A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa

od Romdhane, Lilia, Mezzi, Nessrine, Dallali, Hamza, Messaoud, Olfa, Shan, Jingxuan, Fakhro, Khalid A., Kefi, Rym, Chouchane, Lotfi, Abdelhak, Sonia
izdano v NPJ Genom Med (2021)

Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort

od Landoulsi, Zied, Benromdhan, Sawssan, Ben Djebara, Mouna, Damak, Mariem, Dallali, Hamza, Kefi, Rym, Abdelhak, Sonia, Gargouri-Berrechid, Amina, Mhiri, Chokri, Gouider, Riadh
izdano v BMC Med Genet (2017)

Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases

od Bouchoucha, Sami, Chikhaoui, Asma, Najjar, Dorra, Dallali, Hamza, Khammessi, Maleke, Abdelhak, Sonia, Nessibe, Nabil, Shboul, Mohammad, Kircher, Susanne G., Al Kaissi, Ali, Yacoub-Youssef, Houda
izdano v Front Pediatr (2020)

Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa

od Hechmi, Meriem, Dallali, Hamza, Gharbi, Meriem, Jmel, Haifa, Fassatoui, Meriem, Ben Halima, Yossra, Bahri, Sonia, Bahlous, Afaf, Abid, Abdelmajid, Jamoussi, Henda, Barakat, Abdelhamid, Kefi, Rym
izdano v Biosci Rep (2020)

Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome

od Ben Haj Ali, Abir, Amouri, Ahlem, Sayeb, Marwa, Makni, Saloua, Hammami, Wajih, Naouali, Chokri, Dallali, Hamza, Romdhane, Lilia, Bashamboo, Anu, McElreavey, Kenneth, Abdelhak, Sonia, Messaoud, Olfa
izdano v Mol Genet Genomic Med (2019)

Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations

od Jmel, Haifa, Romdhane, Lilia, Ben Halima, Yosra, Hechmi, Meriem, Naouali, Chokri, Dallali, Hamza, Hamdi, Yosr, Shan, Jingxuan, Abid, Abdelmajid, Jamoussi, Henda, Trabelsi, Sameh, Chouchane, Lotfi, Luiselli, Donata, Abdelhak, Sonia, Kefi, Rym
izdano v PLoS One (2018)

Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia

od Boujemaa, Maroua, Hamdi, Yosr, Mejri, Nesrine, Romdhane, Lilia, Ghedira, Kais, Bouaziz, Hanen, El Benna, Houda, Labidi, Soumaya, Dallali, Hamza, Jaidane, Olfa, Ben Nasr, Sonia, Haddaoui, Abderrazek, Rahal, Khaled, Abdelhak, Sonia, Boussen, Hamouda, Boubaker, Mohamed Samir
izdano v PLoS One (2021)

Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins

od Jaballah-Gabteni, Amira, Tounsi, Haifa, Kabbage, Maria, Hamdi, Yosr, Elouej, Sahar, Ben Ayed, Ines, Medhioub, Mouna, Mahmoudi, Moufida, Dallali, Hamza, Yaiche, Hamza, Ben Jemii, Nadia, Maaloul, Afifa, Mezghani, Najla, Abdelhak, Sonia, Hamzaoui, Lamine, Azzouz, Mousaddak, Boubaker, Samir
izdano v J Transl Med (2019)