Author

Xinyu Miao

McGill UniversityPrimary ORCID profile (0000-0001-6745-4734 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Xinyu MiaoiD1 paper · Soochow University

Biology Disciplines

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Bioinformatics· 1 Cell Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Organism:Drosophila· 1 Research Focus:host-pathogen & immune response· 1 Approach:machine learning (classical)· 1 Research Focus:software / tool· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Nazlı BaşakiD· 1 shared Abigail D. WilsoniD· 1 shared Albena JordanovaiD· 1 shared Alexander Martin RossoriD· 1 shared Ali CansuiD· 1 shared André Luiz Santos PessoaiD· 1 shared Andrea CorteseiD· 1 shared Annarita ScardamagliaiD· 1 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Nazlı BaşakORCID

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Author profile →

3 papers

Recent·Most cited

Platycodin D2 Targets Vimentin to Suppress Fibroblast-Myofibroblast Transition: A Novel Therapeutic Strategy Against Pulmonary Fibrosis

Xianshengjie Lang, Zheng Ma, Chuning Yao, Xinyu Miao, Yuchenyang Kao, Wenwen Wang, Shuangli Sun

This study identifies Platycodin D2 as a vimentin ligand that suppresses fibroblast-myofibroblast transition, offering a new therapeutic approach for pulmonary fibrosis.

bioRxiv · Nov 5, 2026 · PreprintCell Biology

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

Biallelic variants in ARHGAP19 cause a motor-predominant neuropathy with asymmetry and conduction slowing

Natalia Dominik, Stéphanie Efthymiou, Christopher J. Record, Xinyu Miao, Renee Lin, J. Parmar, Annarita Scardamaglia, Reza Maroofian, Gabriel Aughey, Abigail D. Wilson, Simon A. Lowe, Riccardo Curró, Ricardo Parolin Schnekenberg, Shahryar Alavi, Leif Leclaire, , Henry Houlden

The paper identifies biallelic variants in ARHGAP19 as a cause of motor-predominant neuropathy with conduction slowing in multiple families.

medRxiv · May 10, 2024 · PreprintGenetic & Genomic Medicine