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Khaled Lasram
Affiliation : Institut Pasteur de Tunis
- 18Publications (affiliation in Tunisia)
- 22Total publications
- 431Citations
- 12h-index
Research profile
Khaled Lasram has 18 indexed publications (2012–2025). Their work appears mainly in “Mitochondrial DNA”, “Primary care diabetes” and “bioRxiv (Cold Spring Harbor Laboratory)”. Their most cited article, “Consanguinity, endogamy, and genetic disorders in Tunisia” (2012), has been cited 107 times. Their work is co-authored with at least 12 researchers, including institutions in India, France.
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Create my free profile Add my publicationsResearch areas
- Genetic Associations and Epidemiology
- Forensic and Genetic Research
- Genetic diversity and population structure
- Diabetes and associated disorders
- Mitochondrial Function and Pathology
Publications (18)
- Chronotherapy as a Potential Strategy to Reduce Ifosfamide-Induced Encephalopathy: A Preclinical Study in a Murine Model
- Mitochondrial DNA structure of an isolated Tunisian Berber population and its relationship with Mediterranean populations
- Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome
- Differential impact of consanguineous marriages on autosomal recessive diseases in T unisia
- Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population
- Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity
- Association Analysis of IGF2BP2, KCNJ11, and CDKAL1 Polymorphisms with Type 2 Diabetes Mellitus in a Moroccan Population: A Case–Control Study and Meta-analysis
- Phylogeny and genetic structure of Tunisians and their position within Mediterranean populations
- Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the T unisian population 在突尼斯人群中，CDKAL1 rs7756992与IGF2BP2 rs4402960的多态性对2型糖尿病、糖尿病并发症、肥胖风险以及高血压的影响
- Evidence for Association of the E23K Variant ofKCNJ11Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis
- Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean region
- E23K variant in KCNJ11 gene is associated with susceptibility to type 2 diabetes in the Mauritanian population
- Type 2 diabetes in Mauritania: Prevalence of the undiagnosed diabetes, influence of family history and maternal effect
- Association study of mitochondrial DNA polymorphisms with type 2 diabetes in Tunisian population
- Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III
- Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia
- mtDNA 16184–16193 poly-C tract does not predispose to type 2 diabetes in the Mauritanian population
- Consanguinity, endogamy, and genetic disorders in Tunisia
Publication venues
- Mitochondrial DNA × 2
- Primary care diabetes × 2
- bioRxiv (Cold Spring Harbor Laboratory) × 1
- Annals of Human Biology × 1
- Metabolic Syndrome and Related Disorders × 1
- American Journal of Human Biology × 1
Publications per year
- 20251
- 20181
- 20161
- 20153
- 20145
- 20136
- 20121
Collaborations
Partner institutions : Tunis El Manar University · Institut National de Nutrition et de Technologie Alimentaire · Tunis University · Faculté de médecine de Tunis · Hôpital La Rabta
Co-authors’ countries : India · France
Co-authors
- Sonia Abdelhak
- Rym Kéfi
- Nizar Ben Halim
- Sana Hsouna
- Lilia Romdhane
- Slim Ben Ammar
- Sonia Bahri
- H. Jamoussi
- Imen Arfa
- Abdelmajid Abid
- Majdi Nagara
- H. Abid
Bibliographic data from OpenAlex (open database).
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