Kevin Ta Booth

18PUBLICATIONS
81CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Anthropological geneticsNeurology and neuromuscular diseasesCell and nuclear divisionNeural engineering
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (18)

|Apr 14, 2026
The AudioGene Translational Dashboard for Diagnosing Autosomal Dominant Nonsyndromic Hearing Loss: Phenotypic Data Visualization and Analysis Study.

Benjamin DeSollar, Nathan Schaefer, Daniel Walls

|Jan 14, 2026
Novel RNF113A Variant Underlying X-Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother.

Rachel Rabin, Kevin T A Booth, Shawn E Cowper

|Sep 29, 2025
Investigation of GSDME results in the identification of the first pathogenic synonymous variants and genotype-phenotype correlations.

Joseph J Chin, W Daniel Walls, Kai Wang

|Aug 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders.

Sara M Fielder, Marisa W Friederich, Daniella H Hock

|Feb 26, 2025
A Novel Candidate Gene <i>MACF1</i> is Associated with Autosomal Dominant Non-syndromic Hearing Loss in an Iranian Family.

Niloofar Bazazzadegan, Mojgan Babanejad, Susan Banihashemi

|Jan 07, 2025
Cell-specific delivery of GJB2 restores auditory function in mouse models of DFNB1 deafness and mediates appropriate expression in NHP cochlea.

Maryna V Ivanchenko, Kevin T A Booth, K Domenica Karavitaki

Pageof 3

Frequent Collaborators

9 joint publications

Richard Jh Smith

8 joint publications

Hela Azaiez

4 joint publications

Kimia Kahrizi

4 joint publications

Hossein Najmabadi