Author

Nan Li

BGI Group (China)ORCID 0000-0002-8248-9027Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Nan Li10 papers · Westlake University

Biology Disciplines

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Biophysics· 1 Developmental Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Baohua Niu· 1 shared C Yang· 1 shared Chengting ZhangiD· 1 shared Chi ZhangiD· 1 shared Gaohui ShiiD· 1 shared Gaozhi P MoiD· 1 shared Ge YangiD· 1 shared Genlin Liu· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperDevelopmental Biology

Baohua Niu

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3 papers

Recent·Most cited

BiophysicsbioRxivPreprintJun 18, 2026

Buffered sweat microfluidics with AI-enabled translation for clinically actionable blood urea estimation and renal risk stratification

Jiahao Zhang, Zhengquan Shen, Ming Xu…·Yunlong Zhao

This paper develops a wearable microfluidic patch with AI to estimate blood urea from sweat, enabling non-invasive renal monitoring with high accuracy.

DOI 10.64898/2026.06.17.732831

𝕏 PostBluesky

Developmental BiologyCell ResearchPeer-reviewedJul 17, 2023

Dissecting peri-implantation development using cultured human embryos and embryo-like assembloids

Zongyong Ai, Baohua Niu, Yu Yin…·Tianqing Li

The paper creates a cell atlas of early human peri-implantation lineages and develops an embryo-like assembloid to study lineage development and signaling mechanisms.

108 citationstop 1%

humanbulk RNA-seq

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Genetic & Genomic MedicinemedRxivPreprintJun 28, 2023

Unraveling the Molecular Landscape of Congenital Pseudoarthrosis of the Tibia: Insights from a Comprehensive Analysis of 162 Probands

Guanghui Zhu, Nan Li, Zheng Yu…·Haibo Mei

This study identifies rare LoF variations in key pathways associated with CPT, explaining ~39.6% of cases and highlighting genetic mechanisms underlying the disease.

DOI 10.1101/2023.06.28.23292011

humanwhole-exome sequencing

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