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Cancer in Africa: The Untold Story

Frontiers in oncology, 2021-04, Vol.11, p.650117

2021

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Genetic diversity of variants involved in drug response among Tunisian and Italian populations toward personalized medicine

Scientific reports, 2024-03, Vol.14 (1), p.5842-5842, Article 5842

2024

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Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticity

Scientific reports, 2024-02, Vol.14 (1), p.4654-4654, Article 4654

2024

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Health influenced by genetics: A first comprehensive analysis of breast cancer high and moderate penetrance susceptibility genes in the Tunisian population

PloS one, 2022-03, Vol.17 (3), p.e0265638-e0265638

2022

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Association between epidemiological and clinico-pathological features of breast cancer with prognosis, family history, Ki-67 proliferation index and survival in Tunisian breast cancer patients

PloS one, 2022-09, Vol.17 (9), p.e0269732-e0269732

2022

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Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia

PloS one, 2021-01, Vol.16 (1), p.e0245362-e0245362

2021

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Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East

Orphanet journal of rare diseases, 2012-08, Vol.7 (1), p.52-52, Article 52

2012

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Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis

PloS one, 2021-10, Vol.16 (10), p.e0258777-e0258777

2021

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

Pathology oncology research, 2020-04, Vol.26 (2), p.715-726

2020

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Prevalence and risk factors of diabetes mellitus and hypertension in North East Tunisia calling for efficient and effective actions

Scientific reports, 2023-08, Vol.13 (1), p.12706-12706, Article 12706

2023

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Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis

PloS one, 2021-10, Vol.16 (10)

2021

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Inflammatory landscape in Xeroderma pigmentosum patients with cutaneous melanoma

Scientific reports, 2022-08, Vol.12 (1), p.13854-13, Article 13854

2022

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High-quality genome sequence assembly of R.A73 Enterococcus faecium isolated from freshwater fish mucus

BMC microbiology, 2020-10, Vol.20 (1), p.322-12, Article 322

2020

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Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations

Orphanet journal of rare diseases, 2022-03, Vol.17 (1), p.121-121, Article 121

2022

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Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family

Journal of human genetics, 2020-04, Vol.65 (4), p.397-410

2020

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Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians

Breast cancer research and treatment, 2012-10, Vol.135 (3), p.715-724

2012

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Uncovering the clinical relevance of unclassified variants in DNA repair genes: a focus on BRCA negative Tunisian cancer families

Frontiers in genetics, 2024, Vol.15, p.1327894-1327894

2024

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Identification of two variants in AGRN and RPL3L genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance

Clinical case reports, 2022-02, Vol.10 (2), p.e05339-n/a

2022

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

Journal of translational medicine, 2018-06, Vol.16 (1), p.158-13, Article 158

2018

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Dysregulated PDGFR alpha expression and novel somatic mutations in colorectal cancer: association to RAS wild type status and tumor size

Journal of translational medicine, 2020-11, Vol.18 (1), p.440-440, Article 440

2020

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

BMC cancer, 2018-12, Vol.18 (1), p.1295-1295, Article 1295

2018

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Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations

PloS one, 2018-04, Vol.13 (4), p.e0194842-e0194842

2018

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Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young

Herz, 2021-04, Vol.46 (Suppl 1), p.94-102

2021

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Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case Report

Frontiers in genetics, 2021-10, Vol.12, p.664963

2021

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Cancer in Africa: The Untold Story

Genetic diversity of variants involved in drug response among Tunisian and Italian populations toward personalized medicine

Ethnic and functional differentiation of copy number polymorphisms in Tunisian and HapMap population unveils insights on genome organizational plasticity

Health influenced by genetics: A first comprehensive analysis of breast cancer high and moderate penetrance susceptibility genes in the Tunisian population

Association between epidemiological and clinico-pathological features of breast cancer with prognosis, family history, Ki-67 proliferation index and survival in Tunisian breast cancer patients

Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia

Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East

Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis

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

Prevalence and risk factors of diabetes mellitus and hypertension in North East Tunisia calling for efficient and effective actions

Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis

Inflammatory landscape in Xeroderma pigmentosum patients with cutaneous melanoma

High-quality genome sequence assembly of R.A73 Enterococcus faecium isolated from freshwater fish mucus

Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations

Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family

Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

Uncovering the clinical relevance of unclassified variants in DNA repair genes: a focus on BRCA negative Tunisian cancer families

Identification of two variants in AGRN and RPL3L genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance

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

Dysregulated PDGFR alpha expression and novel somatic mutations in colorectal cancer: association to RAS wild type status and tumor size

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

Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations

Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young

Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case Report

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