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Heliyon|November 13, 2023
An optimized method for PCR-based genotyping to detect human APOE polymorphismsLeila Najd-Hassan-Bonab, Mehdi Hedayati, Seyed Abolhassan Shahzadeh Fazeli, et al.
Scientific Reports|August 21, 2020
High genetic burden of type 2 diabetes can promote the high prevalence of disease: a longitudinal cohort study in IranMaryam Moazzam-Jazi, Leila Najd Hassan Bonab, Asiyeh Sadat Zahedi, et al.
Eating and Weight Disorders : EWD|November 26, 2022
The role of FTO variant rs1421085 in the relationship with obesity: a systematic review and meta-analysisLeila Najd-Hassan-Bonab, Mahdi Safarpour, Maryam Moazzam-Jazi, et al.
Cardiovascular Toxicology|August 4, 2025
Ancestry- and Age-Dependent Effects of NOS3 Polymorphisms on Coronary Heart Disease Risk: A Meta-analysisSaeideh Jafarinejad-Farsangi, Sara Asgarian, Sara Ghahari, et al.
BMC Endocrine Disorders|October 9, 2023
Association of rs2282679 polymorphism in vitamin D binding protein gene (GC) with the risk of vitamin D deficiency in an iranian population: season-specific vitamin D statusGolaleh Asghari, Emad Yuzbashian, Leila Najd-Hassan-Bonab, et al.
Journal of Diabetes and Metabolic Disorders|January 13, 2025
Association of resistin rs1862513, rs10401670 and rs3745367 polymorphisms with resistin level and insulin resistance in an Iranian type 2 diabetic populationMehdi Hedayati, Masoumeh Nezhadali, Helma Karimi, et al.
Nucleosides, Nucleotides & Nucleic Acids|May 23, 2024
The role of rs2236242 at SERPINA12 gene and vaspin level on papillary thyroid carcinomaSahar Torki, Masoumeh Nezhadali, Mehdi Hedayati, et al.
BMC Cardiovascular Disorders|June 13, 2026
Sex-stratified polygenic risk scores for coronary artery disease incidence: Insights from a 20-year cohort studyLeila Najd-Hassan-Bonab, Maryam Moazzam-Jazi, Davood Khalili, et al.
Gene|June 1, 2023
Sex-specific association of FABP2 polymorphisms with the risk of obesity in the Tehran Cardio-Metabolic Genetic Study (TCGS)Leila Najd-Hassan-Bonab, Niloufar Javanrouh Givi, Maryam Moazzam-Jazi, et al.
Scientific Reports|May 14, 2021
Kernel machine SNP set analysis finds the association of BUD13, ZPR1, and APOA5 variants with metabolic syndrome in Tehran Cardio-metabolic Genetics StudySajedeh Masjoudi, Bahareh Sedaghati-Khayat, Niloufar Javanrouh Givi, et al.
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