Tlili Abdelaziz
University of Sharjah
H-index: 20
Asia-United Arab Emirates
Top articles of Tlili Abdelaziz
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on … | Metabolic Brain Disease | Marwa Maalej Lamia Sfaihi Olfa-Alila Fersi Boudour Khabou Marwa Ammar | 2024/2/16 |
Highly efficient, label free, ultrafast plasmonic SERS biosensor (silver nanoarrays/Si) to detect GJB2 gene expressed deafness mutations in real time validated with PCR studies | International Journal of Biological Macromolecules | Arwa AI AlSafadi Krithikadevi Ramachandran Soumya Columbus Abdelaziz Tlili Kais Daoudi | 2024/2/1 |
Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene | Gene | Olfa Alila-Fersi Amel Tej Marwa Maalej Marwa Kharrat Lamia Boughamoura | 2024/7/1 |
Expanding the genetic and phenotypic spectrum of TRAPPC9 and MID2-related neurodevelopmental disabilities: report of two novel mutations, 3D-modelling, and molecular docking … | Journal of Human Genetics | Marwa Kharrat Chahnez Triki Abir ben isaa Wafa Bouchaala Olfa Alila | 2024/3/11 |
Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss | Saudi Journal of Biological Sciences | Abdullah Al Mutery Walaa Kamal Eldin Mohamed Mona Mahfood Jihen Chouchen Abdelaziz Tlili | 2023/2/1 |
A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation … | Metabolic Brain Disease | Ameni Aguech Lamia Sfaihi Olfa Alila-Fersi Roeya Kolsi Abdelaziz Tlili | 2023/12 |
A Novel Mutation in the MAP7D3 Gene in Two Siblings with Severe Intellectual Disability and Autistic Traits: Concurrent Assessment of BDNF Functional Polymorphism, X … | Journal of Molecular Neuroscience | Marwa Kharrat Abir Ben Issa Abdelaziz Tlili Olfa Jallouli Olfa Alila-Fersi | 2023/10 |
Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families | Human Genomics | Maria Asaad Mona Mahfood Abdullah Al Mutery Abdelaziz Tlili | 2023/5/15 |
Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region | Frontiers in Neurology | Ikhlas Ben Ayed Olfa Jallouli Yoshiko Murakami Amal Souissi Salma Mallouli | 2023/3/9 |
Dual phenomenon of surface plasmon and laser optics induced EM enhancement for rapid DNA detection with semiconductor nanostructures (SiNWs/AgNPs) | Journal of Physics: Conference Series | Krithikadevi Ramachandran Kais Dauodi Soumya Columbus Abdelaziz Tlili Mounir Gaidi | 2022/8/1 |
Genetic etiology of hereditary hearing loss in the Gulf cooperation council countries | Abdullah Al Mutery Mona Mahfood Jihen Chouchen Abdelaziz Tlili | 2022/4 | |
Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment | Journal of Biomolecular Structure and Dynamics | Amal Souissi Dorra Abdelmalek Driss Imen Chakchouk Mariem Ben Said Ikhlas Ben Ayed | 2022/12/5 |
miR-27a-3p regulates expression of intercellular junctions at the brain endothelium and controls the endothelial barrier permeability | PLoS One | Rania Harati Saba Hammad Abdelaziz Tlili Mona Mahfood Aloïse Mabondzo | 2022/1/13 |
First description of the MEGDEHL syndrome in the Tunisian population via whole‐exome sequencing: Novel nonsense mutation in SERAC1 gene | International Journal of Developmental Neuroscience | Rahma Felhi Kamel Monastiri Hayet Ben Hamida Marwa Ammar Fatma Zohra Chioukh | 2022/12 |
miR-623 targets metalloproteinase-1 and attenuates extravasation of brain metastatic triple-negative breast cancer cells | Breast Cancer: Targets and Therapy | Dua Hammash Mona Mahfood Ghalia Khoder Munazza Ahmed Abdelaziz Tlili | 2022/1/1 |
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational … | International Journal of Developmental Neuroscience | Marwa Ammar Wajdi Safi Abdelaziz Tlili Olfa Alila‐Fersi Fakher Frikha | 2022/11 |
Identification of a novel homozygous mutation in NAXE gene associated with early-onset progressive encephalopathy by whole-exome sequencing: in silico protein structure … | neurogenetics | Marwa Maalej Lamia Sfaihi Marwa Ammar Fakher Frikha Marwa Kharrat | 2022/10 |
Tuning the nanostructural properties of silver nanoparticles for optimised surface enhanced Raman scattering sensing of SARS CoV-2 spike protein | Advances in Natural Sciences: Nanoscience and Nanotechnology | Kais Daoudi Krithikadevi Ramachandran Soumya Columbus Abdelaziz Tlili Mona Mahfood | 2021/9/27 |
Fast, highly sensitive and label free detection of small genetic sequence difference of DNA using novel Surface-Enhanced Raman Spectroscopy nanostructured sensor | Sensing and Bio-Sensing Research | Mounir Gaidi Kais Daoudi Abdelaziz Tlili Soumya Columbus Joël Leblanc-Lavoie | 2021/6/1 |
Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations | International Journal of Pediatric Otorhinolaryngology | Jihen Chouchen Mona Mahfood Maryam Alobathani Walaa Kamal Eldin Mohamed Abdelaziz Tlili | 2021/1/1 |
