Author

Garrett Bullock

University of MissouriORCID 0000-0002-9231-8758Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ambre CourtiniD· 1 shared Caroline Dufaure de CitresiD· 1 shared Catherine EscriouiD· 1 shared Dennis P O’BrieniD· 1 shared Frank SteffeniD· 1 shared Inès BarthélémyiD· 1 shared Kaspar MatiasekiD· 1 shared Laurent TiretiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Ambre CourtinORCID

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1 paper

Recent·Most cited

A missense variant in PAOX in American Staffordshire Terriers with juvenile-onset polyneuropathy

Lucie Chevallier, Garrett Bullock, Thibaut Troupel, Nicolas Blanchard‐Gutton, Inès Barthélémy, Kaspar Matiasek, Frank Steffen, Ambre Courtin, Liz Hansen, Matthias Christen, Vidhya Jagannathan, Caroline Dufaure de Citres, Marion Signoret, Catherine Escriou, Marie Abitbol, , Martin L. Katz

This paper identifies a missense variant in the PAOX gene as the cause of juvenile-onset polyneuropathy in American Staffordshire Terriers, highlighting its potential as a model for human Charcot-Marie-Tooth disease.

bioRxiv · Oct 16, 2025 · PreprintGenetics