Chanjuan Hao

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 3

Top Topics

Decision Making

Top Venues

Orphanet journal of rare diseases

Genomics, proteomics & bioinformatics

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

Publications

Fei Leng, Song Mei, Xiaolin Zhou, Xuanshi Liu, Yefeng Yuan, Xiaochen Bo, Chongyi Hao, Ruolan Guo, Chanjuan Hao, Wei Li, Peng Zhang
DVsc: An Automated Framework for Efficiently Detecting Viral Infection from Single-cell Transcriptomics Data. Genomics, proteomics & bioinformatics 22 (2) (2024)
Wenyan Zhang, Ziming Yao, Ruolan Guo, Jun Cao, Wei Li, Chanjuan Hao, Xuejun Zhang
Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine. Orphanet journal of rare diseases 18 (1) (2023)
Yuanying Chen, Boliang Fang, Xuyun Hu, Ruolan Guo, Jun Guo, Kenan Fang, Jingwen Ni, Wei Li, Suyun Qian, Chanjuan Hao
Identification and functional analysis of novel SLC25A19 variants causing thiamine metabolism dysfunction syndrome 4. Orphanet journal of rare diseases 16 (1) (2021)