Inès Ouertani

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

Claire Redin, Stéphanie Le Gras, O. M'hamdi et al. · Journal of Medical Genetics · 2012 · 113 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

Marie‐Pierre Audrézet, Christine Corbiere, Saïd Lebbah et al. · Journal of the American Society of Nephrology · 2015 · 85 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis

O. M'hamdi, Claire Redin, Corinne Stoetzel et al. · Clinical Genetics · 2013 · 31 citations

Life Sciences, Genetics, Molecular Genetics +16

Prevalence of Bardet–Biedl syndrome in Tunisia

Oussama M’Hamdi, Inès Ouertani, Faouzi Mâazoul et al. · Journal of Community Genetics · 2011 · 25 citations

Life Sciences, Cardiology, Human Genetics +1

WDR73-related galloway mowat syndrome with collapsing glomerulopathy

Mariem El Younsi, Lilia Kraoua, Rym Meddeb et al. · European Journal of Medical Genetics · 2018 · 13 citations

Medicine, Nephrology, Pathology +11