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Intissar Ezzidi
Affiliation : University of Monastir
- 32Publications (affiliation in Tunisia)
- 36Total publications
- 775Citations
- 15h-index
Research profile
Intissar Ezzidi has 32 indexed publications (2006–2025). Their work appears mainly in “Diabetes & Metabolism”, “Clinical Endocrinology” and “Life”. Their most cited article, “MTHFR C677T and A1298C gene polymorphisms and hyperhomocysteinemia as risk factors of diabetic nephropathy in type 2 diabetes patients” (2006), has been cited 108 times. 8 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in Saudi Arabia, United Kingdom.
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Create my free profile Add my publicationsResearch areas
- Genetic Associations and Epidemiology
- Ovarian function and disorders
- Chronic Kidney Disease and Diabetes
- Adipokines, Inflammation, and Metabolic Diseases
- Genetic and Kidney Cyst Diseases
Publications (32)
- The Role of AMH and AMHR2 Variants in Polycystic Ovary Syndrome: ‘A Comprehensive Analysis’
- A novel link between KCNQ1 genetic variants and polycystic ovary syndrome susceptibility
- ADIPOQ Variants rs1501299 and rs3774261 and Hypoadiponectinemia in Obese Women with PCOS: Genetic and Metabolic Interactions
- Association study between adiponectin gene variants, serum levels and the risk of type 2 diabetes in Tunisian women: Insights from BMI stratification
- Exploring the Association of Biochemical Characterization and Genetic Determinants of TNF-α, CXCR2, and CCR5 Delta 32 Mutation with Predisposition to Polycystic Ovary Syndrome
- Abstract #1869798 Exploring the Genetic Contribution of Interleukin-10 Variants to Polycystic Ovary Syndrome Susceptibility in a Tunisian Population: A Case-Control Study
- Association of matrix metalloproteinase‐2 gene variants with diabetic nephropathy risk
- Interleukin 10 (IL-10) gene variants and haplotypes in Tunisian women with polycystic ovary syndrome (PCOS): a case-control study
- Association of MMP-2 genes variants with diabetic retinopathy in Tunisian population with type 2 diabetes
- Adiponectin (ADIPOQ) gene variants and haplotypes in Saudi Arabian women with polycystic ovary syndrome (PCOS): a case–control study
- Impact of variants on type-2 diabetes risk genes identified through genomewide association studies in polycystic ovary syndrome: a case–control study
- Common polymorphisms of calpain-10 and the risk of polycystic ovary syndrome in Tunisian population: a case–control study
- European genetic variants associated with type 2 diabetes in North African Arabs
- Single-nucleotide polymorphisms and haplotypes in the adiponectin gene contribute to the genetic risk for type 2 diabetes in Tunisian Arabs
- Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes
- P231 Polymorphismes de l’Endothelial nitric oxide synthase Glu298Asp, 4b/a, and T-786C et la rétinopathie diabétique de type 2
- Renin–angiotensin–aldosterone system genotypes and haplotypes affect the susceptibility to nephropathy in type 2 diabetes patients
- P129 - Contribution des variants géniques du Calpain-10 au risque du diabète type 2 et les traits métaboliques reliés chez les Tunisiens arabes
- Association des polymorphismes du gène de la calpaïne 10 et d’un diabète de type 2 et traits métaboliques associés dans la population tunisienne
- Common polymorphisms of calpain-10 and the risk of Type 2 Diabetes in a Tunisian Arab population: a case-control study
- Variants within the calpain-10 gene and relationships with type 2 diabetes (T2DM) and T2DM-related traits among Tunisian Arabs
- Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study
- Identification of specific angiotensin‐converting enzyme variants and haplotypes that confer risk and protection against type 2 diabetic nephropathy
- Diabetic retinopathy, PAI-1 4G/5G and −844G/A polymorphisms, and changes in circulating PAI-1 levels in Tunisian type 2 diabetes patients
- P123 Polymorphismes -6754G/5G et -844G/A du gène du PAI-1 (Plasminogene Activator Inhibitor-1) chez les diabétiques de type 2, en Tunisie
- O95 Polymorphismes du gène de l’enzyme de conversion de l’angiotensine (ACE) et susceptibilité à la néphropathie chez les diabétiques de type 2 en Tunisie
- Association of endothelial nitric oxide synthase Glu298Asp, 4b/a, and −786T>C gene variants with diabetic nephropathy
- Interleukin‐10–592C/A, –819C/T and –1082A/G promoter variants affect the susceptibility to nephropathy in Tunisian type 2 diabetes (T2DM) patients
- Predictive value of interleukin‐10 promoter genotypes and haplotypes in determining the susceptibility to nephropathy in type 2 diabetes patients
- Endothelial nitric oxide synthase Glu298Asp, 4b/a, and T‐786C polymorphisms in type 2 diabetic retinopathy
- Association of the peroxisome proliferator-activated receptor-γ2 Pro12Ala but not the C1431T gene variants with lower body mass index in Type 2 diabetes
- MTHFR C677T and A1298C gene polymorphisms and hyperhomocysteinemia as risk factors of diabetic nephropathy in type 2 diabetes patients
Publication venues
- Diabetes & Metabolism × 7
- Clinical Endocrinology × 3
- Life × 2
- Molecular Biology Reports × 2
- Journal of Diabetes and its Complications × 2
- Diabetes Research and Clinical Practice × 2
Publications per year
- 20253
- 20243
- 20232
- 20221
- 20191
- 20181
- 20141
- 20124
- 20113
- 20102
Collaborations
Partner institutions : Hôpital Farhat Hached · University of Tabuk · Arabian Gulf University · Tunis El Manar University · Tunis University
Co-authors’ countries : Saudi Arabia · United Kingdom
Co-authors
- Nabil Mtiraoui
- Touhami Mahjoub
- Manel Ben Hadj Mohamed
- Sameh Sarray
- M. Kacem
- Assila Ben Salem
- Molka Chaieb
- Amira Turki
- T. Mahjoub
- Hassen Ben Abdennebi
- M. Chaïeb
- L. Chaïeb
Bibliographic data from OpenAlex (open database).
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