Author

Bo Yang

University of MichiganORCID 0000-0002-2158-9155Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Bo Yang4 papers · Cornell University

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Alejandro Ponce· 1 shared Anders Franco‐CerecedaiD· 1 shared Anders HamsteniD· 1 shared Andreas MartinssoniD· 1 shared Anna HelgadóttiriD· 1 shared Arnar GeirssoniD· 1 shared Chad M. BrummettiD· 1 shared Charles S. ChungiD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Alejandro Ponce

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2 papers

Recent·Most cited

A Marfan-Associated FBN1 Nonsense Mutation Mouse Model Reveals Adventitial Inflammation During Aneurysm Progression

Shichao Wu, Jiawei Zhao, Alejandro Ponce, Lucynda Pham, Daniel Xie, Donghong Ju, Shuping Yin, Francis Hernandez, Sean Jones, Clair Li, Charles S. Chung, Dragana Komnenov, Noreen F. Rossi, Dogukan Mizrak, Bo Yang, , Li Li

This paper develops a mouse model with a FBN1 nonsense mutation to study aneurysm progression, finding that adventitial inflammation contributes to aortic aneurysm rupture.

bioRxiv · Sep 23, 2025 · PreprintGenetics

Genome-wide analysis yields new loci associating with aortic valve stenosis

Anna Helgadóttir, Guðmar Þorleifsson, Sólveig Grétarsdóttir, Ólafur Andri Stefánsson, Vinicius Tragante, Rósa B. Þórólfsdóttir, Ingileif Jónsdóttir, Þorsteinn Björnsson, Valgerður Steinthórsdóttir, Niek Verweij, Jonas Bille Nielsen, Wei Zhou, Lasse Folkersen, Andreas Martinsson, Mahyar Heydarpour, , Kāri Stefánsson

This study identifies two new genetic loci associated with aortic valve stenosis through a large genome-wide association study.

Nature Communications · Mar 1, 2018Peer-reviewedGenetics