Professor | Yi Guo | Asia Growth Partners

Name	Yi Guo
Contact Information	yiguo@csu.edu.cn
Language ability	Chinese, English
Province	Hunan

Name

Yi Guo

Contact Information

yiguo@csu.edu.cn

Language ability

Chinese, English

Province

Hunan

University/Lab Affiliation and Title	Central South University
Faculty	Life Sciences
Academic Background & Achievements	2009-2012 PhD: Central South University 2000-2002 Master's: Central South University 1994-1998 Bachelor's: Hunan University
Work Experience	2021-present - Central South University - Professor 2013-2021 - Central South University - Associate Professor 2005-2007 - MD Anderson Cancer Center, USA - Assistant Researcher 2003-2013 - Central South University - Lecturer 1998-2003 - Central South University - Teaching Assistant
Awards	2018: Main lecturer for the online open course 'Medical Literature Retrieval' (Ranked 3rd) - Hunan Province 2009: Main lecturer for the national quality course 'Literature Information Retrieval' (Ranked 4th)

University/Lab Affiliation and Title

Central South University

Faculty

Life Sciences

Academic Background & Achievements

2009-2012 PhD: Central South University
2000-2002 Master's: Central South University
1994-1998 Bachelor's: Hunan University

Work Experience

2021-present - Central South University - Professor
2013-2021 - Central South University - Associate Professor
2005-2007 - MD Anderson Cancer Center, USA - Assistant Researcher
2003-2013 - Central South University - Lecturer
1998-2003 - Central South University - Teaching Assistant

Awards

2018: Main lecturer for the online open course 'Medical Literature Retrieval' (Ranked 3rd) - Hunan Province
2009: Main lecturer for the national quality course 'Literature Information Retrieval' (Ranked 4th)

Areas of Focus	Genetic localization of hereditary diseases, gene cloning, pathogenic site identification, susceptibility gene screening, and bioinformatics research
Publications	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

Areas of Focus

Genetic localization of hereditary diseases, gene cloning, pathogenic site identification, susceptibility gene screening, and bioinformatics research

Publications

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

Genetic Localization Hereditary Diseases Gene Cloning Pathogenic Site Identification Susceptibility Genes Screening Bioinformatics Research Gene Screening

Xiong Dehui - Central South University

Yudong Cai - Shanghai University

Yanping Long - Southern University of Science and Technology

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