RIAHI Awatef

Dissimilarity between sporadic, non-BRCA1/2 families and hereditary breast cancer, linked to BRCA genes, in the Tunisian population, Breast Cancer, vol. 23, N° n, pp. 807-812, Octobre 2015

RIAHI Awatef

Family history predictors of BRCA1/BRCA2 mutation status among Tunisian breast/ovarian cancer families, Breast Cancer, vol. n, N° n, Mars 2019

RIAHI Awatef, M'RAD Ridha, KHARRAT Maher

Molecular characterization, homology modeling and docking studies of the R2787H missense variation in BRCA2 gene: Association with breast cancer, Journal of Theoretical Biology, vol. 403, N° n, pp. 188-96, Août 2016

EL YOUNSI Meriem, SOUABNI KRAOUA Lilia, SAADA MEDDEB Rym, WALHA TRABELSI Mediha , OUERTANI Ines, MAAZOUL Faouzi, M'RAD Ridha

WDR73-related galloway mowat syndrome with collapsing glomerulopathy, European Journal of Scientific Research , vol. n, N° n, Octobre 2018

TRIFI CHOGRANI Manel, MAAZOUL Faouzi

Investigation of Four Genes Responsible for Autosomal Recessive Congenital Cataract and Highly Expressed in the Brain in Four Unrelated Tunisian Families, Open Journal of Ophthalmology , vol. 2, N° 3, Août 2012

WALHA TRABELSI Mediha , KHARRAT Maher, MAAZOUL Faouzi, M'RAD Ridha

Prevalence and incidence estimation of large NPHP1 homozygous deletion in Tunisian population, Pathologie Biologie, vol. n, N° n, Juin 2012