| 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 | 48 | 2009 |
| 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), 2016 | 23 | 2016 |
| 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 (4), 991-995, 2016 | 20 | 2016 |
| 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 (2), 225, 2009 | 18 | 2009 |
| 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 | 16 | 2018 |
| 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 | 16 | 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 | 16 | 2014 |
| 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 | 16 | 2012 |
| Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease M Khatami, MM Heidari, S Soheilyfar Archives of medical sciences. Atherosclerotic diseases 1 (1), e9, 2016 | 15 | 2016 |
| 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 | 14 | 2013 |
| Rapid Detection of Escherichia coli O157: H7 by Fluorescent Amplification–Based Specific Hybridization (FLASH) PCR F Khatami, M Heidari, M Khatami Iranian Red Crescent Medical Journal 14 (9), 594, 2012 | 12 | 2012 |
| Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor? M Khatami, M Houshmand, M Sadeghizadeh, M Eftekharzadeh, ... Cardiovascular Pathology 19 (2), e21-e27, 2010 | 12 | 2010 |
| Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich’s ataxia patients MM Heidari, M Houshmand, S Hosseinkhani, S Nafissi, ... Neurological Sciences 29 (6), 489-493, 2008 | 11 | 2008 |
| 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 | 8 | 2017 |
| 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 | 7 | 2019 |
| 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 | 7 | 2017 |
| Novel point mutations in frataxin gene in Iranian patients with Friedreich’s ataxia MM Heidari, M Khatami, J Pourakrami Iranian journal of child neurology 8 (1), 32, 2014 | 6 | 2014 |
| 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 | 5 | 2018 |
| Designing and validation of one-step T-ARMS-PCR for genotyping the eNOS rs1799983 SNP MM Heidar, M Khatami Iranian journal of biotechnology 15 (3), 208, 2017 | 5 | 2017 |
| Mutation analysis in exons 22 and 24 of SCN4A gene in Iranian patients with non-dystrophic myotonia MM Heidari, M Khatami, S Nafissi, F Hesami-Zokai, A Khorrami Iranian journal of neurology 14 (4), 190, 2015 | 5 | 2015 |
