Author

Yefeng Yang

McGill UniversityPrimary ORCID profile (0000-0002-8610-4016 · 2 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Yefeng YangiD2 papers · UNSW Sydney

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Chen‐Yang SuiD· 2 shared Hsuan Megan TsaoiD· 2 shared Leighton Smith· 2 shared Masashi HasebeiD· 2 shared Satoshi YoshijiiD· 2 shared Tianyuan LuiD· 2 shared Adriaan van der GraafiD· 1 shared Arthur Richard· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Chen‐Yang SuORCID

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2 papers

Recent·Most cited

Genomic atlas of cardiac and adiposity imaging phenotypes

Hui‐Mei Tsao, Leighton Smith, Arthur Richard, Urvashi Singh, Masashi Hasebe, Chen‐Yang Su, Yefeng Yang, Hongyu Xiao, Trang Nguyen, Patrick Smadbeck, Jason A. Flannick, Tianyuan Lu, Satoshi Yoshiji

The paper constructs a genomic atlas of cardiac and adiposity imaging phenotypes using whole-genome sequencing data from UK Biobank, identifying genetic associations and polygenic scores linked to cardiometabolic diseases.

medRxiv · Sep 30, 2026 · PreprintGenetic & Genomic Medicine

Systematic variant-to-gene mapping highlights TGFB2 and VEGFA as adipokine-coding genes with non-obese, insulin-resistance-like characteristics and distinct disease risks

Chen‐Yang Su, Masashi Hasebe, Adriaan van der Graaf, Yefeng Yang, Hsuan Megan Tsao, Leighton Smith, Guillaume Butler‐Laporte, Sirui Zhou, Wenmin Zhang, Tianyuan Lu, Satoshi Yoshiji

The paper maps adipokine-associated variants to effector genes across 1,669 traits, identifying TGFB2 and VEGFA as linked to insulin resistance and distinct disease risks.

medRxiv · May 4, 2026 · PreprintGenetic & Genomic Medicine