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Page 1
Dietary Fat Intake and KRAS Mutations in Colorectal Cancer in a Moroccan Population.
El Asri A, Ouldim K, Bouguenouch L, Sekal M, Moufid FZ, Kampman E, Huybrechts I, Gunter MJ, Abbaoui S, Znati K, Karkouri M, Kinany KE, Hatime Z, Deoula MMS, Chbani L, Zarrouq B, El Rhazi K. El Asri A, et al. Among authors: moufid fz. Nutrients. 2022 Jan 13;14(2):318. doi: 10.3390/nu14020318. Nutrients. 2022. PMID: 35057499 Free PMC article.
Molecular and clinical assessment of maturity-onset diabetes of the young revealed low mutational rate in Moroccan families.
Trhanint S, Bouguenouch L, Abourazzak S, El Ouahabi H, Latrech H, Benyakhlef S, Bennani B, El Bouchikhi I, Moufid FZ, Ouldim K, El Ghadraoui L, Maazouzi N. Trhanint S, et al. Among authors: moufid fz. Int J Pediatr Adolesc Med. 2022 Jun;9(2):98-103. doi: 10.1016/j.ijpam.2021.03.006. Epub 2021 Mar 22. Int J Pediatr Adolesc Med. 2022. PMID: 35663783 Free PMC article.
Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.
El Bouchikhi I, Bouguenouch L, Moufid FZ, Belhassan K, Samri I, Chaouti A, Houssaïni MI, Atmani S, Ouldim K. El Bouchikhi I, et al. Among authors: moufid fz. Eurasian J Med. 2020 Oct;52(3):283-287. doi: 10.5152/eurasianjmed.2020.19237. Eurasian J Med. 2020. PMID: 33209082 Free PMC article.
Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate.
El Bouchikhi I, Belhassan K, Moufid FZ, Iraqui Houssaini M, Bouguenouch L, Samri I, Atmani S, Ouldim K. El Bouchikhi I, et al. Among authors: moufid fz. Int J Pediatr Adolesc Med. 2016 Dec;3(4):133-142. doi: 10.1016/j.ijpam.2016.06.003. Epub 2016 Aug 18. Int J Pediatr Adolesc Med. 2016. PMID: 30805484 Free PMC article. Review.
Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016.
Srivastava AK, Wang Y, Huang R, Skinner C, Thompson T, Pollard L, Wood T, Luo F, Stevenson R, Polimanti R, Gelernter J, Lin X, Lim IY, Wu Y, Teh AL, Chen L, Aris IM, Soh SE, Tint MT, MacIsaac JL, Yap F, Kwek K, Saw SM, Kobor MS, Meaney MJ, Godfrey KM, Chong YS, Holbrook JD, Lee YS, Gluckman PD, Karnani N; GUSTO study group; Kapoor A, Lee D, Chakravarti A, Maercker C, Graf F, Boutros M, Stamoulis G, Santoni F, Makrythanasis P, Letourneau A, Guipponi M, Panousis N, Garieri M, Ribaux P, Falconnet E, Borel C, Antonarakis SE, Kumar S, Curran J, Blangero J, Chatterjee S, Kapoor A, Akiyama J, Auer D, Berrios C, Pennacchio L, Chakravarti A, Donti TR, Cappuccio G, Miller M, Atwal P, Kennedy A, Cardon A, Bacino C, Emrick L, Hertecant J, Baumer F, Porter B, Bainbridge M, Bonnen P, Graham B, Sutton R, Sun Q, Elsea S, Hu Z, Wang P, Zhu Y, Zhao J, Xiong M, Bennett DA, Hidalgo-Miranda A, Romero-Cordoba S, Rodriguez-Cuevas S, Rebollar-Vega R, Tagliabue E, Iorio M, D’Ippolito E, Baroni S, Kaczkowski B, Tanaka Y, Kawaji H, Sandelin A, Andersson R, Itoh M, Lassmann T; The FANTOM5 Consortium; Hayashizaki Y, Carninci P, Forrest ARR, Semple CA, Rosenthal EA, Shirts B, Amendola L, Gallego C, Horike-Pyne… See abstract for full author list ➔ Srivastava AK, et al. Among authors: moufid fz. Hum Genomics. 2016 May 26;10 Suppl 1(Suppl 1):12. doi: 10.1186/s40246-016-0063-5. Hum Genomics. 2016. PMID: 27294413 Free PMC article.