Professor | 胡正茂 | 数字化转型顾问

Name	胡正茂
Contact Information	huzhengmao@sklmg.edu.cn
Language ability	中文, 英语
Province	湖南省

Name

胡正茂

Contact Information

huzhengmao@sklmg.edu.cn

Language ability

中文, 英语

Province

湖南省

University/Lab Affiliation and Title	中南大学
Faculty	Life Sciences
Academic Background & Achievements	2004/09-2007/07 中南大学/医学遗传学国家重点实验室，遗传学博士 2001/09-2004/07 中南大学/医学遗传学国家重点实验室，遗传学硕士 1990/09-1994/07 湖南师范大学生物系，生物学学士
Work Experience	2019/01-至今 - 中南大学生命科学学院，副院长 2016/10-至今 - 中南大学/医学遗传学研究中心，研究员 2012/12-2013/12 - 伊利诺伊大学芝加哥分校，访问学者 2010/10-2016/09 - 中南大学/医学遗传学国家重点实验室，副研究员 2007/07-2010/09 - 中南大学，助理研究员 1994/07-2001/08 - 湖南省食用菌研究所，实习研究员/助理研究员

University/Lab Affiliation and Title

中南大学

Faculty

Life Sciences

Academic Background & Achievements

2004/09-2007/07 中南大学/医学遗传学国家重点实验室，遗传学博士
2001/09-2004/07 中南大学/医学遗传学国家重点实验室，遗传学硕士
1990/09-1994/07 湖南师范大学生物系，生物学学士

Work Experience

2019/01-至今 - 中南大学生命科学学院，副院长
2016/10-至今 - 中南大学/医学遗传学研究中心，研究员
2012/12-2013/12 - 伊利诺伊大学芝加哥分校，访问学者
2010/10-2016/09 - 中南大学/医学遗传学国家重点实验室，副研究员
2007/07-2010/09 - 中南大学，助理研究员
1994/07-2001/08 - 湖南省食用菌研究所，实习研究员/助理研究员

Areas of Focus	儿童孤独症的遗传基础及机制研究高度近视的遗传基础及机制研究
Publications	The autism risk gene CNTN4 modulates dendritic spine formation., R. Zhao, T. Zhu, Q. Liu, Q. Tian, M. Wang, J. Chen, D. Tong, B. Yu, H. Guo, K. Xia, Z. Qiu, Z. Hu, 2021 Slc39a5 Dysfunction Impairs Extracellular Matrix Synthesis in High Myopia Pathogenesis., S. Dong, Q. Tian, T. Zhu, K. Wang, G. Lei, Y. Liu, H. Xiong, L. Shen, M. Wang, R. Zhao, H. Wu, B. Li, Q. Zhang, Y. Yao, H. Guo, K. Xia, L. Xia, Z. Hu, 2021 Biallelic Loss-of-Function Variants in Nemf Cause Central Nervous System Impairment and Axonal Polyneuropathy., A. Ahmed, M. Wang, G. Bergant, R. Maroofian, R. Zhao, M. Alfadhel, M. Nashabat, M. T. AlRifai, W. Eyaid, A. Alswaid, C. Beetz, Y. Qin, T. Zhu, Q. Tian, L. Xia, H. Wu, L. Shen, S. Dong, X. Yang, C. Liu, L. Ma, Q. Zhang, R. Khan, A. A. Shah, J. Guo, B. Tang, L. Leonardis, K. Writzl, B. Peterlin, H. Guo, S. Malik, K. Xia, Z. Hu, 2021 Akap2 Identified as a Novel Gene Mutated in a Chinese Family with Adolescent Idiopathic Scoliosis., W. Li, Y. Li, L. Zhang, H. Guo, D. Tian, Y. Peng, Y. Zheng, Y. Dai, K. Xia, X. Lan, B. Wang, Z. Hu, 2016 Mutations of P4ha2 Encoding Prolyl 4-Hydroxylase 2 Are Associated with Nonsyndromic High Myopia., H. Guo, P. Tong, Y. Liu, L. Xia, T. Wang, Q. Tian, Y. Li, Y. Hu, Y. Zheng, X. Jin, Y. Li, W. Xiong, B. Tang, Y. Feng, J. Li, Q. Pan, Z. Hu, K. Xia, 2015 Common Genetic Variants on 1p13.2 Associate with Risk of Autism., K. Xia, H. Guo, Z. Hu, G. Xun, L. Zuo, Y. Peng, K. Wang, Y. He, Z. Xiong, L. Sun, Q. Pan, Z. Long, X. Zou, X. Li, W. Li, X. Xu, L. Lu, Y. Liu, Y. Hu, D. Tian, L. Long, J. Ou, L. Zhang, Y. Pan, J. Chen, H. Peng, Q. Liu, X. Luo, W. Su, L. Wu, D. Liang, H. Dai, X. Yan, Y. Feng, B. Tang, J. Li, Z. Miedzybrodzka, J. Xia, Z. Zhang, X. Zhang, D. St Clair, J. Zhao, F. Zhang, 2014 Slc39a5 Mutations Interfering with the Bmp/Tgf-Beta Pathway in Non-Syndromic High Myopia., H. Guo, X. Jin, T. Zhu, T. Wang, P. Tong, L. Tian, Y. Peng, L. Sun, A. Wan, J. Chen, Y. Liu, Y. Li, Q. Tian, L. Xia, L. Zhang, Y. Pan, L. Lu, Q. Liu, L. Shen, W. Xiong, J. Li, B. Tang, Y. Feng, X. Zhang, Z. Zhang, Q. Pan, Z. Hu, K. Xia, 2014 Loss-of-Function Mutations in Filaggrin Gene Associate with Psoriasis Vulgaris in Chinese Population., Z. Hu, Z. Xiong, X. Xu, F. Li, L. Lu, W. Li, J. Su, Y. Liu, D. Liu, Z. Xie, Y. Peng, Y. Kuang, L. Wu, J. Zhang, Q. Pan, B. Tang, X. Chen, K. Xia, 2012 A Novel Locus for Congenital Simple Microphthalmia Family Mapping to 17p12-Q12., Z. Hu, C. Yu, J. Li, Y. Wang, D. Liu, X. Xiang, W. Su, Q. Pan, L. Xie, K. Xia, 2011

Areas of Focus

儿童孤独症的遗传基础及机制研究
高度近视的遗传基础及机制研究

Publications

The autism risk gene CNTN4 modulates dendritic spine formation., R. Zhao, T. Zhu, Q. Liu, Q. Tian, M. Wang, J. Chen, D. Tong, B. Yu, H. Guo, K. Xia, Z. Qiu, Z. Hu, 2021
Slc39a5 Dysfunction Impairs Extracellular Matrix Synthesis in High Myopia Pathogenesis., S. Dong, Q. Tian, T. Zhu, K. Wang, G. Lei, Y. Liu, H. Xiong, L. Shen, M. Wang, R. Zhao, H. Wu, B. Li, Q. Zhang, Y. Yao, H. Guo, K. Xia, L. Xia, Z. Hu, 2021
Biallelic Loss-of-Function Variants in Nemf Cause Central Nervous System Impairment and Axonal Polyneuropathy., A. Ahmed, M. Wang, G. Bergant, R. Maroofian, R. Zhao, M. Alfadhel, M. Nashabat, M. T. AlRifai, W. Eyaid, A. Alswaid, C. Beetz, Y. Qin, T. Zhu, Q. Tian, L. Xia, H. Wu, L. Shen, S. Dong, X. Yang, C. Liu, L. Ma, Q. Zhang, R. Khan, A. A. Shah, J. Guo, B. Tang, L. Leonardis, K. Writzl, B. Peterlin, H. Guo, S. Malik, K. Xia, Z. Hu, 2021
Akap2 Identified as a Novel Gene Mutated in a Chinese Family with Adolescent Idiopathic Scoliosis., W. Li, Y. Li, L. Zhang, H. Guo, D. Tian, Y. Peng, Y. Zheng, Y. Dai, K. Xia, X. Lan, B. Wang, Z. Hu, 2016
Mutations of P4ha2 Encoding Prolyl 4-Hydroxylase 2 Are Associated with Nonsyndromic High Myopia., H. Guo, P. Tong, Y. Liu, L. Xia, T. Wang, Q. Tian, Y. Li, Y. Hu, Y. Zheng, X. Jin, Y. Li, W. Xiong, B. Tang, Y. Feng, J. Li, Q. Pan, Z. Hu, K. Xia, 2015
Common Genetic Variants on 1p13.2 Associate with Risk of Autism., K. Xia, H. Guo, Z. Hu, G. Xun, L. Zuo, Y. Peng, K. Wang, Y. He, Z. Xiong, L. Sun, Q. Pan, Z. Long, X. Zou, X. Li, W. Li, X. Xu, L. Lu, Y. Liu, Y. Hu, D. Tian, L. Long, J. Ou, L. Zhang, Y. Pan, J. Chen, H. Peng, Q. Liu, X. Luo, W. Su, L. Wu, D. Liang, H. Dai, X. Yan, Y. Feng, B. Tang, J. Li, Z. Miedzybrodzka, J. Xia, Z. Zhang, X. Zhang, D. St Clair, J. Zhao, F. Zhang, 2014
Slc39a5 Mutations Interfering with the Bmp/Tgf-Beta Pathway in Non-Syndromic High Myopia., H. Guo, X. Jin, T. Zhu, T. Wang, P. Tong, L. Tian, Y. Peng, L. Sun, A. Wan, J. Chen, Y. Liu, Y. Li, Q. Tian, L. Xia, L. Zhang, Y. Pan, L. Lu, Q. Liu, L. Shen, W. Xiong, J. Li, B. Tang, Y. Feng, X. Zhang, Z. Zhang, Q. Pan, Z. Hu, K. Xia, 2014
Loss-of-Function Mutations in Filaggrin Gene Associate with Psoriasis Vulgaris in Chinese Population., Z. Hu, Z. Xiong, X. Xu, F. Li, L. Lu, W. Li, J. Su, Y. Liu, D. Liu, Z. Xie, Y. Peng, Y. Kuang, L. Wu, J. Zhang, Q. Pan, B. Tang, X. Chen, K. Xia, 2012
A Novel Locus for Congenital Simple Microphthalmia Family Mapping to 17p12-Q12., Z. Hu, C. Yu, J. Li, Y. Wang, D. Liu, X. Xiang, W. Su, Q. Pan, L. Xie, K. Xia, 2011

孤独症遗传学病因学细胞模型动物模型高通量测序外显子组捕获基因鉴定高度近视生物分子路径

蒋颖 - 同济大学

马龙 - 中南大学

王擎 - 华中科技大学

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