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BRCA1 and BRCA2 Germline Mutation Analysis in Hereditary Breast/Ovarian Cancer Families from the Aures Region (Eastern Algeria): First Report

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  1. Article

    Correction to: BRCA1 and BRCA2 Germline Mutation Analysis in Hereditary Breast/Ovarian Cancer Families from the Aures Region (Eastern Algeria): First Report

    The original version of this article unfortunately contained an error in the abstract section and Figure 2h image.

    Chiraz Mehemmai, Farid Cherbal, Yosr Hamdi… in Pathology & Oncology Research (2020)

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  2. Article

    Open Access

    Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins

    Lynch syndrome (LS) is a highly penetrant inherited cancer predisposition syndrome, characterized by autosomal dominant inheritance and germline mutations in DNA mismatch repair genes. Despite several genetic ...

    Amira Jaballah-Gabteni, Haifa Tounsi, Maria Kabbage… in Journal of Translational Medicine (2019)

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  3. Article

    Open Access

    A genome wide SNP genoty** study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci

    Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels of risk and prevalence. The ...

    Yosr Hamdi, Mariem Ben Rekaya, Shan **gxuan, Majdi Nagara, Olfa Messaoud… in BMC Cancer (2018)

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  4. Article

    Open Access

    Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases

    A family history of breast cancer has long been thought to indicate the presence of inherited genetic events that predispose to this disease. In North Africa, many specific epidemio-genetic characteristics hav...

    Yosr Hamdi, Maroua Boujemaa, Mariem Ben Rekaya… in Journal of Translational Medicine (2018)

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