I. Lariani

Mutation spectrum and prevalence of <i>BRCA</i>1 and <i>BRCA</i>2 genes in patients with familial and early‐onset breast/ovarian cancer from Tunisia

Aouatef Riahi, Maher Kharrat, Mohamed El Ghourabi et al. · Clinical Genetics · 2013 · 48 citations

Breast Oncology, Cancer Pathology, Brca1/brca2 Mutations +17

Autosomal recessive congenital cataract, intellectual disability phenotype linked to <i><scp>STX3</scp></i> in a consanguineous Tunisian family

Manèl Chograni, Fowzan S. Alkuraya, I. Ourteni et al. · Clinical Genetics · 2014 · 14 citations

RGS6: A Novel Gene Associated With Congenital Cataract, Mental Retardation, and Microcephaly in a Tunisian Family

Manèl Chograni, Fowzan S. Alkuraya, Faouzi Mâazoul et al. · Investigative Ophthalmology & Visual Science · 2014 · 13 citations

High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families

Aouatef Riahi, Maher Kharrat, I. Lariani et al. · Familial Cancer · 2014 · 12 citations

Breast Oncology, Oncology, Somatic Variant +10