Author

Michael J. Schnieders

University of IowaORCID 0000-0003-1260-4592Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:Bayesian inference· 1 Assay:DNA methylation· 1 Organism:human· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Arthur Duston OdelliD· 1 shared Brian Hong· 1 shared Chloe Ovel· 1 shared Diana L. KolbeiD· 1 shared Genevieve M. Cox· 1 shared Héla AzaieziD· 1 shared Katherine McCormick· 1 shared Richard J. SmithiD· 1 shared

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2026-2026 · peak 1/yr

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1 shared paperGenetics

Arthur Duston OdellORCID

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1 paper

Recent·Most cited

GeneticsPLoS GeneticsPeer-reviewedSep 30, 2026

The prevalence of protein misfolding as a mechanism for hereditary deafness

Rose A. Gogal, Genevieve M. Cox, Diana L. Kolbe…·Michael J. Schnieders

The paper evaluates computational frameworks to prioritize pathogenic variants in deafness-associated genes, identifying 28,866 VUSs with high pathogenicity probability and improving diagnoses for 12 patients.

DOI 10.1371/journal.pgen.1012085

humanDNA methylation

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