Hela Azaiez

10PUBLICATIONS
67CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene mappingNeurogeneticsSensory systemsMicrobial taxonomy
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Publications (10)

|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

|Feb 22, 2023
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy.

Rabia Faridi, Rizwan Yousaf, Shoujun Gu

|Jan 26, 2021
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans.

Barbara Vona, Neda Mazaheri, Sheng-Jia Lin

|Jan 05, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing.

Yoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth

|Jun 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss.

Kevin T Booth, Amama Ghaffar, Muhammad Rashid

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Frequent Collaborators

8 joint publications

Kevin T Booth

8 joint publications

Richard Jh Smith

3 joint publications

Kimia Kahrizi

3 joint publications

Hossein Najmabadi