R. Meddeb

Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation

R. M’rad, S. Hannachi, Hela Sassi, 2022, BMC medical genomics.

Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene

T. Dörk, R. Geffers, N. Bogdanova, 2018, Geburtshilfe und Frauenheilkunde.

Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk

S. Abdelhak, O. Messaoud, M. B. rekaya, 2020 .

Identification of Novel BRCA1 Germline Deleterious Variant Among a Tunisian Family

K. Mrad, K. Rahal, S. Hannachi, 2021, Clinical Oncology and Research.

WDR73-related galloway mowat syndrome with collapsing glomerulopathy.

I. Ouertani, R. M’rad, L. Kraoua, 2019, European journal of medical genetics.

Clinical utility of circulating DNA analysis for rapid detection of actionable mutations to select metastatic colorectal patients for anti-EGFR treatment

M. Ychou, E. Assenat, C. Borg, 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients

I. Ouertani, H. Azzouz, L. Kraoua, 2014 .

Phenotype Spectrum in Tunisian Population with NPHP1 Deletion

R. Meddeb, Y. Hammi, T. Gargah, 2023, Indian Journal of Nephrology.