Accueil › Annuaire des chercheurs › Hamza Dallali
Hamza Dallali
Affiliation : University of Carthage · Institut Pasteur de Tunis · National Institute of Applied Science and Technology
- 35Publications (affiliation tunisienne)
- 52Publications au total
- 307Citations
- 11Indice h
Profil de recherche
Hamza Dallali compte 35 publications référencées (2017–2026). Ses travaux paraissent principalement dans « Frontiers in Genetics », « PLoS ONE » et « Bioscience Reports ». Son article le plus cité, « Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort » (2017), a été cité 28 fois. 7 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de France, Afrique du Sud.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Nutrition, Genetics, and Disease
- BRCA gene mutations in cancer
Publications (35)
- Metataxonomic strategy to decipher gut bacteriome biomarkers of type 2 diabetes and obesity in Tunisian population
- Genomic Insights into Unspecified Monogenic Forms of Diabetes and Their Associated Comorbidities: Implication for Treatment
- Hemoglobin Disorders Associated with Neurological Impairment: First Report of ATR-X Syndrome and Recessive Congenital Methemoglobinemia Type II in Tunisia
- Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
- Pharmacogenetic landscape of pain management variants among Mediterranean populations
- Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
- Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
- Decoding the genetic relationship between Alzheimer’s disease and type 2 diabetes: potential risk variants and future direction for North Africa
- Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare management
- The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetes
- PHINDaccess Hackathons for COVID‐19 and Host‐Pathogen Interaction: Lessons Learned and Recommendations for Low‐ and Middle‐Income Countries
- Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis
- Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
- Correction to: Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohort
- Multiallelic Rare Variants in BBS Genes Support an Oligogenic Ciliopathy in a Non-obese Juvenile-Onset Syndromic Diabetic Patient: A Case Report
- Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia
- Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital Ichthyosis
- A map of copy number variations in the Tunisian population: a valuable tool for medical genomics in North Africa
- Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
- Development of a custom next-generation sequencing panel for the determination of bladder cancer risk in a Tunisian cohort
- Development of a Custom NGS Panel for the Determination of Bladder Cancer Risk
- Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa
- Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young
- Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 Cases
- Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family
- Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
- Whole exome sequencing reveals a combination of rare high and low penetrance variants that correlates with familial breast cancer relative risk
- Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing
- Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
- Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome
- Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family
- Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations
- Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort
- Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis
- Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population
Revues de publication
- Frontiers in Genetics × 5
- PLoS ONE × 4
- Bioscience Reports × 3
- Molecular Biology Reports × 3
- Current Issues in Molecular Biology × 1
- International Journal of Molecular Sciences × 1
Publications par année
- 20261
- 20252
- 20244
- 20234
- 20223
- 20217
- 20206
- 20194
- 20181
- 20173
Collaborations
Établissements partenaires : Tunis El Manar University · Tunis University · Faculté de médecine de Tunis · Hôpital Charles-Nicolle · Institut National de Nutrition et de Technologie Alimentaire
Pays des co-auteurs : France · Afrique du Sud
Co-auteurs
- Sonia Abdelhak
- Rym Kéfi
- Meriem Hechmi
- Haifa Jmel
- Olfa Messaoud
- H. Jamoussi
- Abdelmajid Abid
- Yosr Hamdi
- Nadia Kheriji
- Lilia Romdhane
- Ridha Mrad
- Ismail Gouiza
Données bibliographiques issues d’OpenAlex (base ouverte).
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