Author

Qian‐Ying Zhu

Guangzhou Women and Children Medical CenterORCID 0000-0002-7463-5290Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Hao HuiD· 2 shared Na LiiD· 2 shared Pei ZhouiD· 2 shared Ting XueiD· 2 shared Xiang FangiD· 2 shared Xiaofang PengiD· 2 shared Caihua Liao· 1 shared Changgeng PengiD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

Hao HuORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

In-depth analysis reveals complex molecular etiology of idiopathic cerebral palsy

Na Li, Pei Zhou, Hongmei Tang, Lu He, Xiang Fang, Jinxiang Zhao, Xin Wang, Yifei Qi, Chuanbo Sun, Yunting Lin, Fengying Qin, Miaomiao Yang, Zhan Zhang, Caihua Liao, Shuxin Zheng, , Hao Hu

This study identifies molecular risk factors and mechanisms in idiopathic cerebral palsy through clinical and molecular analysis of 120 families.

bioRxiv · Aug 17, 2020 · PreprintGenetics

Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters

Ling Sun, Xiang Fang, Zhiheng Chen, Hanwang Zhang, Zhan Zhang, Pei Zhou, Ting Xue, Xiaofang Peng, Qian‐Ying Zhu, Min-Na Yin, Chunlin Liu, Yu Deng, Hao Hu, Na Li

Human Mutation · Jul 11, 2019Peer-reviewedGenetics