Author

Jing Zhou

BGI Group (China)ORCID 0000-0001-6601-4446Unclaimed ORCID profile · follow to get notified of new preprints

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Jing Zhou3 papers · Dian Diagnostics (China)

Biology Disciplines

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Genetic & Genomic Medicine· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

Haisheng Yan· 2 shared Jian GuoiD· 2 shared Jingyu YeiD· 2 shared Nianji Zhan· 2 shared Shida ZhuiD· 2 shared Tongda Zhang· 2 shared Zhenzhen YiniD· 2 shared A‐Bin YouiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Haisheng Yan

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3 papers

Recent·Most cited

Molecular BiologybioRxivPreprintJul 20, 2025

No phenotypes in Ttc22 knockout mice

Jiaoyang Liu, Liankun Gu, A‐Bin You…·Dajun Deng

This paper investigates the effects of Ttc22 knockout in mice and finds no significant phenotypes in development, fertility, or colon cancer induction.

DOI 10.1101/2025.07.20.665798

mouseproteomics

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Genetic & Genomic MedicineBrainPeer-reviewedJun 17, 2021

Clinical and molecular diagnostic study of 320 Chinese children with epilepsy by Genome Sequencing

Dongfang Zou, Lin Wang, Jianxiang Liao…·Jian Guo

This study evaluates genome sequencing in 320 Chinese children with epilepsy, finding pathogenic variants in 38.13% and demonstrating its diagnostic and therapeutic value.

37 citationstop 4%

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintMar 4, 2020

Genome sequencing combining prenatal ultrasound in the evaluation of fetal CNS structural anomalies

Ying Yang, Sheng Zhao, Guoqiang Sun…·Xinlin Chen

This study evaluates genome sequencing for diagnosing fetal CNS structural anomalies, finding a 38.9% overall diagnostic yield and higher rates in specific malformations.

1 citation

humanwhole-genome sequencing

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