Author

Cheng Chen

Hubei Provincial Women and Children's HospitalORCID 0000-0002-3677-7992Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Cheng Chen4 papers · BGI Group (China)

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:dimensionality reduction· 1 Assay:imaging· 1 Organism:mouse· 1 Organism:non-human primate· 1

Frequent Co-Authors

Bin Rao· 1 shared Chet C. SherwoodiD· 1 shared Deying LiiD· 1 shared Fang CheniD· 1 shared Guoqiang SuniD· 1 shared Haisheng Yan· 1 shared Hui HuangiD· 1 shared Jian GuoiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Bin Rao

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2 papers

Recent·Most cited

Cross-Species Cortical Geometry Reveals Conserved Gradients Across Primates and Human-Specific Expansion

Yifan Wei, Yufan Wang, Tingwei Wei, Xiaoting Lu, Deying Li, Chet C. Sherwood, Yu Zhang, Cheng Chen, Tianzi Jiang, Lingzhong Fan, Luqi Cheng

The paper develops a cross-species cortical alignment framework to analyze structural connectivity and cortical expansion across primates, revealing conserved geometric patterns and human-specific expansions.

bioRxiv · Nov 28, 2025 · PreprintNeuroscience

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

Ying Yang, Sheng Zhao, Guoqiang Sun, Fang Chen, Tongda Zhang, Jieping Song, Wenzhong Yang, Lin Wang, Nianji Zhan, Xiaohong Helena Yang, Xia Zhu, Bin Rao, Zhenzhen Yin, Jing Zhou, Haisheng Yan, , 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.

medRxiv · Mar 4, 2020 · PreprintGenetic & Genomic Medicine