| Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation M Kharrat, V Tardy, R M’Rad, F Maazoul, LB Jemaa, M Refaï, Y Morel, ... The Journal of Clinical Endocrinology & Metabolism 89 (1), 368-374, 2004 | 108 | 2004 |
| Mutation spectrum and prevalence of BRCA1 and BRCA2 genes in patients with familial and early‐onset breast/ovarian cancer from Tunisia A Riahi, M Kharrat, ME Ghourabi, F Khomsi, A Gamoudi, I Lariani, AE May, ... Clinical Genetics 87 (2), 155-160, 2015 | 55 | 2015 |
| MEFV mutations in Tunisian patients suffering from familial Mediterranean fever HB Chaabouni, M Ksantini, R M’rad, M Kharrat, M Chaabouni, F Maazoul, ... Seminars in arthritis and rheumatism 36 (6), 397-401, 2007 | 52 | 2007 |
| Only two mutations detected in 15 Tunisian patients with 11β‐hydroxylase deficiency: the p. Q356X and the novel p. G379V M Kharrat, S Trabelsi, M Chaabouni, F Maazoul, L Kraoua, L Ben Jemaa, ... Clinical genetics 78 (4), 398-401, 2010 | 39 | 2010 |
| Comparative genomic signature representations of the emerging COVID-19 coronavirus and other coronaviruses: High identity and possible recombination between Bat and Pangolin … R Touati, S Haddad-Boubaker, I Ferchichi, I Messaoudi, AE Ouesleti, ... Genomics 112 (6), 4189-4202, 2020 | 38 | 2020 |
| An Immunoscore System Based On CD3+ And CD8+ Infiltrating Lymphocytes Densities To Predict The Outcome Of Patients With Colorectal Adenocarcinoma M Trabelsi, F Farah, B Zouari, MH Jaafoura, M Kharrat OncoTargets and therapy, 8663-8673, 2019 | 37 | 2019 |
| A genome‐wide RNA i screen reveals essential therapeutic targets of breast cancer stem cells A Arfaoui, C Rioualen, V Azzoni, G Pinna, P Finetti, J Wicinski, E Josselin, ... EMBO Molecular Medicine 11 (10), e9930, 2019 | 28 | 2019 |
| Prevalence of BRCA1 and BRCA2 large genomic rearrangements in Tunisian high risk breast/ovarian cancer families: Implications for genetic testing A Riahi, H Chabouni-Bouhamed, M Kharrat Cancer genetics 210, 22-27, 2017 | 26 | 2017 |
| Detection of a frequent duplicated CYP21A2 gene carrying a Q318X mutation in a general population with quantitative PCR methods M Kharrat, A Riahi, F Maazoul, R M'rad, H Chaabouni Diagnostic Molecular Pathology 20 (2), 123-127, 2011 | 26 | 2011 |
| Tolllike receptor 4 (TLR4) polymorphisms in Tunisian patients with Crohn's disease: genotype-phenotype correlation L Zouiten-Mekki, M Kharrat, S Karoui, M Serghimi, M Fekih, S Matri, ... BMC gastroenterology 9, 1-6, 2009 | 26 | 2009 |
| In silico comparative study of SARS-CoV-2 proteins and antigenic proteins in BCG, OPV, MMR and other vaccines: evidence of a possible putative protective effect S Haddad-Boubaker, H Othman, R Touati, K Ayouni, M Lakhal, ... BMC bioinformatics 22, 1-14, 2021 | 25 | 2021 |
| Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy SN Manivannan, S Darouich, A Masmoudi, D Gordon, G Zender, Z Han, ... PLoS genetics 16 (5), e1008639, 2020 | 25 | 2020 |
| Testicular adrenal rest tumours in young adult males with congenital adrenal hyperplasia: Prevalence and impact on testicular function SH Chihaoui M, Kanoun F, Chaker F, Yazidi M, Bouchrit K, Mizouni H, Feki M ... Andrologia 48 (1), 45-50, 2016 | 22 | 2016 |
| Exome sequencing and case–control analyses identify RCC1 as a candidate breast cancer susceptibility gene A Riahi, H Radmanesh, P Schürmann, N Bogdanova, R Geffers, ... International Journal of Cancer 142 (12), 2512-2517, 2018 | 21 | 2018 |
| New intraclass helitrons classification using DNA-image sequences and machine learning approaches R Touati, I Messaoudi, AE Oueslati, Z Lachiri, M Kharrat Irbm 42 (3), 154-164, 2021 | 20 | 2021 |
| Response to clopidogrel and of the cytochrome CYP2C19 gene polymorphism. R Charfi, K Mzoughi, M Boughalleb, H Hosni, S Kouidhi, I Sfar, ... La Tunisie medicale 96 (3), 209-218, 2018 | 18 | 2018 |
| Consanguinity and homozygosity among Tunisian patients with an autosomal recessive disorder W Kelmemi, I Chelly, M Kharrat, H Chaabouni-Bouhamed Journal of Biosocial Science 47 (6), 718-726, 2015 | 18 | 2015 |
| Crohn's disease and polymorphism of heat shock protein gene HSP70-2 in the Tunisian population L Zouiten-Mekki, S Karoui, M Kharrat, M Fekih, S Matri, J Boubaker, ... European journal of gastroenterology & hepatology 19 (3), 225-228, 2007 | 16 | 2007 |
| Phytotoxic effects of essential oil from Eucalyptus cinerea and its physiological mechanisms A Grichi, Z Nasr, ML Khouja, Y Zaouchi Journal of New Sciences 15, 2016 | 14 | 2016 |
| High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families A Riahi, M Kharrat, I Lariani, H Chaabouni-Bouhamed Familial cancer 13, 603-609, 2014 | 14 | 2014 |
