Professor | Xi Wu | Asia Growth Partners

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Name	Xi Wu
Contact Information	wuxi0901@163.com
Language ability	Chinese, English
Province	Shanghai

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Name

Xi Wu

Contact Information

wuxi0901@163.com

Language ability

Chinese, English

Province

Shanghai

University/Lab Affiliation and Title	Shanghai Jiao Tong University
Faculty	Bio-X Research Institute
Academic Background & Achievements	2004-2008 Bachelor: Shanghai Jiao Tong University 2008-2014 Doctorate: Shanghai Jiao Tong University 2014-2016 Postdoctoral: Shanghai Jiao Tong University

University/Lab Affiliation and Title

Shanghai Jiao Tong University

Faculty

Bio-X Research Institute

Academic Background & Achievements

2004-2008 Bachelor: Shanghai Jiao Tong University
2008-2014 Doctorate: Shanghai Jiao Tong University
2014-2016 Postdoctoral: Shanghai Jiao Tong University

Areas of Focus	Genetics and pharmacogenomics of mental disorders Pathogenic mechanisms of birth defects
Publications	Microdeletion and Microduplication Analysis of Chinese Conotruncal Defects Patients with Targeted Array Comparative Genomic Hybridization, Xiaohui Gong, Xi Wu, Xiaojing Ma, Dandan Wu, Ting Zhang, Li He, Shengying Qin, Xiaotian Li, 2013 Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk, Xi Wu, Qingqing Xu, Liang Guo, Chuanting Yu, Yuyu Xiong, Zhiyun Wei, Ran Huo, Shengtian Li, Lu Shen, Jiamin Niu, Lu Liu, Yi Lin, Lin He, Shengying Qin, 2013 Quantitative assessment of the effect of LRRK2 exonic variants on the risk of Parkinson's disease: a meta-analysis, Xi Wu, KeFu Tang, Yang Li, YuYu Xiong, Lu Shen, ZhiYun Wei, KeJun Zhou, Jia Min Niu, Xia Han, Lun Yang, GuoYin Feng, Lin He, ShengYing Qin, 2012 Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population, Qingqing Xu, Xi Wu, Mo Li, Hailiang Huang, Camelia Minica, Zhenghui Yi, Guoqiang Wang, Lu Shen, Qinghe Xing, Yongyong Shi, Lin He, Shengying Qin, 2016 GSK-3β and BDNF genes may not be associated with venlafaxine treatment response in Chinese of Han ethnicity, Sun Q, Yuan F, Ren D, Ma G, Yang F, Wu X, He L, He G, 2019 p.E95K mutation in Indian hedgehog causing brachydactyly type A1 impairs IHH/Gli1 downstream transcriptional regulation, Shen L, Ma G, Shi Y, Ruan Y, Yang X, Wu X, Xiong Y, Wan C, Yang C, Cai L, Xiong L, Gong X, He L, Qin S, 2019 Association study between ABCB1, ABCB6 and ABCG1 polymorphisms and major depressive disorder in the Chinese Han population, Ma G, Huang X, Bi Y, Ren D, Xu F, Sun Q, Zhang R, Hu J, Niu W, Guo Z, Yuan R, Yuan F, Wu X, Cao Y, Yang F, Wang L, Li W, Yu T, He L, Liu J, He G, Li X, 2018 Study of the association between Schizophrenia and microduplication at the 16p11.2 locus in the Han Chinese population, Zhou W, Shi Y, Li F, Wu X, Huai C, Shen L, Yi Z, He L, Liu C, Qin S, 2018

Areas of Focus

Genetics and pharmacogenomics of mental disorders
Pathogenic mechanisms of birth defects

Publications

Microdeletion and Microduplication Analysis of Chinese Conotruncal Defects Patients with Targeted Array Comparative Genomic Hybridization, Xiaohui Gong, Xi Wu, Xiaojing Ma, Dandan Wu, Ting Zhang, Li He, Shengying Qin, Xiaotian Li, 2013
Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk, Xi Wu, Qingqing Xu, Liang Guo, Chuanting Yu, Yuyu Xiong, Zhiyun Wei, Ran Huo, Shengtian Li, Lu Shen, Jiamin Niu, Lu Liu, Yi Lin, Lin He, Shengying Qin, 2013
Quantitative assessment of the effect of LRRK2 exonic variants on the risk of Parkinson's disease: a meta-analysis, Xi Wu, KeFu Tang, Yang Li, YuYu Xiong, Lu Shen, ZhiYun Wei, KeJun Zhou, Jia Min Niu, Xia Han, Lun Yang, GuoYin Feng, Lin He, ShengYing Qin, 2012
Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population, Qingqing Xu, Xi Wu, Mo Li, Hailiang Huang, Camelia Minica, Zhenghui Yi, Guoqiang Wang, Lu Shen, Qinghe Xing, Yongyong Shi, Lin He, Shengying Qin, 2016
GSK-3β and BDNF genes may not be associated with venlafaxine treatment response in Chinese of Han ethnicity, Sun Q, Yuan F, Ren D, Ma G, Yang F, Wu X, He L, He G, 2019
p.E95K mutation in Indian hedgehog causing brachydactyly type A1 impairs IHH/Gli1 downstream transcriptional regulation, Shen L, Ma G, Shi Y, Ruan Y, Yang X, Wu X, Xiong Y, Wan C, Yang C, Cai L, Xiong L, Gong X, He L, Qin S, 2019
Association study between ABCB1, ABCB6 and ABCG1 polymorphisms and major depressive disorder in the Chinese Han population, Ma G, Huang X, Bi Y, Ren D, Xu F, Sun Q, Zhang R, Hu J, Niu W, Guo Z, Yuan R, Yuan F, Wu X, Cao Y, Yang F, Wang L, Li W, Yu T, He L, Liu J, He G, Li X, 2018
Study of the association between Schizophrenia and microduplication at the 16p11.2 locus in the Han Chinese population, Zhou W, Shi Y, Li F, Wu X, Huai C, Shen L, Yi Z, He L, Liu C, Qin S, 2018

Genetics Pharmacogenomics Mental Disorders Birth Defects Pathogenic Mechanisms Research Chinese Population Genomic Variants Treatment Response Association Studies

Shengying Qin - Shanghai Jiao Tong University

Lin He - Shanghai Jiao Tong University

Yongyong Shi - Shanghai Jiao Tong University

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