Author

Chuanyi Zhang

Regeneron (United States)ORCID 0000-0001-6014-7993Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:database / resource· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Adam E. LockeiD· 2 shared Aris BarasiD· 2 shared Gonçalo R. AbecasisiD· 2 shared Jaime Berumen-CamposiD· 2 shared Jason TorresiD· 2 shared Jonas BovijniD· 2 shared Jonathan MarchiniiD· 2 shared Joshua BackmaniD· 2 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adam E. LockeORCID

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2 papers

Recent·Most cited

Rare protein-coding variation and the genetic architecture of height in >1.4 million individuals

Jack A. Kosmicki, Liron Ganel, Kyoko Watanabe, Tyler Joseph, Sheila M. Gaynor, Michael D. Kessler, Joshua Backman, Joelle S. Mbatchou, Andrey Ziyatdinov, David Blair, Jonas Bovijn, Niek Verweij, Kathie Sun, Chuanyi Zhang, Suganthi Balasubramanian, , Adam E. Locke

This study identifies 207 height-associated genes using rare protein-altering variants from over 1.4 million individuals, showing large effect sizes and overlap with Mendelian height syndromes.

medRxiv · Jun 24, 2026 · PreprintGenetic & Genomic Medicine

A deep catalog of protein-coding variation in 985,830 individuals

Kathie Sun, Xiaodong Bai, Siying Chen, Suying Bao, Manav Kapoor, Chuanyi Zhang, Joshua Backman, Tyler Joseph, Evan K. Maxwell, George Mitra, Alexander Gorovits, Adam J. Mansfield, Boris Boutkov, Sujit Gokhale, Lukas Habegger, , Suganthi Balasubramanian

This paper presents the largest catalog of human protein-coding variation from 985,830 individuals, identifying rare variants and their functional implications for precision medicine.

bioRxiv · May 9, 2023 · PreprintGenetics