Author

Yu Deng

Guangzhou Women and Children Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

B Liu· 1 shared Chao LiiD· 1 shared Chunlin LiuiD· 1 shared Hanwang Zhang· 1 shared Hao HuiD· 1 shared Ling SuniD· 1 shared Min-Na Yin· 1 shared Na LiiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenomics

B Liu

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2 papers

Recent·Most cited

Whole-genome sequencing reveals variant associations with brain imaging phenotypes

B Liu, Yu Deng, Chao Li

This study uses whole-genome sequencing to identify genetic variants associated with brain imaging phenotypes, finding significant associations at both variant and gene levels.

bioRxiv · Jan 8, 2026 · PreprintGenomics

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