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Mehri Khatami

Observed names: Khatami, Mehri, M Khatami, M. Khatami, MEHRI KHATAMI
Institution: Yazd University
ORCID: 0000-0002-5840-5399
Observed ORCID: 0000-0002-5840-5399
OpenAlex ID: A5091592260
Complex I and ATP Content Deficiency in Lymphocytes from Friedreich's Ataxia
2009 · Mohammad Mehdi Heidari, Massoud Houshmand, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 55
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Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease
2016 · Mehri Khatami, Mohammad Mehdi Heidari, et al. · Archives of Medical Science - Atherosclerotic Diseases · 38
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Heterobimetallic PtII‐AuI Complexes Comprising Unsymmetrical 1,1‐Bis(diphenylphosphanyl)methane Bridges: Synthesis, Photophysical, and Cytotoxic Studies
2019 · Hamid R. Shahsavari, Nora Giménez, et al. · European Journal of Inorganic Chemistry · 33
Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease
2020 · Mohammad Mehdi Heidari, Fatemeh Sadat Mirfakhradini, et al. · Applied Biochemistry and Biotechnology · 30
Upregulation of miR-222 in both Helicobacter pylori-infected and noninfected gastric cancer patients
2016 · MINA NOORMOHAMMAD, SAMIRA SADEGHI, et al. · Journal of Genetics · 25
Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome
2017 · Mahsasadat Fallah Tafti, Mehri Khatami, et al. · Cardiology Journal · 23
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Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients
2019 · Sima Dianatpour, Mehri Khatami, et al. · Applied Biochemistry and Biotechnology · 21
Relationship of the MTHFD1 (rs2236225), eNOS (rs1799983), CBS (rs2850144) and ACE (rs4343) gene polymorphisms in a population of Iranian pediatric patients with congenital heart defects
2017 · Mehri Khatami, Farzaneh Morteza Ratki, et al. · The Kaohsiung Journal of Medical Sciences · 20
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Mitochondrial Genetic Variation in Iranian Infertile Men with Varicocele.
2016 · Mohammad Mehdi Heidari, Mehri Khatami, et al. · PubMed Central · 20
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CDR grafting and site-directed mutagenesis approach for the generation and affinity maturation of Anti-CD20 nanobody
2024 · Mohammad Mehdi Heidari, Elham Anbar Shirazi, et al. · Molecular Biology Reports · 18
A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia
2008 · Mohammad Mehdi Heidari, Massoud Houshmand, et al. · Cellular and Molecular Neurobiology · 17
Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease
2022 · Mohammad Mehdi Heidari, Mehri Khatami, et al. · EXCLI journal · 16
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Protective effect of Berberis vulgaris on Fenton reaction-induced DNA cleavage.
2019 · Nooshin Sadat Asadi, Mohammad Mehdi Heidari, et al. · PubMed Central · 16
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Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease
2018 · Mehri Khatami, Mansoureh Mazidi, et al. · Medicina · 16
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Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis
2017 · Mohammad Mehdi Heidari, Mehri Khatami, et al. · Basic and Clinical Neuroscience Journal · 15
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Polymorphisms in NOS3, MTHFR, APOB and TNF-α genes and risk of coronary atherosclerotic lesions in Iranian patients
2015 · MohammadMehdi Heidari, Mehri Khatami, et al. · Research in Cardiovascular Medicine · 15
Mutation analysis of TNP1 gene in infertile men with varicocele.
2014 · Mohammad Mehdi Heidari, Mehri Khatami, et al. · Europe PMC (PubMed Central) · 15
The POLG Gene Polymorphism in Iranian Varicocele-Associated Infertility Patients.
2012 · Mohammad Mehdi Heidari, Mehri Khatami, et al. · PubMed Central · 15
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The association of renin–angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss
2017 · Mohammad Mehdi Heidari, Mozhgan Sheikholeslami, et al. · Human Fertility · 14
Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects
2018 · Mehri Khatami, Mohammad Mehdi Heidari, et al. · Journal of Cardiovascular and Thoracic Research · 13
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Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?
2009 · Mehri Khatami, Massoud Houshmand, et al. · Cardiovascular Pathology · 12
Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)
2021 · Faranak Ghadamyari, Mohammad Mehdi Heidari, et al. · Journal of Clinical Laboratory Analysis · 11
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Relationship of hypomethylation CpG islands in interleukin-6 gene promoter withIL-6mRNA levels in patients with coronary atherosclerosis
2020 · Monireh Mohammadpanah, Mohammad Mehdi Heidari, et al. · Journal of Cardiovascular and Thoracic Research · 11
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Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism
2017 · Mehri Khatami, Mohammad Mehdi Heidari, et al. · Journal of Pediatric Endocrinology and Metabolism · 11
Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR.
2017 · Mehri Khatami, Mohammad Mehdi Heidari, et al. · PubMed Central · 10
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Works count: 87
Citation count: 641
H-index: 15
I10-index: 25
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