ling,Chuan Junlan,Chuan Junlan,Bo Gong,Bo Gong,Bo Gong,Ping Shuai,Yu Zhou,Yu Zhou,Yu Zhou,Yi Zhang,Yi Zhang,Yi Zhang,Zhilin Jiang,Zhilin Jiang,Zhilin Jiang,Dingding Zhang,Dingding Zhang,Dingding Zhang,Xiaoqi Liu,Xiaoqi Liu,Xiaoqi Liu,Shi Ma,Shi Ma,Shi Ma,Yi Huang,He Lin,He Lin,He Lin,Qingwei Wang,Qingwei Wang,Qingwei Wang,Lulin Huang,Lulin Huang,Lulin Huang,Dan Jiang,Dan Jiang,Dan Jiang,Fang Hao,Fang Hao,Fang Hao,Juan Tang,Chunqi Zheng,H.J. Yu,Zhibin Wang,Qi Jiang,Tao Zeng,Mei Luo,Fanwei Zeng,Fanxin Zeng,Jianghai Liu,Tian Junxi,Yu Xu,Long Tengxiang,Kaiju Xu,Xingxiang Yang,Yuping Liu,Yi Shi,Yi Shi,Yi Shi,Li Jiang,Li Jiang,Li Jiang,Zhenglin Yang,Zhenglin Yang,Zhenglin Yang +67 more
TL;DR: Detection of serum IgM and IgG for COVID-19 diagnosis Ling Zhong, Junlan Chuan, Bo Gong, Ping Shuai, Yu Zhou, Yi Zhang, Zhilin Jiang, Dingding Zhang, Xiaoqi Liu, Shi Ma, Yi Huang, He Lin, Qingwei Wang, Lulin Huang, Dan Jiang, Fang Hao, Juan Tang, Chunqi Zheng, Hua Yu, Zhibin Wang, Qi Jiang, Tao Zeng, Mei Luo,
Journal ArticleDOI
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
Yi Shi,Bo Gong,Li Jia Chen,Xianbo Zuo,Xiaoqi Liu,Pancy O. S. Tam,Xiangtian Zhou,Peiquan Zhao,Fang Lu,Jia Qu,Liangdan Sun,Fuxin Zhao,Haoyu Chen,Yiping Zhang,Dingding Zhang,Ying Lin,He Lin,Shi Ma,Jing Cheng,Jiyun Yang,Lulin Huang,Mingzhi Zhang,Xuejun Zhang,Chi Pui Pang,Zhenglin Yang +24 more
TL;DR: Variants of the VIPR2 and SNTB1 genes increase susceptibility to high myopia in Han Chinese, and a genome-wide meta-analysis of single-nucleotide polymorphisms found four SNPs to be associated with this condition.