Fida Jbeli

Osteoprotegerin gene polymorphisms and otosclerosis: an additional genetic association study, multilocus interaction and meta-analysis

A. Souissi, Mohamed Ali Mosrati, S. Masmoudi, 2019, BMC Medical Genetics.

Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss

R. Hamoudi, Ikhlas Ben Ayed, S. Masmoudi, 2022, Frontiers in Medicine.

NADf chip, a two-color microarray for simultaneous screening of multigene mutations associated with hearing impairment in North African Mediterranean countries.

Riadh Benmarzoug, Imen Chakchouk, Mariem Ben Said, 2015, The Journal of molecular diagnostics : JMD.

8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects

A. Souissi, Ikhlas Ben Ayed, S. Masmoudi, 2021, Molecular genetics & genomic medicine.