Zhengmao Hu

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Venues

Journal of medical genetics

BMC medical genomics

Journal of cellular and molecular medicine

Human molecular genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Xiaozhen Chen, Ping Tong, Ying Jiang, Zhe Cheng, Liyu Zang, Zhikuan Yang, Weizhong Lan, Kun Xia, Zhengmao Hu, Qi Tian
CCDC66 mutations are associated with high myopia through affected cell mitosis. Journal of medical genetics (2023)
Qi Tian, Ping Tong, Gong Chen, Meichun Deng, Tian'e Cai, Runyi Tian, Zimin Zhang, Kun Xia, Zhengmao Hu
GLRA2 gene mutations cause high myopia in humans and mice. Journal of medical genetics (2022)
Sida Huang, Lu Ma, Xuezhong Liu, Chufeng He, Jiada Li, Zhengmao Hu, Lu Jiang, Yalan Liu, Xianlin Liu, Yong Feng, Xinzhang Cai
A non-coding variant in 5' untranslated region drove up-regulation of Pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans. Human molecular genetics (2022)
Shanshan Dong, Qi Tian, Tengfei Zhu, Kangli Wang, Ganting Lei, Yanling Liu, Haofeng Xiong, Lu Shen, Meng Wang, Rongjuan Zhao, Huidan Wu, Bin Li, Qiumeng Zhang, Yujun Yao, Hui Guo, Kun Xia, Lu Xia, Zhengmao Hu
SLC39A5 dysfunction impairs extracellular matrix synthesis in high myopia pathogenesis. Journal of cellular and molecular medicine 25 (17) (2021)
Ashfaque Ahmed, Meng Wang, Rizwan Khan, Abid Ali Shah, Hui Guo, Sajid Malik, Kun Xia, Zhengmao Hu
A splice-site variant (c.3289-1G>T) in OTOF underlies profound hearing loss in a Pakistani kindred. BMC medical genomics 14 (1) (2021)
Ashfaque Ahmed, Meng Wang, Gaber Bergant, Reza Maroofian, Rongjuan Zhao, Majid Alfadhel, Marwan Nashabat, Muhammad Talal AlRifai, Wafaa Eyaid, Abdulrahman Alswaid, Christian Beetz, Yan Qin, Tengfei Zhu, Qi Tian, Lu Xia, Huidan Wu, Lu Shen, Shanshan Dong, Xinyi Yang, Cenying Liu, Linya Ma, Qiumeng Zhang, Rizwan Khan, Abid Ali Shah, Jifeng Guo, Beisha Tang, Lea Leonardis, Karin Writzl, Borut Peterlin, Hui Guo, Sajid Malik, Kun Xia, Zhengmao Hu
Biallelic loss-of-function variants in NEMF cause central nervous system impairment and axonal polyneuropathy. Human genetics 140 (4) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Zhengmao Hu