Abdelaziz Tlili

13PUBLICATIONS
26CO-AUTHORS
GenomicsMolecular targetsPredictive and prognostic markersNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (13)

|Jun 12, 2026
Comprehensive Insights into Perrault Syndrome: Genetic Diversity and Clinical Implications.

|Apr 28, 2026
LNA GapmeR silencing of KRAS G12V impairs growth and function in SW480 cells.

|May 14, 2025
Analysis of Genotype and Expression of FTO and ALKBH5 in a MENA-Region Renal Cell Carcinoma Cohort.

Muna Abdalla Alhammadi, Burcu Yener Ilce, Poorna Manasa Bhamidimarri

|Nov 27, 2024
Segregation of Trans Mutations in the CDH23 Gene in an Emirati Family with Sensorineural Hearing Loss.

Mariam Alsebeyi, Abdullah Al Mutery, Mohammad Tehsil Gul

|Nov 09, 2024
Identification of Genes Associated with Familial Focal Segmental Glomerulosclerosis Through Transcriptomics and In Silico Analysis, Including RPL27, TUBB6, and PFDN5.

Anfal Hussain Mahmoud, Reem Sami Alhamidi, Burcu Yener Ilce

|May 25, 2024
The Segregation of p.Arg68Ter-CLDN14 Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the GJB2 Gene.

Abdelaziz Tlili, Abdullah Al Mutery, Jihen Chouchen

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Frequent Collaborators

2 joint publications

Rania Harati

2 joint publications

Joudi Feras Khudeir

2 joint publications

Rifat Hamoudi

2 joint publications

Lamia Sfaihi