| MicroRNAs: roles in cardiovascular development and disease S Kalayinia, F Arjmand, M Maleki, M Malakootian, CP Singh Cardiovascular Pathology 50, 107296, 2021 | 114 | 2021 |
| Next generation sequencing applications for cardiovascular disease S Kalayinia, H Goodarzynejad, M Maleki, N Mahdieh Annals of Medicine 50 (2), 91-109, 2018 | 45 | 2018 |
| The impact of vascular endothelial growth factor +405 C/G polymorphism on long-term outcome and severity of coronary artery disease S Kalayi Nia, S Ziaee, MA Boroumand, M Sotudeh Anvari, L Pourgholi, ... Journal of Clinical Laboratory Analysis 31 (4), 1-7, 2017 | 17 | 2017 |
| A novel de novo dominant mutation of NOTCH1 gene in an Iranian family with non‐syndromic congenital heart disease S Kalayinia, M Maleki, M Mahdavi, N Mahdieh Journal of Clinical Laboratory Analysis 34 (4), e23147, 2020 | 15 | 2020 |
| A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease S Kalayinia, S Ghasemi, N Mahdieh Journal of cardiovascular and thoracic research 11 (4), 287, 2019 | 12 | 2019 |
| Chromosome 9 inversion: pathogenic or benign? A comprehensive systematic review of all clinical reports N Mohsen-Pour, T Talebi, N Naderi, MH Moghadam, M Maleki, ... Current Molecular Medicine 22 (5), 385-400, 2022 | 11 | 2022 |
| Association between the atrial natriuretic peptide rs5065 gene polymorphism and the presence and severity of coronary artery disease in an Iranian population S Ziaee, S Kalayinia, MA Boroumand, L Pourgholi, S Cheraghi, MS Anvari, ... Coronary artery disease 25 (3), 242-246, 2014 | 11 | 2014 |
| 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 |
| Dilated cardiomyopathy caused by a pathogenic nucleotide variant in RBM20 in an Iranian family M Malakootian, M Bagheri Moghaddam, S Kalayinia, M Farrashi, ... BMC Medical Genomics 15 (1), 106, 2022 | 7 | 2022 |
| Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family M Mahdavi, N Mohsen-Pour, M Maleki, M Hesami, N Naderi, ... Cardiology in the Young 32 (9), 1462-1467, 2022 | 6 | 2022 |
| Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation M Malakootian, M Jalilian, S Kalayinia, M Hosseini Moghadam, ... BMC Cardiovascular Disorders 22 (1), 37, 2022 | 6 | 2022 |
| GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co‐occurrence of a novel de novo translocation (5;7) and a likely pathogenic … S Kalayinia, M Maleki, H Rokni‐Zadeh, M Changi‐Ashtiani, H Ahangar, ... Journal of Clinical Laboratory Analysis 33 (7), e22923, 2019 | 6 | 2019 |
| Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: a case report S Kalayinia, T Shahani, A Biglari, M Maleki, H Rokni‐Zadeh, Z Razavi, ... Journal of Clinical Laboratory Analysis 33 (2), e22663, 2019 | 6 | 2019 |
| Extracellular matrix protein 1 gene (ECM1) mutations in nine Iranian families with lipoid proteinosis F Izadi, F Mahjoubi, M Farhadi, S Kalayinia, A Bidmeshkipour, ... Indian Journal of Medical Research 143 (3), 303-307, 2016 | 6 | 2016 |
| Development of a patients’ satisfaction analysis system using machine learning and lexicon-based methods S Khaleghparast, M Maleki, G Hajianfar, E Soumari, M Oveisi, ... BMC Health Services Research 23 (1), 280, 2023 | 5 | 2023 |
| Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot S Kalayinia, M Maleki, M Mahdavi, N Mahdieh Laboratory Medicine 52 (6), 614-618, 2021 | 5 | 2021 |
| Hybrid Machine Learning Systems for Prediction of Parkinson’s Disease Pathogenic Variants Using Clinical Information and Radiomics Features G Hajianfar, S Kalayinia, M Hosseinzadeh, S Samanian, M Maleki, ... Journal of Nuclear Medicine 63 (supplement 2), 2508-2508, 2022 | 4 | 2022 |
| 9P21. 3 locus; An important region in coronary artery disease: a panel approach to investigation of the coronary artery disease etiology S Omidi, F Ebrahimzadeh, S Kalayinia International Journal of Cardiovascular Practice 4 (2), 21-35, 2019 | 4 | 2019 |
| The Nkx2-5 gene mutations related to congenital heart diseases in Iranian patients population S Kalayinia, A Biglari, H Rokni-Zadeh, M Mahdavi, B Rabbani, M Maleki, ... International Cardiovascular Research Journal 12 (3), 2018 | 4 | 2018 |
| The association between in vitro fertilization and intracytoplasmic sperm injection treatment and the risk of congenital heart defects T Talebi, N Mohsen-Pour, M Hesami, M Maleki, S Kalayinia The Journal of Maternal-Fetal & Neonatal Medicine 35 (25), 7471-7485, 2022 | 3 | 2022 |
