Author

Xinyao Zhou

Tongji UniversityORCID 0000-0002-0544-2276Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aiping MaoiD· 1 shared Fanwei ZengiD· 1 shared Fengxia LiuiD· 1 shared Fengyu Wu· 1 shared Gang ZouiD· 1 shared Gang ZouiD· 1 shared Jia ZhouiD· 1 shared Jian WangiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aiping MaoORCID

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2 papers

Recent·Most cited

Berrylyzer-an Efficient, Traceable, and Lightweight Intelligent Agentic System for Prenatal Genetic Diagnosis

Meng Meng, Ling Liu, Qianqian Du, Xinyao Zhou, Yuan Tian, Kuan Sun, Naiqi Li, Pinggui Zhang, Xianyi Lian, Ning Fan, Na Zhu, Shujing Li, Aiping Mao, Yuezhen Li, Gang Zou

Berrylyzer is a variant prioritization system for prenatal genetic diagnosis that outperforms existing tools in ranking diagnostic variants and recall rates.

medRxiv · Apr 4, 2026 · PreprintGenetic & Genomic Medicine

Comprehensive genome sequencing analysis as a promising option in the prenatal diagnosis of fetal structural anomalies: a prospective study.

Jia Zhou, Ziying Yang, Jun You Sun, Lipei Liu, Xinyao Zhou, Fengxia Liu, Ya Xing, Shuge Cui, Shiyi Xiong, Xiaoyu Liu, Yingjun Yang, Xiuxiu Wei, Gang Zou, Zhonghua Wang, Xing Wei, , Luming Sun

This study evaluates genome sequencing as a first-line prenatal diagnostic tool, finding it more comprehensive than CMA plus exome sequencing in detecting genetic anomalies and nongenetic factors.

bioRxiv · Aug 22, 2020 · PreprintGenomics