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| 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 | 101 | 2012 |
| Y-chromosome analysis in Egypt suggests a genetic regional continuity in Northeastern Africa F Manni, P Leonardi, A Barakat, H Rouba, E Heyer, M Klintschar, ... Human Biology, 645-658, 2002 | 94 | 2002 |
| 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 |
| Okadaic acid mimics a nuclear component required for cyclin B-cdc2 kinase microinjection to drive starfish oocytes into M phase. A Picard, JC Labbé, H Barakat, JC Cavadore, M Dorée The Journal of cell biology 115 (2), 337-344, 1991 | 82 | 1991 |
| 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 | 71 | 2012 |
| Consanguinity and inbreeding in health and disease in North African populations L Romdhane, N Mezzi, Y Hamdi, G El-Kamah, A Barakat, S Abdelhak Annual review of genomics and human genetics 20 (1), 155-179, 2019 | 70 | 2019 |
| Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies C Angebault, PO Guichet, Y Talmat-Amar, M Charif, S Gerber, ... The American Journal of Human Genetics 97 (5), 754-760, 2015 | 67 | 2015 |
| 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 | 66 | 2015 |
| Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss Y Li, E Pohl, R Boulouiz, M Schraders, G Nürnberg, M Charif, ... The American Journal of Human Genetics 86 (3), 479-484, 2010 | 65 | 2010 |
| Mutations in the protamine locus: association with spermatogenic failure? L Imken, H Rouba, B El Houate, N Louanjli, A Barakat, A Chafik, ... Molecular Human Reproduction 15 (11), 733-738, 2009 | 64 | 2009 |
| Novel mutations involving the INSL3 gene associated with cryptorchidism B El Houate, H Rouba, H Sibai, A Barakat, A Chafik, L Imken, ... The Journal of urology 177 (5), 1947-1951, 2007 | 60 | 2007 |
| Characterization of a New BLM Mutation Associated with a Topoisomerase Ilα Defect in a Patient with Bloom's Syndrome F Foucault, C Vaury, A Barakat, D Thibout, P Planchon, C Jaulin, F Praz, ... Human molecular genetics 6 (9), 1427-1434, 1997 | 57 | 1997 |
| 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 |
| Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review Z Elkarhat, Z Kindil, L Zarouf, L Razoki, J Aboulfaraj, C Elbakay, ... Journal of assisted reproduction and genetics 36, 499-507, 2019 | 49 | 2019 |
| Cdk2 activity is dispensable for the onset of DNA replication during the first mitotic cycles of the sea urchin early embryo JL Moreau, F Marques, A Barakat, P Schatt, JC Lozano, G Peaucellier, ... Developmental biology 200 (2), 182-197, 1998 | 46 | 1998 |
| The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan … H Naamane, O El Maataoui, F Ailal, A Barakat, S Bennani, J Najib, ... European journal of pediatrics 169, 1069-1074, 2010 | 43 | 2010 |
| 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 |
| Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescens G Humbert, C Delettre, A Sénéchal, C Bazalgette, A Barakat, C Bazalgette, ... Investigative ophthalmology & visual science 47 (11), 4719-4724, 2006 | 42 | 2006 |
