| Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco Y Naasse, H Charoute, B El Houate, C Elbekkay, L Razoki, A Malki, ... BMC urology 15, 1-6, 2015 | 65 | 2015 |
| Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case–Control Study and … H Benrahma, H Charoute, K Lasram, R Boulouiz, RKB Atig, M Fakiri, ... Biochemical genetics 52, 430-442, 2014 | 39 | 2014 |
| Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses Z Elkarhat, H Charoute, L Elkhattabi, A Barakat, H Rouba Journal of Biomolecular Structure and Dynamics 40 (1), 361-374, 2022 | 38 | 2022 |
| Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss A Bakhchane, A Bousfiha, H Charoute, S Salime, M Detsouli, K Snoussi, ... European journal of medical genetics 59 (6-7), 325-329, 2016 | 37 | 2016 |
| X-linked agammagobulinemia in a large series of North African patients: frequency, clinical features and novel BTK mutations Z Aadam, N Kechout, A Barakat, KW Chan, M Ben-Ali, I Ben-Mustapha, ... Journal of clinical immunology 36, 187-194, 2016 | 33 | 2016 |
| Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients S Ouatou, M Ajjemami, H Charoute, H Sefri, N Ghalim, H Rhaissi, ... Lipids in Health and Disease 13, 1-9, 2014 | 30 | 2014 |
| A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family. A Bakhchane, H Charoute, H Nahili, R Roky, H Rouba, M Charif, ... Gene 574 (1), 28-33, 2015 | 26 | 2015 |
| Vitamin D receptor gene polymorphisms and vitamin D status and susceptibility to type 2 diabetes mellitus in Moroccans patients E Abdeltif, H Charoute, H Barakat, H Rouba International Journal of Scientific and Research Publications 4 (8), 1-8, 2014 | 25 | 2014 |
| In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure L Elkhattabi, I Morjane, H Charoute, S Amghar, H Bouafi, Z Elkarhat, ... Journal of Diabetes Research 2019 (1), 4951627, 2019 | 23 | 2019 |
| A novel homozygous missense mutation in the FU-CRD2 domain of the R-spondin1 gene associated with familial 46, XX DSD Y Naasse, A Bakhchane, H Charoute, F Jennane, J Bignon-Topalovic, ... Sexual Development 11 (5-6), 269-274, 2018 | 22 | 2018 |
| Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population I Morjane, R Kefi, H Charoute, FL El Yaagoubi, M Hechmi, R Saile, ... Diabetes & Metabolic Syndrome: Clinical Research & Reviews 11, S853-S857, 2017 | 19 | 2017 |
| Association analysis of genetic variants with metabolic syndrome components in the Moroccan population FL El Yaagoubi, H Charoute, I Morjane, H Sefri, H Rouba, A Ainahi, ... Current Research in Translational Medicine 65 (3), 121-125, 2017 | 19 | 2017 |
| Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome M Ajjemami, S Ouatou, H Charoute, M Fakiri, H Rhaissi, H Benrahma, ... Journal of Diabetes & Metabolic Disorders 14, 1-8, 2015 | 18 | 2015 |
| Mediterranean Founder Mutation Database (MFMD): taking advantage from founder mutations in genetics diagnosis, genetic diversity and migration history of the Mediterranean … H Charoute, A Bakhchane, H Benrahma, L Romdhane, K Gabi, H Rouba, ... Human mutation 36 (11), E2441-E2453, 2015 | 17 | 2015 |
| Computational screening of potential drugs against COVID-19 disease: the Neuropilin-1 receptor as molecular target H Charoute, Z Elkarhat, L Elkhattabi, E El Fahime, N Oukkache, H Rouba, ... Virusdisease 33 (1), 23-31, 2022 | 16 | 2022 |
| The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility H Charoute, H Nahili, O Abidi, K Gabi, H Rouba, M Fakiri, A Barakat European Journal of Human Genetics 22 (3), 322-326, 2014 | 16 | 2014 |
| Prediction and structural comparison of deleterious coding nonsynonymous single nucleotide polymorphisms (nsSNPs) in human LEP gene associated with obesity H Bouafi, S Bencheikh, AL Mehdi Krami, I Morjane, H Charoute, H Rouba, ... BioMed research international 2019 (1), 1832084, 2019 | 15 | 2019 |
| TNF A −308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case–control study and meta-analysis H Sefri, H Benrahma, H Charoute, F Lakbakbi el yaagoubi, H Rouba, ... Molecular biology reports 41, 5805-5811, 2014 | 15 | 2014 |
| Compound heterozygous SLC29A3 mutation causes H syndrome in a Moroccan patient: a case report A Bakhchane, Z Kindil, H Charoute, K Benchikhi, K Khadir, S Nadifi, ... Current Research in Translational Medicine 64 (2), 65-68, 2016 | 13 | 2016 |
| Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family A Bousfiha, A Bakhchane, H Charoute, M Detsouli, H Rouba, M Charif, ... Molecular biology reports 44, 429-434, 2017 | 12 | 2017 |
Rachid SAILEVice-Président Université Hassan II de Casablanca在 univh2c.ma 的电子邮件经过验证
