| Issue Date | Title | Author(s) |
| 2010 | The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: Evidence for a founder effect in the Moroccan population | Naamane, Hamid; El Maataoui, Ouafaa; Ailal, Fatima; Barakat, Abdelhamid; Bennani, Siham; Najib, Jilali; Hassar, Mohammed; Saile, Rachid; Bousfiha, Ahmed Aziz |
| 2012 | Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a moroccan population | Benrahma, Houda; Abidi, Omar; Melouk, Leila; Ajjemami, Maria; Rouba, Hassan; Chadli, Asmaa; Oudghiri, Mounia; Farouqui, Ahmed; Barakat, Abdelhamid; Rouba, Hassan; Chadli, Asmaa; Oudghiri, Mounia; Farouqui, Ahmed; Barakat, Abdelhamid |
| 2012 | Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a moroccan population | Benrahma, Houda; Abidi, Omar; Melouk, Leila; Ajjemami, Maria; Rouba, Hassan; Chadli, Asmaa; Farouqui, Ahmed; Barakat, Abdelhamid |
| 2013 | C.1643-1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum | Senhaji, Mohamed Amine; Abidi, Omar; Nadifi, Sellama; Benchikhi, Hakima; Khadir, Khadija; Ben Rekaya, Mariem; Eloualid, Abdelmajid; Messaoud, Olfa; Abdelhak, Sonia; Barakat, Abdelhamid |
| 2013 | Clinicopathological Features and Molecular Analysis of Primary Glioblastomas in Moroccan Patients | HILMANI, SAID; Abidi, Omar; Benrahma, Houda; Karkouri, Mehdi; Sahraoui, Souha; El Azhari, Abdessamad; Barakat, Abdelhamid |
| 2017 | Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families | Salime, Sara; Charif, Majida; Bousfiha, Amale; Elrharchi, Soukaina; Bakhchane, Amina; Charoute, Hicham; Kabine, Mostafa; Snoussi, Khalid; Lenaers, Guy; Barakat, Abdelhamid |
| 2011 | Maternal effect and familial aggregation in a type 2 diabetic moroccan population | Benrahma, Houda; Arfa, Imen; Charif, Majida; Bounaceur, Safaa; Eloualid, Abdelmajid; Boulouiz, Redouane; Nahili, Halima; Abidi, Omar; Rouba, Hassan; Chadli, Asmaa; Oudghiri, Mounia; Farouqui, Ahmed; Abdelhak, Sonia; Barakat, Abdelhamid |
| 2011 | Maternal effect and familial aggregation in a type 2 diabetic moroccan population | Benrahma, Houda; Arfa, Imen; Charif, Majida; Bounaceur, Safaa; Eloualid, Abdelmajid; Boulouiz, Redouane; Nahili, Halima; Abidi, Omar; Rouba, Hassan; Chadli, Asmaa; Oudghiri, Mounia; Farouqui, Ahmed; Abdelhak, Sonia; Barakat, Abdelhamid |
| 2008 | No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population | El Houate, Brahim; Rouba, Hassan; Imken, Laila; Sibai, Hicham; Chafik, Abdelaziz; Boulouiz, Redouane; Chadli, Elbakkay; Hassar, Mohmmed; McElreavey, Ken; Barakat, Abdelhamid |
| 2015 | A novel mutation in the ABCD1 gene of a Moroccan patient with X-linked adrenoleukodystrophy: Case report | Karkar, Adnane; Barakat, Abdelhamid; Bakhchane, Amina; Fettah, Houda; Slassi, Ilham; Dorboz, Imen; Boespflug-Tanguy, Odile; Nadifi, Sellama |
| 2015 | A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family. | Bakhchane, Amina; Charoute, Hicham; Nahili, Halima; Roky, Rachida; Rouba, Hassan; Charif, Majida; Lenaers, Guy; Barakat, Abdelhamid |
| 2007 | Novel Mutations Involving the INSL3 Gene Associated With Cryptorchidism | El Houate, Brahim; Rouba, Hassan; Sibai, Hassan; Barakat, Abdelhamid; Chafik, Abdelaziz; Chadli, El bekkay; Imken, Laila; V. Bogatcheva, Natalia; Feng, Shu; I. Agoulnik, Alexander; McElreavey, Ken |
| 2015 | Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients | El Khachibi, Meryam; Diakite, Brehima; Hamzi, Khalil; Badou, Abdallah; Senhaji, Mohamed Amine; Bakhchane, Amina; Jouhadi, Hassan; Barakat, Abdelhamid; Benider, Abdellatif; Nadifi, Sellama |
| 2008 | Three new BLM gene mutations associated with Bloom syndrome | Amor-Gue´ret, Mounira; Dubois-d’Enghien, Catherine; Lauge´, Anthony; Onclercq-Delic, Rosine; Barakat, Abdelhamid; Chadli, Elbekkay; Aziz Bousfiha, Ahmed; Benjelloun, Meriem; Flori, Elisabeth; Doray, Be´re´nice; Laugel, Vincent; Lourenc, Maria Teresa; Gonc¸alves, Rui; Sousa, Silvia; Couturier, Je´roˆme; Stoppa-Lyonnet, Dominique |
| 2016 | Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss | Bakhchane, Amina; Bousfiha, Amale; Charoute, Hicham; Salime, Sara; Detsouli, Mustapha; Snoussi, Khalid; Nadifi, Sellama; Kabine, Mostafa; Rouba, Hassan; Dehbi, Hind; Roky, Rachida; Charif, Majida; Barakat, Abdelhamid |
| 2016 | Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss | Bakhchane, Amina; Bousfiha, Amale; Charoute, Hicham; Salime, Sara; Detsouli, Mustapha; Snoussi, Khalid; Nadifi, Sellama; Kabine, Mostafa; Rouba, Hassan; Dehbi, Hind; Roky, Rachida; Charif, Majida; Barakat, Abdelhamid |
| 2016 | X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency Clinical Features and Novel BTK Mutations | Aadam, Zahra; Kechout, Nadia; Barakat, Abdelhamid; Chan, Koon-Wing; Ben-Ali, Meriem; Ben-Mustapha, Imen; Zidi, Fethi; Ailal, Fatima; Attal, Nabila; Doudou, Fatouma; Abbadi, Mohamed-Cherif; Kaddache, Chawki; Smati, Leila; Touri, Nabila; Chemli, Jalel; Gargah, Tahar; Brini, Ines; Bakhchane, Amina; Charoute, Hicham; Jeddane, Leila; El Atiqi, Sara; El Hafidi, Naïma; Hida, Mustapha; Saile, Rachid; Salih Alj, Hanane; Boukari, Rachida; Bejaoui, Mohamed; Najib, Jilali; Barbouche, Mohamed-Ridha; Lau, Yu-Lung; Mellouli, Fethi; Bousfiha, Ahmed Aziz |
