Shelby Redfield
5PUBLICATIONS
12CO-AUTHORS
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Publications (5)
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|Apr 18, 2025
A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets.Shelby E Redfield, Stephanie A Mauriac, Gwenaëlle S Géléoc
|Mar 10, 2025
A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets.Shelby E Redfield, Stephanie A Mauriac, Gwenaëlle S Géléoc
|Mar 08, 2024
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss.Shelby E Redfield, Pedro De-la-Torre, Mina Zamani
|Oct 24, 2023
PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss.Shelby E Redfield, Pedro De-la-Torre, Mina Zamani
|Dec 14, 2022
Exome Sequencing Expands the Genetic Diagnostic Spectrum for Pediatric Hearing Loss.Julia Perry, Shelby Redfield, Andrea Oza
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Frequent Collaborators
5 joint publications
Eliot Shearer
2 joint publications
Pedro De-la-Torre
2 joint publications
Mina Zamani
2 joint publications
Sadaf Naz
2 joint publications
Artur A Indzhykulian
2 joint publications
Barbara Vona
2 joint publications
Margaret Kenna
2 joint publications
Stephanie A Mauriac
2 joint publications
Gwenaëlle S Géléoc
1 joint publications
Hongen Xu
