Author

Bryan Walters

University of Vermont

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Research Focus:cell-cell communication· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Adrian M. Sackheim· 1 shared Aleksandar RajkoviciD· 1 shared Amrita NagasuriiD· 1 shared Aryo Garakani· 1 shared Catherine Hypes· 1 shared Christina G. TiseiD· 1 shared Christopher Bidlack· 1 shared David K. StevensoniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperPhysiology

Adrian M. Sackheim

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2 papers

Recent·Most cited

Spatial uncoupling of endothelial calcium signaling from phosphatidylserine externalization in vascular injury

Olivia Fauver, Grant W. Hennig, Adrian M. Sackheim, Bryan Walters, Rachel Barba, Rushi Sonawane, Christopher Bidlack, Devdoot S. Majumdar, Mohamed Trebak, Mark T. Nelson, Kalev Freeman

This study shows that endothelial calcium signaling spreads widely during vascular injury, but phosphatidylserine externalization remains localized, revealing spatial uncoupling between calcium signaling and phospholipid scrambling.

bioRxiv · Oct 24, 2026 · PreprintPhysiology

The Human Intolerome: a curated database to prioritize genomic variants in stillbirth, pregnancy loss, and neonatal death

Svetlana A. Yatsenko, Amrita Nagasuri, Vishal Soman, Aryo Garakani, Mona Amin‐Beidokhti, Uma Chandran, Mahmoud Aarabi, Tomiko Oskotsky, Syed Hassan Bukhari, Catherine Hypes, Zhiping Gu, Ruth Monteiro, Sammi E. Smith, Bryan Walters, Michael P. Snyder, , Aleksandar Rajkovic

The paper introduces the Intolerome Database, a curated resource of genes essential for human viability, to help prioritize genomic variants in cases of stillbirth, pregnancy loss, and neonatal death.

Genetics in Medicine · Mar 3, 2026Peer-reviewedGenetic & Genomic Medicine