Professor | Zhengmao Hu | Asia Growth Partners

Name	Zhengmao Hu
Contact Information	huzhengmao@sklmg.edu.cn
Language ability	Chinese, English
Province	Hunan

Name

Zhengmao Hu

Contact Information

huzhengmao@sklmg.edu.cn

Language ability

Chinese, English

Province

Hunan

University/Lab Affiliation and Title	Central South University
Faculty	Life Sciences
Academic Background & Achievements	2004/09-2007/07 Central South University/National Key Laboratory of Medical Genetics, PhD in Genetics 2001/09-2004/07 Central South University/National Key Laboratory of Medical Genetics, Master's in Genetics 1990/09-1994/07 Hunan Normal University, Department of Biology, Bachelor's in Biology
Work Experience	2019/01-Present - Central South University, School of Life Sciences, Vice Dean 2016/10-Present - Central South University/Medical Genetics Research Center, Researcher 2012/12-2013/12 - University of Illinois at Chicago, Visiting Scholar 2010/10-2016/09 - Central South University/National Key Laboratory of Medical Genetics, Associate Researcher 2007/07-2010/09 - Central South University, Assistant Researcher 1994/07-2001/08 - Hunan Edible Mushroom Research Institute, Intern Researcher/Assistant Researcher

University/Lab Affiliation and Title

Central South University

Faculty

Life Sciences

Academic Background & Achievements

2004/09-2007/07 Central South University/National Key Laboratory of Medical Genetics, PhD in Genetics
2001/09-2004/07 Central South University/National Key Laboratory of Medical Genetics, Master's in Genetics
1990/09-1994/07 Hunan Normal University, Department of Biology, Bachelor's in Biology

Work Experience

2019/01-Present - Central South University, School of Life Sciences, Vice Dean
2016/10-Present - Central South University/Medical Genetics Research Center, Researcher
2012/12-2013/12 - University of Illinois at Chicago, Visiting Scholar
2010/10-2016/09 - Central South University/National Key Laboratory of Medical Genetics, Associate Researcher
2007/07-2010/09 - Central South University, Assistant Researcher
1994/07-2001/08 - Hunan Edible Mushroom Research Institute, Intern Researcher/Assistant Researcher

Areas of Focus	Genetic basis and mechanisms of childhood autism Genetic basis and mechanisms of high myopia
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

Genetic basis and mechanisms of childhood autism
Genetic basis and mechanisms of high myopia

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

Autism Genetics Pathogenesis Cell Models Animal Models High-Throughput Sequencing Exome Capture Gene Identification High Myopia Biomolecular Pathways

Ying Jiang - Tongji University

Ma Long - Central South University

Chen Fuxue - Shanghai University

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