| The outbreak of the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): A review of the current global status M Bchetnia, C Girard, C Duchaine, C Laprise Journal of infection and public health 13 (11), 1601-1610, 2020 | 244 | 2020 |
| Clinical and mutational heterogeneity of Darier disease in Tunisian families M Bchetnia, C Charfeddine, S Kassar, H Zribi, HT Guettiti, F Ellouze, ... Archives of Dermatology 145 (6), 654-656, 2009 | 47 | 2009 |
| Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean region M Bchetnia, N Laroussi, M Youssef, C Charfeddine, AS Ben Brick, ... BioMed Research International 2013 (1), 206803, 2013 | 27 | 2013 |
| Expression signature of epidermolysis bullosa simplex M Bchetnia, ML Tremblay, G Leclerc, A Dupérée, J Powell, C McCuaig, ... Human genetics 131, 393-406, 2012 | 26 | 2012 |
| Immunohistological study of involucrin expression in Darier's disease skin S Kassar, C Charfeddine, H Zribi, H Tounsi‐Kettiti, M Bchetnia, E Jerbi, ... Journal of cutaneous pathology 35 (7), 635-640, 2008 | 24 | 2008 |
| Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability M Bchetnia, L Bouchard, J Mathieu, PM Campeau, C Morin, D Brisson, ... Journal of Medical Genetics 58 (10), 653-665, 2021 | 23 | 2021 |
| Hailey‐Hailey disease in Tunisia R Benmously‐Mlika, M Bchetnia, S Deghais, SA Ben Brick, ... International journal of dermatology 49 (4), 396-401, 2010 | 21 | 2010 |
| Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports M Bchetnia, A Merdassi, C Charfeddine, F Mgaieth, S Kassar, F Ouechtati, ... Journal of medical case reports 4, 1-4, 2010 | 20 | 2010 |
| Histological characterization of Darier's disease in Tunisian families S Kassar, H Tounsi‐Kettiti, C Charfeddine, H Zribi, M Bchetnia, E Jerbi, ... Journal of the European Academy of Dermatology and Venereology 23 (10), 1178 …, 2009 | 15 | 2009 |
| Clinical and genetic investigation of atrial septal defect with atrioventricular conduction defect in a large consanguineous Tunisian family S Nouira, I Kamoun, H Ouragini, C Charfeddine, H Mahjoub, F Ouechtati, ... Archives of medical research 39 (4), 429-433, 2008 | 14 | 2008 |
| The first Mal de Meleda case in Libya: identification of a SLURP1 mutation. M Bchetnia, M Bozgia, N Laroussi, AS Ben Brick, C Charfeddine, ... International Journal of Dermatology 54 (12), 2015 | 11 | 2015 |
| New mutations of Darier disease in Tunisian patients M Bchetnia, R Benmously, AS Ben Brick, C Charfeddine, Y Ben Ameur, ... Archives of dermatological research 301, 615-619, 2009 | 10 | 2009 |
| Clinical, histological and genetic investigation of Buschke–Fischer–Brauer's disease in Tunisian families M Bchetnia, C Charfeddine, S Kassar, I Hanchi, H Tounsi-Guettiti, A Rebai, ... Journal of dermatological science 54 (1), 54-56, 2009 | 10 | 2009 |
| Clinical and molecular investigation of Buschke‐Fischer‐Brauer in consanguineous Tunisian families C Charfeddine, C Ktaifi, N Laroussi, H Hammami, H Jmel, Z Landoulsi, ... Journal of the European Academy of Dermatology and Venereology 30 (12), 2122 …, 2016 | 8 | 2016 |
| Reduction of keratin aggregates in epidermolysis bullosa simplex keratinocytes after pretreatment with trimethylamine N-oxide M Bchetnia, J Lacroix, T Farez, M Larouche, J Powell, C McCuaig, ... Experimental dermatology 25 (3), 229-230, 2015 | 8 | 2015 |
| Allele-specific inactivation of an autosomal dominant epidermolysis Bullosa simplex mutation using CRISPR-Cas9 M Bchetnia, R Dionne Gagne, J Powell, C Morin, C McCuaig, A Dupérée, ... The CRISPR Journal 5 (4), 586-597, 2022 | 7 | 2022 |
| Expression signature of the Leigh syndrome French-Canadian type M Bchetnia, J Tardif, C Morin, C Laprise Molecular Genetics and Metabolism Reports 30, 100847, 2022 | 7 | 2022 |
| Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia AS Ben Brick, N Laroussi, H Mesrati, R Kefi, M Bchetnia, K Lasram, ... Archives of dermatological research 306, 405-411, 2014 | 6 | 2014 |
| Gene expression analysis of epidermolysis bullosa simplex with mottled pigmentation M Bchetnia, T Farez, J Lacroix, G Leclerc, J Powell, C McCuaig, ... Journal of Dermatological Science 69 (1), 80-82, 2013 | 5 | 2013 |
| Severe epidermolysis bullosa simplex phenotype caused by codominant mutations p. Ile377Thr in keratin 14 and p. Gly138Glu in keratin 5 M Bchetnia, JP Allard, AM Boucher‐Lafleur, T Cruz Marino, A Dupéré, ... Experimental Dermatology 29 (10), 961-969, 2020 | 4 | 2020 |
