| Seroprevalence of Helicobacter pylori in Nahavand: a population-based study AHM Alizadeh, S Ansari, M Ranjbar, HM Shalmani, I Habibi, M Firouzi, ... EMHJ-Eastern Mediterranean Health Journal, 15 (1), 129-135, 2009, 2009 | 62 | 2009 |
| Functional polymorphisms of PTPN22 and FcgR genes in Tunisian patients with rheumatoid arthritis I Sfar, T Dhaouadi, I Habibi, L Abdelmoula, M Makhlouf, TB Romdhane, ... Archives de l'Institut Pasteur de Tunis 86 (1-4), 51, 2009 | 27 | 2009 |
| Identifying mutations in Tunisian families with retinal dystrophy I Habibi, A Chebil, Y Falfoul, N Allaman-Pillet, F Kort, DF Schorderet, ... Scientific reports 6 (1), 37455, 2016 | 26 | 2016 |
| Interleukin-18 gene polymorphisms in tunisian patients with inflammatory bowel disease W Ben Aleya, I Sfar, I Habibi, L Mouelhi, H Aouadi, M Makhlouf, ... Digestion 83 (4), 269-274, 2011 | 26 | 2011 |
| Effect of risk alleles in CFH, C3, and VEGFA on the response to intravitreal bevacizumab in Tunisian patients with neovascular age-related macular degeneration I Habibi, F Kort, I Sfar, A Chebil, R Bouraoui, TB Abdallah, Y Gorgi, ... Klinische Monatsblätter für Augenheilkunde 233 (04), 465-470, 2016 | 18 | 2016 |
| Clinical and genetic findings of autosomal recessive bestrophinopathy (ARB) I Habibi, Y Falfoul, MG Todorova, S Wyrsch, V Vaclavik, M Helfenstein, ... Genes 10 (12), 953, 2019 | 16 | 2019 |
| Vascular endothelial growth factor genetic polymorphisms and susceptibility to age-related macular degeneration in Tunisian population I Habibi, I Sfar, A Chebil, F Kort, R Bouraoui, S Jendoubi-Ayed, ... Biomarker research 2, 1-8, 2014 | 15 | 2014 |
| Genetic spectrum of retinal dystrophies in Tunisia I Habibi, Y Falfoul, A Turki, A Hassairi, K El Matri, A Chebil, DF Schorderet, ... Scientific reports 10 (1), 11199, 2020 | 14 | 2020 |
| Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa I Habibi, A Chebil, F Kort, DF Schorderet, L El Matri Ophthalmic genetics 38 (5), 494-497, 2017 | 13 | 2017 |
| Y402H polymorphism in complement factor H and age-related macular degeneration in the Tunisian population I Habibi, I Sfar, F Kort, H Aounallah-Skhiri, A Chebil, I Chouchene, ... Ophthalmic research 49 (4), 177-184, 2013 | 13 | 2013 |
| Motifs du recours aux services durgence des principaux hôpitaux du Grand Tunis HL Ben Gobrane, H Aounallah-Skhiri, A Ben Hamida, N Somrani, ... Eastern Mediterranean Health Journal 18 (1), 56-65, 2012 | 12 | 2012 |
| Genotype-phenotype correlation in ten Tunisian families with non-syndromic retinitis pigmentosa A Chebil, Y Falfoul, I Habibi, F Munier, D Schorderet, L El Matri Journal francais d'ophtalmologie 39 (3), 277-286, 2016 | 9 | 2016 |
| OCT-angiography assessing quiescent and active choroidal neovascularization in retinitis pigmentosa associated with PRPH2 pathogenic variant Y Falfoul, KEL Matri, I Habibi, S Halouani, A Chebil, D Schorderet, ... European Journal of Ophthalmology 32 (4), NP98-NP102, 2022 | 8 | 2022 |
| Posterior staphylomas in non-highly myopic eyes with retinitis pigmentosa L El Matri, Y Falfoul, K El Matri, I El Euch, H Ghali, I Habibi, A Hassairi, ... International ophthalmology 40, 2159-2168, 2020 | 8 | 2020 |
| Novel PDE6B mutation presenting with retinitis pigmentosa–a case series of three patients A Palmowski-Wolfe, K Stingl, I Habibi, D Schorderet, HV Tran Klinische Monatsblätter für Augenheilkunde 236 (04), 562-567, 2019 | 6 | 2019 |
| Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations Y Falfoul, I Habibi, A Turki, A Chebil, A Hassairi, DF Schorderet, L El Matri Journal of ophthalmology 2018 (1), 1030184, 2018 | 6 | 2018 |
| Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families I Habibi, I Sfar, W Ben Alaya, J Methlouthi, A Ayadi, M Brahim, J Blouin, ... International Journal of Nephrology and Renovascular Disease, 85-92, 2010 | 6 | 2010 |
| Complement component C3 variant (R102G) and the risk of Neovascular age-related macular degeneration in a Tunisian population I Habibi, I Sfar, F Kort, R Bouraoui, A Chebil, R Limaiem, S Ayed, ... Klinische Monatsblätter für Augenheilkunde 234 (04), 478-482, 2017 | 5 | 2017 |
| Different phenotypes in pseudodominant inherited retinal dystrophies I Habibi, Y Falfoul, HV Tran, K El Matri, A Chebil, L El Matri, DF Schorderet Frontiers in Cell and Developmental Biology 9, 625560, 2021 | 4 | 2021 |
| Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia I Habibi, M Youssef, E Marzouk, N El Shakankiri, G Gawdat, M El Sada, ... Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 221-226, 2019 | 4 | 2019 |
