Author

Wei Ge

ShanghaiTech University

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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Bioinformatics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:machine learning (classical)· 1 Research Focus:software / tool· 1 Approach:statistical model· 1

Frequent Co-Authors

Bingjie ZhangiD· 1 shared Boxun LuiD· 1 shared Chunyan HouiD· 1 shared Guang YangiD· 1 shared Huilan WangiD· 1 shared Jianbo Deng· 1 shared Jie YuiD· 1 shared Jingwen Li· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

Bingjie ZhangORCID

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2 papers

Recent·Most cited

A Novel Glycoproteomics Platform for High-Throughput Identification of Disease-Associated Glycoforms

Shengye Wen, Yu Gao, Xinyu Miao, Jianbo Deng, Yufeng Zhou, Wei Ge, Siyue Bo, Wenqi Zhang, Rumeng Zhang, Chunyan Hou, Junfeng Ma, Junhong Jiang, Shuang Yang

The paper introduces GDAS, a high-throughput glycoproteomics platform that identifies disease-specific glycoforms using mass spectrometry data and machine learning.

bioRxiv · Mar 9, 2026 · PreprintBioinformatics

Post-translational modifications orchestrate the intrinsic signaling bias of orphan receptor GPR52

Bingjie Zhang, Wei Ge, Mengna Ma, Shanshan Li, Jie Yu, Guang Yang, Huilan Wang, Jingwen Li, Qingrun Li, Rong Zeng, Boxun Lu, Wenqing Shui

This study identifies how N-glycosylation and phosphorylation in specific motifs of GPR52 differentially regulate its signaling bias and cellular function.

Nature Chemical Biology · Mar 14, 2025Peer-reviewedCell Biology