| Kernel machine SNP set analysis finds the association of BUD13, ZPR1, and APOA5 variants with metabolic syndrome in Tehran Cardio-metabolic Genetics Study S Masjoudi, B Sedaghati-Khayat, NJ Givi, LNH Bonab, F Azizi, ... Scientific Reports 11 (1), 10305, 2021 | 14 | 2021 |
| Cohort profile update: Tehran cardiometabolic genetic study MS Daneshpour, M Akbarzadeh, H Lanjanian, B Sedaghati-Khayat, ... European Journal of Epidemiology 38 (6), 699-711, 2023 | 9 | 2023 |
| Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case–control study and meta-analysis M Moazzam-Jazi, L Najd-Hassan-Bonab, S Masjoudi, M Tohidi, ... Scientific Reports 12 (1), 20709, 2022 | 5 | 2022 |
| Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS) LNH Bonab, M Moazzam-Jazi, RSM Moosavi, MS Fallah, H Lanjanian, ... Gene 778, 145485, 2021 | 4 | 2021 |
| Sex, age, and ethnic dependency of lipoprotein variants as the risk factors of ischemic heart disease: a detailed study on the different age-classes and genders in Tehran … H Lanjanian, L Najd Hassan Bonab, M Akbarzadeh, M Moazzam-Jazi, ... Biology of sex Differences 13 (1), 4, 2022 | 3 | 2022 |
| Performance of Illumina Next Generation Sequencing MS Daneshpour, S Masjoodi, N Ghafari, M Raesi, MS Fallah Pathobiology Research 21 (3), 153-161, 2018 | 2 | 2018 |
| From Genes to Diagnosis: Examining the Clinical and Genetic Spectrum of Maturity-Onset Diabetes of the Young (MODY) in TCGS S Asgarian, H Lanjanian, SR Anaraki, F Hadaegh, M Moazzam-jazi, ... | 1 | 2024 |
| Sex-specific association of FABP2 polymorphisms with the risk of obesity in the Tehran Cardio-Metabolic Genetic Study (TCGS) L Najd-Hassan-Bonab, NJ Givi, M Moazzam-Jazi, S Masjoudi, N Ghafari, ... Gene 876, 147519, 2023 | 1 | 2023 |
| Chromosomal regions strongly associated with waist circumference and body mass index in metabolic syndrome in a family-based study MS Daneshpour, M Zarkesh, S Masjoudi, F Azizi, M Hedayati Scientific Reports 11 (1), 6082, 2021 | 1 | 2021 |
| The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes M Amiri Roudbar, SM Vahedi, J Jin, M Jahangiri, H Lanjanian, D Habibi, ... Human genomics 18 (1), 98, 2024 | | 2024 |
| Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran S Asgarian, H Lanjanian, S Rahimipour Anaraki, F Hadaegh, ... Scientific Reports 14 (1), 19860, 2024 | | 2024 |
| The Tehran longitudinal family-based cardiometabolic cohort study sheds new light on dyslipidemia transmission patterns M Akbarzadeh, P Riahi, AH Saeidian, M Zarkesh, S Masjoudi, S Asgarian, ... Scientific Reports 14 (1), 4739, 2024 | | 2024 |
| Causality of Genetically Determined Monounsaturated Fatty Acids on Risk of Cardiovascular Disease: A Mendelian Randomization Study M Mansourian, D Habibi, M Akbarzadeh, F Teymoori, ST Fateh, ... | | 2023 |
| Causality of Genetically Determined Monounsaturated Fatty Acids on Risk of Cardiovascular Disease: A Mendelian Randomization Study D Habibi, M Akbarzadeh, F Teymoori, ST Fateh, S Masjoudi, AH Saeidian, ... medRxiv, 2023.09. 06.23295142, 2023 | | 2023 |
| Application of whole-exome sequencing in daily practice: reducing the cost, diagnostic odyssey, increasing the diagnostic rate MS Fallah, MS Daneshpour, S Zeinali, H Bagherian, S Masjoudi, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1818-1818, 2019 | | 2019 |
| Next Generation Sequencing in Genome: Illumina Method MS Daneshpour, S Masjoodi, MS Fallah, P Eshraghi | | 2015 |
Maryam DaneshpourResearch Institute for Endocrine Science, Shahid Beheshti university of medical sciences在 sbmu.ac.ir 的电子邮件经过验证
