17 Dec 2025Open access
Genomic Insights into Unspecified Monogenic Forms of Diabetes and Their Associated Comorbidities: Implication for TreatmentPublisher siteCurrent Issues in Molecular Biology, Genomics and Rare Diseases
UniversitiesHamza Dallali
Active, last published 2026
In pancreatic function and diabetes
Hamza
Dallali
Scholar“Research focused on Pancreatic function and diabetes and adjacent fields.”
Institut Pasteur de Tunis
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01 · About the work
What I study
amza Dallali is a researcher working on Pancreatic function and diabetes. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Hamza's work has been cited 301 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Pancreatic function and diabetes×6Genetic factors in colorectal cancer×6Cancer Genomics and Diagnostics×5Genetic Associations and Epidemiology×3Epigenetics and DNA Methylation×3
04 · Where I am
Affiliations
Affiliation on published researchInstitut Pasteur de TunisDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
10 works16 May 2025Open access
Hemoglobin Disorders Associated with Neurological Impairment: First Report of ATR-X Syndrome and Recessive Congenital Methemoglobinemia Type II in TunisiaPublisher siteInternational Journal of Molecular Sciences, Neonatal Health and Biochemistry
25 Jun 2024Open access1cites
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthPublisher siteFrontiers in Genetics, Hearing, Cochlea, Tinnitus, Genetics
15 May 2024Open access1cites
Pharmacogenetic landscape of pain management variants among Mediterranean populationsPublisher siteFrontiers in Pharmacology, Genetic Associations and Epidemiology
22 Apr 2024Open access1cites
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory healthPublisher siteFrontiers in Genetics, Hearing, Cochlea, Tinnitus, Genetics
12 Jan 2024Open access3cites
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencingPublisher siteFrontiers in Genetics, Mitochondrial Function and Pathology
19 Dec 2023Open access3cites
The first exome wide association study in Tunisia: identification of candidate loci and pathways with biological relevance for type 2 diabetesPublisher siteFrontiers in Endocrinology, Genetic Associations and Epidemiology
14 Dec 2023Open access3cites
Whole-exome sequencing reveals novel variants of monogenic diabetes in Tunisia: impact on diagnosis and healthcare managementPublisher siteFrontiers in Genetics, Genomics and Rare Diseases
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