HD
Hamza Dallali

Publications (16)

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Article scientifique · 2024
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Article scientifique · 2024
The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes
Article scientifique · 2023
Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare management
Article scientifique · 2023
Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis
Article scientifique · 2022
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Article scientifique · 2021
Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis
Article scientifique · 2021
Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case Report
Article scientifique · 2021
Development of a Custom NGS Panel for the Determination of Bladder Cancer Risk
Article scientifique · 2021
A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
Article scientifique · 2021
Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
Article scientifique · 2021
Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
Article scientifique · 2020
Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
Article scientifique · 2020
Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases
Article scientifique · 2020
Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations
Article scientifique · 2018
Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort
Article scientifique · 2017

Domaines principaux

Sciences de la santé8 Sciences de la vie et biotechnologies8

Statistiques

Consultations32
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