Habiba Chaabouni Bouhamed

Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families

Periklis Makrythanasis, Mari Nelis, Federico Santoni et al. · Human Mutation · 2014 · 85 citations

Array Cgh, Rare Diseases, Mendelian Disorder +15

Genetics and genomic medicine in Tunisia

Houda Elloumi‐Zghal, Habiba Chaabouni Bouhamed · Molecular Genetics & Genomic Medicine · 2018 · 23 citations · Full text

The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly

Manèl Chograni, Imen Rejeb, Lamia Ben Jemâa et al. · European Journal of Human Genetics · 2011 · 22 citations · Full text

Single-cell genetic analysis validates cytopathological identification of circulating cancer cells in patients with clear cell renal cell carcinoma

Lucile Broncy, Basma Ben Njima, Arnaud Méjean et al. · Oncotarget · 2018 · 22 citations · Full text