| Consanguinity, endogamy, and genetic disorders in Tunisia N Ben Halim, N Ben Alaya Bouafif, L Romdhane, R Kefi Ben Atig, ... Journal of community genetics 4, 273-284, 2013 | 95 | 2013 |
| Deciphering the complete mitochondrial genome and phylogeny of the extinct cave bear in the Paleolithic painted cave of Chauvet C Bon, N Caudy, M De Dieuleveult, P Fosse, M Philippe, F Maksud, ... Proceedings of the National Academy of Sciences 105 (45), 17447-17452, 2008 | 93 | 2008 |
| Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East L Romdhane, R Kefi, H Azaiez, NB Halim, K Dellagi, S Abdelhak Orphanet journal of rare diseases 7, 1-11, 2012 | 80 | 2012 |
| Mitochondrial DNA sequence diversity in a sedentary population from Egypt A Stevanovitch, A Gilles, E Bouzaid, R Kefi, F Paris, RP Gayraud, ... Annals of human genetics 68 (1), 23-39, 2004 | 76 | 2004 |
| Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus M Fassatoui, M Lopez-Siles, DA Díaz-Rizzolo, H Jmel, C Naouali, ... Bioscience reports 39 (6), BSR20182348, 2019 | 52 | 2019 |
| Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss Z Riahi, H Hammami, H Ouragini, H Messai, R Zainine, Y Bouyacoub, ... Gene 525 (1), 1-4, 2013 | 42 | 2013 |
| E23K variant in KCNJ11 gene is associated with susceptibility to type 2 diabetes in the Mauritanian population I Abdelhamid, K Lasram, G Meiloud, NB Halim, R Kefi, A Samb, ... Primary Care Diabetes 8 (2), 171-175, 2014 | 41 | 2014 |
| 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 |
| A review of clinical pharmacogenetics Studies in African populations F Radouani, L Zass, Y Hamdi, J Rocha, R Sallam, S Abdelhak, S Ahmed, ... Personalized medicine 17 (2), 155-170, 2020 | 38 | 2020 |
| Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population 在突尼 … K Lasram, N Ben Halim, H Benrahma, S Mediene‐Benchekor, I Arfa, ... Journal of Diabetes 7 (1), 102-113, 2015 | 38 | 2015 |
| Phylogeny and genetic structure of Tunisians and their position within Mediterranean populations R Kefi, S Hsouna, N Ben Halim, K Lasram, L Romdhane, H Messai, ... Mitochondrial DNA 26 (4), 593-604, 2015 | 36 | 2015 |
| Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia N Ben Halim, S Hsouna, K Lasram, I Rejeb, A Walha, F Talmoudi, ... American Journal of Human Biology 28 (2), 171-180, 2016 | 35 | 2016 |
| Diversité mitochondriale de la population de Taforalt (12.000 ans BP–Maroc) une approche génétique à l'étude du peuplement de l'Afrique du nord RYM KÉFI, A STEVANOVITCH, E BOUZAID, E BÉRAUD-COLOMB Anthropologie (1962-) 43 (1), 1-12, 2005 | 31 | 2005 |
| Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia M Jerbi, M Ben Rekaya, C Naouali, M Jones, O Messaoud, H Tounsi, ... British Journal of Dermatology 174 (2), 439-443, 2016 | 28 | 2016 |
| Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort Z Landoulsi, S Benromdhan, M Ben Djebara, M Damak, H Dallali, R Kefi, ... BMC Medical Genetics 18, 1-6, 2017 | 27 | 2017 |
| Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family O Messaoud, M Ben Rekaya, R Kefi, S Chebel, ... British Journal of Dermatology 162 (4), 883-886, 2010 | 27 | 2010 |
| Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome S Elouej, H Belfki-Benali, M Nagara, K Lasram, R Attaoua, OK Sallem, ... Metabolic syndrome and related disorders 14 (2), 121-128, 2016 | 26 | 2016 |
| Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness Z Riahi, C Bonnet, R Zainine, M Louha, Y Bouyacoub, N Laroussi, ... PLoS One 9 (6), e99797, 2014 | 26 | 2014 |
| Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity O Messaoud, M Ben Rekaya, H Ouragini, S Benfadhel, H Azaiez, R Kefi, ... Archives of dermatological research 304, 171-176, 2012 | 25 | 2012 |
| Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa M Nagara, A Tiar, NB Halim, FB Rhouma, O Messaoud, Y Bouyacoub, ... Gene 527 (1), 316-320, 2013 | 24 | 2013 |
Ben Rekaya MariemPathology Department, Charles Nicolle Hospital of Tunis, Theranostic Biomarkers in cancer, UR17ES15Verified email at esstst.utm.tn
