Simple and label-free electrochemical impedance Amelogenin gene hybridization biosensing based on reduced graphene oxide A Benvidi, N Rajabzadeh, M Mazloum-Ardakani, MM Heidari, ... Biosensors and Bioelectronics 58, 145-152, 2014 | 89 | 2014 |
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 | 68 | 2009 |
Inheritance examples of algebraic hyperstructures B Davvaz, AD Nezhad, MM Heidari Information Sciences 224, 180-187, 2013 | 67 | 2013 |
Comparison of impedimetric detection of DNA hybridization on chemically and electrochemically functionalized multi-wall carbon nanotubes modified electrode A Benvidi, N Rajabzadeh, M Mazloum-Ardakani, MM Heidari Sensors and Actuators B: Chemical 207, 673-682, 2015 | 49 | 2015 |
Simple and label-free detection of DNA hybridization on a modified graphene nanosheets electrode A Benvidi, N Rajabzadeh, HM Zahedi, M Mazloum-Ardakani, MM Heidari, ... Talanta 137, 80-86, 2015 | 45 | 2015 |
Carbamylated erythropoietin increases frataxin independent from the erythropoietin receptor B Sturm, M Helminger, H Steinkellner, MM Heidari, H Goldenberg, ... European journal of clinical investigation 40 (6), 561-565, 2010 | 45 | 2010 |
Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease M Khatami, MM Heidari Arch Med Sci 1, e9–e15, 2016 | 44 | 2016 |
Sex determination based on amelogenin DNA by modified electrode with gold nanoparticle M Mazloum-Ardakani, N Rajabzadeh, A Benvidi, MM Heidari Analytical biochemistry 443 (2), 132-138, 2013 | 36 | 2013 |
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 | 35 | 2016 |
Mitochondrial genetic variation in Iranian infertile men with varicocele MM Heidari, M Khatami, A Danafar, T Dianat, G Farahmand, AR Talebi Int J Fertil Steril (IJFS) 10 (3), 303-309, 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 | 30 | 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 | 30 | 2016 |
Development of One-Step Tetra-primer ARMS-PCR for Simultaneous Detection of the Angiotensin Converting Enzyme (ACE) I/D and rs4343 Gene Polymorphisms and the Correlation with … MM Heidari, M Hadadzadeh, H Fallahzadeh Avicenna Journal of Medical Biotechnology 11 (1), 118-123, 2019 | 27 | 2019 |
Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease MM Heidari, FS Mirfakhradini, F Tayefi, S Gorbani, M Khatami, ... Applied Biochemistry and Biotechnology 191, 1326–1339, 2020 | 23 | 2020 |
Mutation analysis of TNP1 gene in infertile men with varicocele MM Heidari, M Khatami, AR Talebi, M Fahime Iran J Reprod Med 12, 2014 | 23 | 2014 |
Polymorphisms of sperm protamine genes and CMA3 staining in infertile men with varicocele M Nayeri, AR Talebi, MM Heidari, SM Seifati, N Tabibnejad Revista internacional de andrologia 18 (1), 7-13, 2020 | 21 | 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 |
Synthesis, Structure Characterization, DNA Binding, and Cleavage Properties of Mononuclear and Tetranuclear Cluster of Copper(II) Complexes R Vafazadeh, N Hasanzade, MM Heidari, AC Willis Acta Chim. Slov. 62, 122–129, 2015 | 20 | 2015 |
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 | 20 | 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 | 19 | 2020 |