| Noonan syndrome-causing genes: molecular update and an assessment of the mutation rate I El Bouchikhi, K Belhassan, FZ Moufid, MI Houssaini, L Bouguenouch, ... International Journal of Pediatrics and Adolescent Medicine 3 (4), 133-142, 2016 | 84 | 2016 |
| Williams–Beuren syndrome in diverse populations P Kruszka, AR Porras, DH De Souza, A Moresco, V Huckstadt, AD Gill, ... American Journal of Medical Genetics Part A 176 (5), 1128-1136, 2018 | 79 | 2018 |
| Helicobacter pylori CagA EPIYA-C motifs and gastric diseases in Moroccan patients M El Khadir, SA Boukhris, DA Benajah, SA Ibrahimi, L Chbani, ... Infection, Genetics and Evolution 66, 120-129, 2018 | 23 | 2018 |
| High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast–ovarian cancer … FZ Laarabi, I Ratbi, SC Elalaoui, L Mezzouar, Y Doubaj, L Bouguenouch, ... BMC Research Notes 10, 1-5, 2017 | 22 | 2017 |
| Associations between nutritional factors and KRAS mutations in colorectal cancer: a systematic review A El Asri, B Zarrouq, K El Kinany, L Bouguenouch, K Ouldim, K El Rhazi BMC cancer 20 (1), 696, 2020 | 15 | 2020 |
| Analysis of molecular pretreated tumor profiles as predictive biomarkers of therapeutic response and survival outcomes after neoadjuvant therapy for rectal cancer in moroccan … I El Otmani, F El Agy, S El Baradai, L Bouguenouch, N Lahmidani, ... Disease Markers 2020 (1), 8459303, 2020 | 13 | 2020 |
| The first PTPN11 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to the previous studies IEL BOUCHIKHI, I Samri, MI Houssaini, S Trhanint, L Bouguenouch, ... Turkish Journal of Medical Sciences 45 (2), 306-312, 2015 | 8 | 2015 |
| Correlation of epidermal growth factor receptor mutation with major histologic subtype of lung adenocarcinoma according to IASLC/ATS/ERS classification S Boukansa, Z Benbrahim, S Gamrani, S Bardai, L Bouguenouch, A Mazti, ... Cancer Control 29, 10732748221084930, 2022 | 7 | 2022 |
| Dietary Fat Intake and KRAS Mutations in Colorectal Cancer in a Moroccan Population A El Asri, K Ouldim, L Bouguenouch, M Sekal, FZ Moufid, E Kampman, ... Nutrients 14 (2), 318, 2022 | 7 | 2022 |
| GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot IEL Bouchikhi, K Belhassan, FZ Moufid, MI Houssaini, L Bouguenouch, ... African Health Sciences 18 (4), 922-930, 2018 | 7 | 2018 |
| Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age I El Bouchikhi, L Bouguenouch, FZ Moufid, I Samri, F Abdouss, ... Egyptian Journal of Medical Human Genetics 21, 1-9, 2020 | 6 | 2020 |
| New biomarkers and treatment advances in triple-negative breast cancer B El Hejjioui, S Lamrabet, S Amrani Joutei, N Senhaji, T Bouhafa, ... Diagnostics 13 (11), 1949, 2023 | 4 | 2023 |
| Molecular and clinical assessment of maturity-onset diabetes of the young revealed low mutational rate in Moroccan families S Trhanint, L Bouguenouch, S Abourazzak, H El Ouahabi, H Latrech, ... International Journal of Pediatrics and Adolescent Medicine 9 (2), 98-103, 2022 | 4 | 2022 |
| 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 I El Bouchikhi, L Bouguenouch, FZ Moufid, K Belhassan, I Samri, ... The Eurasian Journal of Medicine 52 (3), 283, 2020 | 4 | 2020 |
| Genomic evidence of multiple SARS-CoV-2 introductions into Morocco B Chaouni, I Allali, S Sehli, W Rhalem, AI Azami, N Habib, S Hamdi, ... F1000Research 9 (679), 679, 2020 | 4 | 2020 |
| Kallmann-de Morsier syndrome: about 3 cases H Marhari, CO FZ, HE Ouahabi, L Bouguenouch The Pan African Medical Journal 33, 221-221, 2019 | 4 | 2019 |
| The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational Prevalence FZ Moufid, L Bouguenouch, I El Bouchikhi, L Chbani, M Iraqui Houssaini, ... Genetic Testing and Molecular Biomarkers 22 (8), 492-497, 2018 | 4 | 2018 |
| NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population. I El Bouchikhi, L Bouguenouch, FZ Moufid, MI Houssaini, K Belhassan, ... Anatolian Journal of Cardiology/Anadolu Kardiyoloji Dergisi 17 (3), 2017 | 4 | 2017 |
| Syndrome de Lynch: à propos d'un cas et revue de la litterature L Bouguenouch, I Samri, K Belhassan, H Sayel, M Abbassi, S Bennis, ... The pan African medical journal 24, 2016 | 4 | 2016 |
| Case Report-Le syndrome de Cri du Chat: A propos d’une observation K Ouldim, I Samri, L Bouguenouch, H Hamdaoui, I El Otmani, M Hbibi, ... Pan African Medical Journal 11 (1), 2012 | 4 | 2012 |
