Qiuju Wang (Jing Guan)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 8

Top Topics

Pluripotent Stem Cells

Psychometric Properties

Top Venues

Journal of neurogenetics

BMC medical genetics

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

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

Publications

Qiuju Wang, Xiaonan Wu, Jiao Zhang, Jin Li, Hongyang Wang, Qiuju Wang
Global research landscape on the contribution of de novo mutations to human genetic diseases over the past 20 years: bibliometric analysis. Journal of neurogenetics 38 (1) (2024)
Qiuju Wang, Xiaonan Wu, Jiao Zhang, Jin Li, Hongyang Wang, Qiuju Wang
Global research landscape on the contribution of de novo mutations to human genetic diseases over the past 20 years: bibliometric analysis. Journal of neurogenetics (2024)
Qiuju Wang, Hongyang Wang, Lan Lan, Yusen Wu, Guohui Chen, Cui Zhao, Dayong Wang, Qiuju Wang
Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss. Molecular genetics & genomic medicine 8 (8) (2020)
Hongyang Wang, Li Wang, Ju Yang, Linwei Yin, Lan Lan, Jin Li, Qiujing Zhang, Dayong Wang, Jing Guan, Qiuju Wang
Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy. BMC medical genetics 20 (1) (2019)
Jing Zhang, Jing Guan, Hongyang Wang, Linwei Yin, Dayong Wang, Lidong Zhao, Huifang Zhou, Qiuju Wang
Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss. BMC medical genetics 20 (1) (2019)
Hongyang Wang, Qiuju Wang, Liping Guan, Ju Yang, Kaiwen Wu, Qiongfen Lin, Wenping Xiong, Lan Lan, Cui Zhao, Linyi Xie, Lan Yu, null Dan Bing, Lidong Zhao, Dayong Wang, Qiuju Wang
Further evidence for "gain-of-function" mechanism of DFNA5 related hearing loss. Scientific reports 8 (1) (2018)
Jing Guan, Hongyang Wang, Lan Lan, Li Wang, Ju Yang, Linyi Xie, Zifang Yin, Wenping Xiong, Lidong Zhao, Dayong Wang, Qiuju Wang
Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss. American journal of medical genetics. Part A 176 (1) (2017)
Qiuju Wang, Dayong Wang, Wenjian Cao, Yali Zhao, Renqian Du, Hu Yuan, Qiong Liu, Lan Lan, Liang Zong, Ju Yang, Zifang Yin, Bing Han, Feng Zhang, Qiuju Wang
SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans. Journal of human genetics 61 (11) (2016)