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
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
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
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
