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Afef Slimani
Affiliation : Tunis University · Tunis El Manar University
- 18Publications (affiliation in Tunisia)
- 23Total publications
- 247Citations
- 11h-index
Research profile
Afef Slimani has 18 indexed publications (2010–2026). Their work appears mainly in “Journal of Molecular Neuroscience”, “Diagnostic Pathology” and “Clinica Chimica Acta”. Their most cited article, “Effect of E670G Polymorphism in PCSK9 Gene on the Risk and Severity of Coronary Heart Disease and Ischemic Stroke in a Tunisian Cohort” (2014), has been cited 52 times. 3 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Lipoproteins and Cardiovascular Health
- Genetic Associations and Epidemiology
- Lipid metabolism and disorders
- Paraoxonase enzyme and polymorphisms
- Peroxisome Proliferator-Activated Receptors
Publications (18)
- Dynamic Risk-Aware Attack Path Prioritization using Dynamic Node Risk Modeling
- SHFL-EI: Secure Hierarchical Federated Learning with Edge Intelligence for Robust IoT Security
- The association between Dental Fluorosis and COL1A2 gene polymorphism among a Tunisian Population
- Diabète de type 2 et proprotein convertase subtilisin/kexin type 9 : y-a-t-il un lien ?
- AGT M235t polymorphism and heart failure in a cohort of Tunisian population: diagnostic and prognostic value.
- Effect of E670G Polymorphism in PCSK9 Gene on the Risk and Severity of Coronary Heart Disease and Ischemic Stroke in a Tunisian Cohort
- PCSK9 polymorphism in a Tunisian cohort: Identification of a new allele, L8, and association of allele L10 with reduced coronary heart disease risk
- Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene
- A Pro 12 Ala substitution in the PPARγ2 polymorphism may decrease the number of diseased vessels and the severity of angiographic coronary artery
- Combined Effects of the C161T and Pro12Ala PPARγ2 Gene Variants with Insulin Resistance on Metabolic Syndrome: A Case–Control Study of a Central Tunisian Population
- Interaction Effects of the Leu162Val PPARαand Pro12Ala PPARγ2 Gene Variants with Renal Function in Metabolic Syndrome Population
- Autosomal Dominant Hypercholesterolemia: Needs for Early Diagnosis and Cascade Screening in the Tunisian Population
- Effect of mutations in LDLR and PCSK9 genes on phenotypic variability in Tunisian familial hypercholesterolemia patients
- Hsp70-2 gene polymorphism: susceptibility implication in Tunisian patients with coronary artery disease
- Genomic characterization of two deletions in the LDLR gene in Tunisian patients with familial hypercholesterolemia
- Association entre des variations de la lipoprotéine lipase et la maladie coronarienne dans une population tunisienne
- +294T/C polymorphism in the PPAR-δ gene is associated with risk of coronary artery disease in normolipidemic Tunisians
- Moderate phenotypic expression of familial hypercholesterolemia in Tunisia
Publication venues
- Journal of Molecular Neuroscience × 2
- Diagnostic Pathology × 2
- Clinica Chimica Acta × 2
- SSRN Electronic Journal × 1
- International Symposium on Networks, Computers and Communications (ISNCC) × 1
- BMC Oral Health × 1
Publications per year
- 20262
- 20241
- 20201
- 20151
- 20142
- 20135
- 20123
- 20111
- 20102
Collaborations
Partner institutions : University of Monastir · Hospital Fatuma Bourguiba Monastir · Hôpital Farhat Hached · Hôpital Sahloul · National Institute of Applied Science and Technology
Co-authors
- Mohamed Najah
- Mohamed Naceur Slimane
- Awatef Jelassi
- Khaldoun Ben Hamda
- Faouzi Maatouk
- Imen Jguirim
- Sarraj Mohamed Youssef
- Faouzi Addad
- Najjar Mohamed Fadhel
- Mohamed Yahia Hrira
- Ben Hamda Khaldoun
- Imen Trabelsi
Bibliographic data from OpenAlex (open database).
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