| Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxia MM Heidari, M Houshmand, S Hosseinkhani, S Nafissi, M Khatami Canadian journal of neurological sciences 36 (1), 26-31, 2009 | 67 | 2009 |
| Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease M Khatami, MM Heidari Archives of Medical Science-Atherosclerotic Diseases 1 (1), 9-15, 2016 | 45 | 2016 |
| Mitochondrial genetic variation in Iranian infertile men with varicocele MM Heidari, M Khatami, A Danafar, T Dianat, G Farahmand, AR Talebi International journal of fertility & sterility 10 (3), 303, 2016 | 34 | 2016 |
| Polymorphisms in NOS3, MTHFR, APOB and TNF-α genes and risk of coronary atherosclerotic lesions in Iranian patients MM Heidari, M Khatami, M Hadadzadeh, M Kazemi, S Mahamed, ... Research in cardiovascular medicine 5 (1), 1-6, 2016 | 34 | 2016 |
| Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome M FallahTafti, M Khatami, S Rezaei, MM Heidari, M Hadadzadeh Cardiology Journal 25 (1), 113–119, 2018 | 29 | 2018 |
| Upregulation of miR-222 in both Helicobacter pylori-infected and noninfected gastric cancer patients M Noormohammad, S Sadeghi, H Tabatabaeian, K Ghaedi, A Talebi, ... Journal of genetics 95, 991-995, 2016 | 28 | 2016 |
| Mutation analysis of TNP1 gene in infertile men with varicocele MM Heidari, M Khatami, AR Talebi, F Moezzi Iranian journal of reproductive medicine 12 (4), 257, 2014 | 24 | 2014 |
| Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease MM Heidari, FS Mirfakhradini, F Tayefi, S Ghorbani, M Khatami, ... Applied biochemistry and biotechnology 191 (3), 1326-1339, 2020 | 22 | 2020 |
| The POLG gene polymorphism in Iranian varicocele-associated infertility patients MM Heidari, M Khatami, AR Talebi Iranian journal of basic medical sciences 15 (2), 739, 2012 | 21 | 2012 |
| Relationship of the MTHFD1 (rs2236225), eNOS (rs1799983), CBS (rs2850144) and ACE (rs4343) gene polymorphisms in a population of Iranian pediatric patients with congenital … M Khatami, FM Ratki, S Tajfar, F Akrami The Kaohsiung journal of medical sciences 33 (9), 442-448, 2017 | 20 | 2017 |
| Protective effect of Berberis vulgaris on Fenton reaction-induced DNA cleavage NS Asadi, MM Heidari, M Khatami Avicenna journal of phytomedicine 9 (3), 213, 2019 | 19 | 2019 |
| Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis MM Heidari, M Khatami, Y Tahamtan Basic and Clinical Neuroscience 8 (4), 279-284, 2017 | 19 | 2017 |
| Simultaneous Genotyping of the Rs4762 and Rs699 Polymor-phisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR Khatami M, Heidari M, Hadadzadeh M, Schiber-Mojdehkar B, Bitaraf Sani M ... Iranian Journal of Public Health 46 (6), 811-819, 2017 | 19 | 2017 |
| A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich’s ataxia MM Heidari, M Houshmand, S Hosseinkhani, S Nafissi, ... Cellular and molecular neurobiology 29, 225-233, 2009 | 19 | 2009 |
| Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients S Dianatpour, M Khatami, MM Heidari, M Hadadzadeh Applied Biochemistry and Biotechnology 190, 896–906, 2020 | 18 | 2020 |
| The association of renin–angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss MM Heidari, M Sheikholeslami, M Yavari, M Khatami, SM Seyedhassani Human Fertility 22 (3), 164-170, 2019 | 18 | 2019 |
| Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease M Khatami, M Mazidi, S Taher, MM Heidari, M Hadadzadeh Medicina 53 (3), 1-11, 2018 | 18 | 2018 |
| Apolipoprotein E gene polymorphism in Iranian coronary atherosclerosis patients candidate for coronary artery bypass graft MM Heidari, SK Foruzannia, M Khatami, M Hadadzadeh, ME Meybodi Iranian journal of basic medical sciences 16 (7), 841, 2013 | 18 | 2013 |
| Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous … F Ghadamyari, MM Heidari, S Zeinali, M Khatami, S Merat, H Bagherian, ... Journal of Clinical Laboratory Analysis 35 (5), e23768, 2021 | 16 | 2021 |
| Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects M Khatami, MM Heidari, F Kazeminasab, R Zare Bidaki J Cardiovasc Thorac Res. 10 (1), 41-45, 2018 | 15 | 2018 |
