Chunqiu Wu
6 Papers
7 Citations
Chunqiu Wu is an academic researcher. The author has contributed to research in topics: Compound heterozygosity & Mutation (genetic algorithm). The author has an hindex of 2, co-authored 5 publications.
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Papers
Different Circulation Pattern of Multiple Respiratory Viruses in Southern China During the COVID-19 Pandemic
Zhiqi Zeng,Wenda Guan,Yong Liu,Zhengshi Lin,Wenhua Liang,Jingyi Liang,Bingqian Chen,Tong Wu,Yutao Wang,Chunguang Yang,Qiubao Wu,Zhitong Mai,Jin-min Zhou,Jun Bo Zhou,Zhoulang Wang,Zhijie Lin,Chun-xiang Hu,Chunqiu Wu,Pengyuan Zhu,Canxiong Chen,Nanshan Zhong,Eric H. Y. Lau,C. Hon,Yaoming Liang,Zifeng Yang,Jianxing He +25 more
TL;DR: It is found that while the overall activity of respiratory viruses was lower during the period with stringent NPIs, virus activity rebounded shortly after the NPIs were relaxed and social activities resumed, showing that NPIs against COVID-19 have different impacts on respiratory viruses.
16
A novel variant in the CDH23 gene is associated with non-syndromic hearing loss in a Chinese family.
Yuan Liang,Kangwei Wang,Qi Peng,Pengyuan Zhu,Chunqiu Wu,Chunbao Rao,Jiang Chang,Siping Li,Xiaomei Lu +8 more
TL;DR: This study demonstrates that the novel variant c.4567A > G in the CDH23 gene is the main cause of binaural profound sensorineural hearing loss (DFNB12) without retinitis pigmentosa in the proband.
5
A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family
TL;DR: This study demonstrates that the novel mutation c.2239_2240delAG in the MYO7A gene is the main cause of USH1 in the proband, and expands the mutational spectrum of MYO 7A and provides a foundation for further investigations elucidating the MYo7A-related mechanisms of USh1.
2
A targeted gene capture next-generation sequencing panel for genetic screening of newborns.
Qi Peng,Guojun Liu,Pengyuan Zhu,Chunqiu Wu,Xiaoguang He,Wenrui Li,Chunbao Rao,Siping Li,Xiaomei Lu +8 more
TL;DR: A dried blood spot (DBS)-based targeted NGS panel for efficient genetic screening of a wide variety of genetic diseases in newborns was developed and evaluated and showed 100% consistency in detecting 8 pathogenic insertion/deletion (indels) variants.
2
A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct.
Yuan Liang,Qi Peng,Kangwei Wang,Pengyuan Zhu,Chunqiu Wu,Chunbao Rao,Jiang Chang,Siping Li,Xiaomei Lu +8 more
TL;DR: This study demonstrates that the novel mutation c.2110 G > C (p.Glu704Gln) in compound heterozygosity with c.1673 A’n558Ile in the SLC26A4 gene corresponds to the EVA in this family of Han Chinese family with enlarged vestibular aqueduct syndrome.