| A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss S Von Ameln, G Wang, R Boulouiz, MA Rutherford, GM Smith, Y Li, ... The American Journal of Human Genetics 91 (5), 919-927, 2012 | 100 | 2012 |
| AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men L Imken, B El Houate, A Chafik, H Nahili, R Boulouiz, O Abidi, E Chadli, ... Asian journal of andrology 9 (5), 674-678, 2007 | 85 | 2007 |
| Association of the MTHFR A1298C Variant with Unexplained Severe Male Infertility A Eloualid, O Abidi, M Charif, B El Houate, H Benrahma, N Louanjli, ... PloS one 7 (3), e34111, 2012 | 68 | 2012 |
| Association of spermatogenic failure with the b2/b3 partial AZFc deletion A Eloualid, H Rhaissi, A Reguig, S Bounaceur, B El Houate, O Abidi, ... PloS one 7 (4), e34902, 2012 | 56 | 2012 |
| GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation O Abidi, R Boulouiz, H Nahili, M Ridal, MN Alami, A Tlili, H Rouba, ... International journal of pediatric otorhinolaryngology 71 (8), 1239-1245, 2007 | 55 | 2007 |
| Association of the C677T Polymorphism in the Human Methylenetetrahydrofolate Reductase (MTHFR) Gene with the Genetic Predisposition for Type 2 Diabetes … H Benrahma, O Abidi, L Melouk, M Ajjemami, H Rouba, A Chadli, ... Genetic testing and molecular biomarkers 16 (5), 383-387, 2012 | 42 | 2012 |
| Genetics of breast cancer in African populations: a literature review A Abbad, H Baba, H Dehbi, M Elmessaoudi-Idrissi, Z Elyazghi, O Abidi, ... Global health, epidemiology and genomics 3, e8, 2018 | 36 | 2018 |
| The prevalence of resistance-associated mutations to protease and reverse transcriptase inhibitors in treatment-naive (HIV1)-infected individuals in Casablanca, Morocco K Bakhouch, A Oulad-Lahcen, R Bensghir, M Blaghen, KM Elfilali, ... The Journal of Infection in Developing Countries 3 (05), 380-391, 2009 | 35 | 2009 |
| The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population M Charif, S Bounaceur, O Abidi, H Nahili, H Rouba, M Kandil, R Boulouiz, ... Molecular biology reports 39 (12), 11011-11016, 2012 | 31 | 2012 |
| Maternal effect and familial aggregation in a type 2 diabetic Moroccan population H Benrahma, I Arfa, M Charif, S Bounaceur, A Eloualid, R Boulouiz, ... Journal of Community Health 36, 943-948, 2011 | 29 | 2011 |
| Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss H Nahili, M Charif, R Boulouiz, H Benrahma, O Abidi, A Chafik, H Rouba, ... International journal of pediatric otorhinolaryngology 74 (9), 1071-1074, 2010 | 27 | 2010 |
| Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness H Nahili, M Ridal, R Boulouiz, O Abidi, L Imken, H Rouba, MN Alami, ... International journal of pediatric otorhinolaryngology 72 (11), 1633-1636, 2008 | 27 | 2008 |
| Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma O Abidi, S Knari, H Sefri, M Charif, A Senechal, C Hamel, H Rouba, ... Molecular vision 17, 3541, 2011 | 25 | 2011 |
| c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum MA Senhaji, O Abidi, S Nadifi, H Benchikhi, K Khadir, M Ben Rekaya, ... Archives of Dermatological Research 305, 53-57, 2013 | 22 | 2013 |
| A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family R Boulouiz, Y Li, H Soualhine, O Abidi, A Chafik, G Nürnberg, C Becker, ... American journal of medical genetics Part A 146 (23), 3086-3089, 2008 | 19 | 2008 |
| Clinicopathological features and molecular analysis of primary glioblastomas in Moroccan patients S Hilmani, O Abidi, H Benrahma, M Karkouri, S Sahraoui, A El Azhari, ... Journal of Molecular Neuroscience 49, 567-573, 2013 | 18 | 2013 |
| Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss M Charif, O Abidi, R Boulouiz, H Nahili, H Rouba, M Kandil, B Delprat, ... Biochemical and biophysical research communications 419 (4), 643-647, 2012 | 18 | 2012 |
| 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 | 17 | 2014 |
| The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population O Abidi, R Boulouiz, H Nahili, L Imken, H Rouba, A Chafik, A Barakat Biochemical and biophysical research communications 377 (3), 971-974, 2008 | 16 | 2008 |
| 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 |
