Author

Bradley A. Schulte

Medical University of South Carolina

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· 2

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Judy R. DubnoiD· 2 shared Karen P. SteeliD· 2 shared Morag A. LewisiD· 2 shared Claire Joanne StevesiD· 1 shared Frances M. K. WilliamsiD· 1 shared Jennifer Schulte· 1 shared Kenneth I. VadeniD· 1 shared Lois J. MatthewsiD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Judy R. DubnoORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss

Morag A. Lewis, Jennifer Schulte, Lois J. Matthews, Kenneth I. Vaden, Claire Joanne Steves, Frances M. K. Williams, Bradley A. Schulte, Judy R. Dubno, Karen P. Steel

PLoS Genetics · Nov 27, 2023Peer-reviewedGenetic & Genomic Medicine

Investigating the Characteristics of Genes and Variants Associated with Self-Reported Hearing Difficulty in Older Adults in the UK Biobank

Morag A. Lewis, Bradley A. Schulte, Judy R. Dubno, Karen P. Steel

This study identifies genes and variants associated with self-reported hearing difficulty in older adults using UK Biobank exome sequencing data, finding that both common and rare variants contribute to age-related hearing loss, with sex-specific differences.

BMC Biology · Jun 27, 2022Peer-reviewedGenetic & Genomic Medicine