Author

Martin L. Katz

University of MissouriORCID 0000-0002-2582-9187Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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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 Garrett BullockiD· 1 shared Inès BarthélémyiD· 1 shared Kaspar MatiasekiD· 1 shared

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2025-2025 · peak 1/yr

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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

GeneticsbioRxivPreprintOct 16, 2025

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

Lucie Chevallier, Garrett Bullock, Thibaut Troupel…·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.

DOI 10.1101/2025.10.16.682890

whole-genome sequencingstatistical model

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