| PPARG (Pro12Ala) genetic variant and risk of T2DM: a systematic review and meta-analysis N Sarhangi, F Sharifi, L Hashemian, M Hassani Doabsari, K Heshmatzad, ... Scientific reports 10 (1), 12764, 2020 | 66 | 2020 |
| The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel Variants K Heshmatzad, N Mahdieh, A Rabbani, A Didban, B Rabbani International journal of endocrinology 2020 (1), 2190508, 2020 | 8 | 2020 |
| Role of non‐coding variants in cardiovascular disease K Heshmatzad, N Naderi, M Maleki, S Abbasi, S Ghasemi, N Ashrafi, ... Journal of Cellular and Molecular Medicine 27 (12), 1621-1636, 2023 | 7 | 2023 |
| A systematic review of LDLR, PCSK9, and APOB variants in Asia N Mahdieh, K Heshmatzad, B Rabbani Atherosclerosis 305, 50-57, 2020 | 7 | 2020 |
| GFAP variants leading to infantile Alexander disease: Phenotype and genotype analysis of 135 cases and report of a de novo variant K Heshmatzad, MH Panah, AR Tavasoli, MR Ashrafi, N Mahdieh, ... Clinical Neurology and Neurosurgery 207, 106754, 2021 | 4 | 2021 |
| Effects of morphine and NeuroAid on the expression levels of GluN2A and GluN3A in the hippocampus and striatum of rats K Heshmatzad, M Nasehi, S Vaseghi Iranian Journal of Basic Medical Sciences 24 (4), 469, 2021 | 3 | 2021 |
| Genetic Variations in the Human Angiotensin-Converting Enzyme 2 and Susceptibility to Coronavirus Disease-19 T Talebi, T Masoumi, K Heshmatzad, M Hesami, M Maleki, S Kalayinia, ... Genetics Research 2023, e36, 2023 | 2 | 2023 |
| Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing K Heshmatzad, N Naderi, T Masoumi, H Pouraliakbar, S Kalayinia European Journal of Medical Research 27 (1), 174, 2022 | 1 | 2022 |
| Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population G Houshmand, MJ Alemzadeh-Ansari, S Mazloumzadeh, N Naderi, ... Journal of Cardiovascular and Thoracic Research 15 (3), 168, 2023 | | 2023 |
