Eliot Shearer

14PUBLICATIONS
22CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Infant and child healthEnglish languageGene mapping
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (14)

|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

|Jan 31, 2025
Predictors of Posttransplant Lymphoproliferative Disease in Pediatric Patients.

Brett Campbell, Alexa J Kacin, JoAnn Morey

|Jun 10, 2024
High prevalence of syndromic hearing loss in Mexican children undergoing cochlear implantation.

Monica Rodriguez-Valero, Adrian Pastolero, Shelby Redfield

|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

Pageof 3