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Mohammad Mehdi Heidari
Mohammad Mehdi Heidari
Associate Professor of Molecular Genetics, Yazd University
Verified email at yazd.ac.ir
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Cited by
Cited by
Year
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
842014
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
652009
Inheritance examples of algebraic hyperstructures
B Davvaz, AD Nezhad, MM Heidari
Information Sciences 224, 180-187, 2013
632013
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
482015
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
432015
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
432010
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
402016
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
332016
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
332013
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
322016
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
272018
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
272016
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
252019
Mutation analysis of TNP1 gene in infertile men with varicocele
MM Heidari, M Khatami, AR Talebi, M Fahime
Iran J Reprod Med 12, 2014
232014
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
202020
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
202015
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
202012
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
192020
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
192013
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
192009
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