Qiuju Wang
7PUBLICATIONS
6CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (7)
Sort by Publication Date:
|Apr 22, 2024
Global research landscape on the contribution of de novo mutations to human genetic diseases over the past 20 years: bibliometric analysis.Jing Guan, Xiaonan Wu, Jiao Zhang
|Jun 23, 2020
Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss.Jing Guan, Hongyang Wang, Lan Lan
|Apr 07, 2019
Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss.Jing Zhang, Jing Guan, Hongyang Wang
|Jan 13, 2019
Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy.Hongyang Wang, Li Wang, Ju Yang
|Jun 01, 2018
Further evidence for "gain-of-function" mechanism of DFNA5 related hearing loss.Hongyang Wang, Jing Guan, Liping Guan
|Oct 20, 2017
Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss.Jing Guan, Hongyang Wang, Lan Lan
Pageof 2
