Domaine de Maîtrise :
Biopathologie et Recherche Biomédicale

Domaine d’intérêt :
​Biopathologie et Recherche Biomédicale**​ ​

Les publications :
1. Moufid FZ, Bouguenouch L, El Bouchikhi I, Iraqui Houssaini M, Ouldim K. Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation. Turkish Journal of Gastroenterology 2018; 29(6):701-704.

2. Moufid FZ, Bouguenouch L, El Bouchikhi I, Chbani L, Iraqui Houssaini M, Sekal M, Belhassan K, Bennani B, Ouldim K. The first molecular screening of MLH1 and MSH2 genes in Moroccan colorectal cancer patients shows a relatively high mutational prevalence. Genetic Testing and Molecular Biomarkers; 2018; 22(8):492-497. 

3. Moufid FZ, Dieng MM, EL Bouchikhi I, Iraqui Houssaini M, Bouguenouch L, Benjelloun E, Ouldim K and Idaghdour Y. Detection of a variety of mutations in cancer predisposing genes in familial & early-onset colorectal cancer patients using targeted multigene panels. European Journal of Human Genetics 2019. Volume 27, Supplement 1: 431-432, P12.105A. 

4. Moufid FZ, Bouguenouch L, El Bouchikhi I, Iraqui Houssaini M, Belhassan K, Samri I, Laamarti RA. Ouldim K. Analyse mutationnelle des mutations germinales des gènes mlh1 et msh2 chez des patients atteints de cancer colorectal montrant une extinction des protéines MLH1 et MSH2. Revue D’Épidémiologie et de Santé Publique 2015, 63S:S79. P11.1. 

5. Moufid FZ, Bouguenouch L, El Bouchikhi I, Iraqui Houssaini M, Belhassan K, Samri I, Ouldim K. Molecular characterization of mlh1 and msh2 germline mutations among colorectal cancer patients showing extinction of MLH1 and MSH2 proteins. Basic science and epidemiology. Clinical Cancer Investigation Journal 2015; V4, Suppl S1:11-14. 

6. Moufid FZ, Bouguenouch L, El Bouchikhi I, Iraqui Houssaini M, Belhassan K, Samri I, Ouldim K. A clinicopathological and genetic study of lynch syndrome in Morocco. European Journal of Human Genetics 2015. Volume 23, E-Supplement 1:341.PS18.59.