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Yi Guo
yiguo@csu.edu.cn
Chinese, English
Hunan
Central South University
Life Sciences
  • 2009-2012 PhD: Central South University
  • 2000-2002 Master's: Central South University
  • 1994-1998 Bachelor's: Hunan University
  • 2021.09-present - Central South University - Professor
  • 2013.09-2021.08 - Central South University - Associate Professor
  • 2005.01-2007.08 - MD Anderson Cancer Center, USA - Assistant Researcher
  • 2003.09-2013.08 - Central South University - Lecturer
  • 1998.07-2003.08 - Central South University - Teaching Assistant
  • 2018: Main lecturer for the Hunan Province Quality Online Open Course 'Medical Literature Retrieval' (Ranked 3rd)
  • 2009: Main lecturer for the National Quality Course 'Literature Information Retrieval' (Ranked 4th)
Genetic localization of hereditary diseases, gene cloning, pathogenic site identification, susceptibility gene screening, and bioinformatics research
  • Identifying a BRCA2 p. L1908RfsX2 mutation in a Han-Chinese family with breast cancer, Yi Guo, Peng Wang, Xiaorong Li, Shaihong Zhu, Hongbo Xu, Shizhou Li, Hao Deng, Lamei Yuan, 2019
  • COL1A2 p.Gly1066Val mutation identified in a Chinese family with osteogenesis imperfecta type I, Mingyuan Wang, Yi Guo, Pengfei Rong, Hongbo Xu, Lina Gong, Hao Deng, Lamei Yuan, 2019
  • Identification of a novel keratin 9 missense mutation in a Chinese family with epidermolytic palmoplantar keratoderma, Heng Xiao, Yi Guo, Junhui Yi, Hong Xia, Hongbo Xu, Lamei Yuan, Pengzhi Hu, Zhijian Yang, Zhenghao He, Hongwei Lu, Hao Deng, 2018
  • PINK1 p.K520RfsX3 Mutation Identified in a Chinese Family with Early-onset Parkinson’s disease, Peng Wang, Yi Guo, Chengyuan Song, Yiming Liu, Hao Deng, 2018
  • Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing, Hao Deng, Ting Tan, Quanyong He, Qiongfen Lin, Zhijian Yang, Anding Zhu, Liping Guan, Jinjing Xiao, Zhi Song, Yi Guo, 2017
  • TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease, Yi Guo, Ting Tan, Xiong Deng, Zhi Song, Zhijian Yang, Yan Yang, Hao Deng, 2015
  • Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing, Yi Guo, Jinzhong Yuan, Hui Liang, Jingjing Xiao, Hongbo Xu, Lamei Yuan, Kai Gao, Bin Wu, Yongchang Tang, Xiaorong Li, Hao Deng, 2014
  • Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutation, Yi Guo, Zhi Song, Hongbo Xu, Junhui Yi, Wen Zheng, Hong Xiang, Xiong Deng, Hongwei Lv, Kai Gao, Yong Qi, Hao Deng, 2014
Genetics Hereditary Diseases Gene Cloning Pathogenic Sites Gene Screening Bioinformatics Disease Localization Susceptibility Genes Molecular Genetics Genomic Medicine

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