Concepedia

Abdelaziz Tlili

AT

Statistics

Publications

34

Citations

1.1K

H-Index

20

Active since

2003

Affiliations

University of Sharjah(Current)

Hopital Universitaire Habib Bourguiba

University of Sfax

Centre of Biotechnology of Sfax

Hopital Universitaire Hedi Chaker

Abdelaziz Tlili is an author at University of Sharjah specializing in molecular genetics, life sciences, and genetics.

ORCID

Publications per year

2003–2022

34

Publications

34

Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome

Didier Dulon, Samantha Papal, Pranav Patni et al. · Journal of Clinical Investigation · 2018 · 138 citations · Full text

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Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay et al. · Nature Genetics · 2008 · 87 citations · Full text

, , +15

CDC14A phosphatase is essential for hearing and male fertility in mouse and human

Ayesha Imtiaz, Inna A. Belyantseva, Alisha Beirl et al. · Human Molecular Genetics · 2017 · 62 citations · Full text

, , +15

<i>TMC1</i> but Not <i>TMC2</i> Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families

Abdelaziz Tlili, Imen Ben Rebeh, Houria Dhouib et al. · Audiology and Neurotology · 2008 · 59 citations

, , +16

Loss of miR-101-3p Promotes Transmigration of Metastatic Breast Cancer Cells through the Brain Endothelium by Inducing COX-2/MMP1 Signaling

Rania Harati, Mohammad G. Mohammad, Abdelaziz Tlili et al. · Pharmaceuticals · 2020 · 51 citations · Full text

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1–5 of 34