Author

Jennifer 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· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

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

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Bradley A. Schulte

Mutual co-authors in cluster

Author profile →

1 paper

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