Chanjuan Hao
6PUBLICATIONS
20CO-AUTHORS
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Publications (6)
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|Nov 14, 2025
Targeted genetic screening for identifying carrier status and early-onset disease risks in Chinese newborns.Chanjuan Hao, Xuyun Hu, Ruolan Guo
|Oct 24, 2024
Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screening.Chanjuan Hao, Xuyun Hu, Ruolan Guo
|Aug 31, 2024
DVsc: An Automated Framework for Efficiently Detecting Viral Infection from Single-cell Transcriptomics Data.Fei Leng, Song Mei, Xiaolin Zhou
|Dec 01, 2023
Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine.Wenyan Zhang, Ziming Yao, Ruolan Guo
|Sep 30, 2021
Identification and functional analysis of novel SLC25A19 variants causing thiamine metabolism dysfunction syndrome 4.Yuanying Chen, Boliang Fang, Xuyun Hu
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