Author

Julie M. Schultz

National Institutes of Health

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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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

Thomas B. FriedmaniD· 2 shared Andrew J. GriffithiD· 1 shared Arnaud P. J. GieseiD· 1 shared Brittany N. Whitley· 1 shared Carmen C. BreweriD· 1 shared Connor HilliD· 1 shared Elizabeth A. H. WilsoniD· 1 shared Elizabeth J. Thomason· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersNeuroscience

Thomas B. FriedmanORCID

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Author profile →

2 papers

Recent·Most cited

Potential therapy for progressive vision loss due to PCDH15-associated Usher syndrome developed in an orthologous Usher mouse

Saumil Sethna, Wadih M. Zein, Sehar Riaz, Arnaud P. J. Giese, Julie M. Schultz, Todd E Duncan, Robert B. Hufnagel, Carmen C. Brewer, Andrew J. Griffith, T. Michael Redmond, Saima Riazuddin, Thomas B. Friedman, Zubair M. Ahmed

The paper describes a potential therapy for PCDH15-associated Usher syndrome using exogenous retinoids in a mouse model, showing improved ERG amplitudes.

bioRxiv · Jun 8, 2021 · PreprintNeuroscience

Noncoding microdeletion in mouse Hgf disrupts neural crest migration into the stria vascularis, reduces the endocochlear potential and suggests the neuropathology for human nonsyndromic deafness DFNB39

Robert J. Morell, Rafal T. Olszewski, Risa Tona, Samuel Leitess, Talah T. Wafa, Ian Taukulis, Julie M. Schultz, Elizabeth J. Thomason, Kerianne Richards, Brittany N. Whitley, Connor Hill, Thomas L. Saunders, Matthew F. Starost, Tracy S. Fitzgerald, Elizabeth A. H. Wilson, , Michael Hoa

This paper identifies a noncoding 10bp deletion in Hgf in mice that causes hearing loss by disrupting neural crest migration into the stria vascularis and reducing the endocochlear potential, mirroring human DFNB39 deafness.

Journal of Neuroscience · Mar 9, 2020Peer-reviewedGenetics