Richard Jh Smith

21PUBLICATIONS
87CO-AUTHORS
Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)Formal methods for softwareCardiology (incl. cardiovascular diseases)Medical devices
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Publications (21)

|Sep 30, 2026
The prevalence of protein misfolding as a mechanism for hereditary deafness.

|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

|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

|Jul 03, 2024
Force Field X: A computational microscope to study genetic variation and organic crystals using theory and experiment.

Rose A Gogal, Aaron J Nessler, Andrew C Thiel

|Jun 03, 2024
Developing Therapies for C3 Glomerulopathy: Report of the Kidney Health Initiative C3 Glomerulopathy Trial Endpoints Work Group.

Carla Nester, Dima A Decker, Matthias Meier

|Dec 27, 2022
Mutation-agnostic RNA interference with engineered replacement rescues Tmc1-related hearing loss.

Yoichiro Iwasa, Miles J Klimara, Hidekane Yoshimura

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Frequent Collaborators

9 joint publications

Kevin T Booth

8 joint publications

Hela Azaiez

4 joint publications

Kimia Kahrizi

4 joint publications

William D Walls