| # | Title | Journal | Year | Citations |
|---|
| 1 | A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family | American Journal of Human Genetics | 2008 | 84 |
| 2 | OCT4B1, a novel spliced variant of OCT4, is highly expressed in gastric cancer and acts as an antiapoptotic factor | International Journal of Cancer | 2011 | 68 |
| 3 | Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11 | Clinical Genetics | 2008 | 58 |
| 4 | Association of p53/p21 expression with cigarette smoking and prognosis in esophageal squamous cell carcinoma patients | World Journal of Gastroenterology | 2010 | 42 |
| 5 | Do Haplogroups H and U Act to Increase the Penetrance of Alzheimer’s Disease? | Cellular and Molecular Neurobiology | 2007 | 39 |
| 6 | Gene Expression Profiling of Mitochondrial Oxidative Phosphorylation (OXPHOS) Complex I in Friedreich Ataxia (FRDA) Patients | PLoS ONE | 2014 | 32 |
| 7 | Liver Mitochondrial DNA Copy Number and Deletion Levels May Contribute to Nonalcoholic Fatty Liver Disease Susceptibility | Hepatitis Monthly | 2016 | 28 |
| 8 | Global landscape of SARS-CoV-2 mutations and conserved regions | Journal of Translational Medicine | 2023 | 26 |
| 9 | ΔmtDNA4977 Is More Common in Non-tumoral Cells from Gastric Cancer Sample | Archives of Medical Research | 2006 | 24 |
| 10 | Koenimbin, a natural dietary compound of Murraya koenigii (L) Spreng: inhibition of MCF7 breast cancer cells and targeting of derived MCF7 breast cancer stem cells (CD44+/CD24-/low): an in vitro study | Drug Design, Development and Therapy | 2015 | 22 |
| 11 | Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients | Multiple Sclerosis Journal | 2005 | 20 |
| 12 | Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment | Clinical Interventions in Aging | 2016 | 20 |
| 13 | Role of orexin-A in experimental autoimmune encephalomyelitis | Journal of Neuroimmunology | 2016 | 20 |
| 14 | Age-related decrease in mtDNA content as a consequence of mtDNA 4977 bp deletion | Mitochondrial DNA Part A: DNA Mapping, Sequencing, and Analysis | 2016 | 16 |
| 15 | Tumoral Cell mtDNA ∼8.9 kb Deletion Is More Common than Other Deletions in Gastric Cancer | Archives of Medical Research | 2006 | 14 |
| 16 | Usage of mitochondrial D-loop variation to predict risk for Huntington disease | Mitochondrial DNA | 2015 | 14 |
| 17 | The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis | Therapeutics and Clinical Risk Management | 2016 | 14 |
| 18 | Proteome analysis of post-transplantation recovery mechanisms of an EAE model of multiple sclerosis treated with embryonic stem cell-derived neural precursors | Journal of Proteomics | 2013 | 12 |
| 19 | Mitochondrial Mutation in Iranian Patients with Multiple Sclerosis, Correlation Between Haplogroups H, A and Clinical Manifestations | Cellular and Molecular Neurobiology | 2009 | 10 |
| 20 | Association of interleukin-1 gene polymorphism with risk of gastric and colorectal cancers in an Iranian population | Iranian Journal of Immunology | 2018 | 10 |
| 21 | Mitochondrial D-Loop Variation in Leber Hereditary Neuropathy Patients Harboring Primary G11778A, G3460A, T14484C Mutations: J and W Haplogroups as High-Risk Factors | Archives of Medical Research | 2006 | 9 |
| 22 | Assessment of Bone Morphogenetic Protein 3 Methylation in Iranian Patients with Colorectal Cancer | Middle East Journal of Digestive Diseases | 2017 | 9 |
| 23 | Network analysis and the impact of Aflibercept on specific mediators of angiogenesis in HUVEC cells | Journal of Cellular and Molecular Medicine | 2021 | 8 |
| 24 | Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from Iran | Iranian Journal of Pediatrics | 2013 | 8 |
| 25 | Identification of a new human mtDNA polymorphism (A14290G) in the NADH dehydrogenase subunit 6 gene | Brazilian Journal of Medical and Biological Research | 2006 | 7 |
| 26 | DOCK8 deficiency in six Iranian patients | Clinical Case Reports (discontinued) | 2016 | 7 |
| 27 | Increase in mRNA Level of Orexin1 and 2 Receptors Following Induction of Experimental Autoimmune Encephalomyelitis in Mice | Iranian Journal of Allergy, Asthma and Immunology | 2016 | 6 |
| 28 | Diversity and relationship between Iranian ethnic groups: Human dopamine transporter gene (DAT1) VNTR genotyping | American Journal of Human Biology | 2007 | 4 |
| 29 | 8q24.3 and 11q25 chromosomal loci association with low HDL-C in metabolic syndrome | European Journal of Clinical Investigation | 2011 | 4 |
| 30 | Four novel mutations of the BCKDHA, BCKDHB and DBT genes in Iranian patients with maple syrup urine disease | Journal of Pediatric Endocrinology and Metabolism | 2018 | 4 |
| 31 | False Negative Mitigation in Group Testing for COVID-19 Screening | Frontiers in Medicine | 2021 | 4 |
| 32 | Association of human mtDNA mutations with autism in Iranian patients | Journal of Research in Medical Sciences | 2013 | 4 |
| 33 | The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family | Iranian Journal of Basic Medical Sciences | 2014 | 4 |
| 34 | The Study of rs693 and rs515135 in APOB in People with Familial Hypercholestrolemia | Cell Journal | 2019 | 4 |
| 35 | Allele Frequency Distribution Data for D8S1132, D8S1779, D8S514, and D8S1743 in Four Ethnic Groups in Relation to Metabolic Syndrome: Tehran Lipid and Glucose Study | Biochemical Genetics | 2009 | 3 |
| 36 | Molecular and clinical investigation of Iranian patients with Friedreich ataxia | Iranian Biomedical Journal | 2014 | 3 |
| 37 | The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia | Journal of Medicine and Life | 2022 | 2 |
| 38 | Allele frequency distribution for D11S1304, D11S1998, and D11S934 and metabolic syndrome in TLGS | European Journal of Lipid Science and Technology | 2010 | 1 |
| 39 | The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men | Genes and Genomics | 2023 | 1 |
| 40 | Allele Frequency of D12S1632, D12S329, D12S96, D16S3096 and D16S2624 in four Ethnic Groups and Its Relationship With Metabolic Syndrome in Tehran Lipid and Glucose Study | Gene, Cell and Tissue | 2014 | 0 |
| 41 | Analysis of Mitochondrial 4977-bp Deletion and D-Loop Variation in Iranian Non-Alcoholic Fatty Liver Disease Patients | Hepatitis Monthly | 2019 | 0 |
| 42 | Evaluation of microRNA Gene Polymorphisms in Liver Transplant Patients with Hepatocellular Carcinoma | Hepatitis Monthly | 2020 | 0 |
| 43 | Involvement of single nucleotide polymorphisms in acute lymphoblastic leukemia susceptibility | Gene Reports | 2020 | 0 |
| 44 | A Splicing Variant in OCRL Gene Might Explain the Second Case of Lowe Syndrome in Iran | Journal of Human Genetics and Genomics | 2020 | 0 |
| 45 | Glutaric AciduriaType 1: Clinical and Molecular Study in Iranian Patients, 3 Novel Mutations | Iranian Journal of Child Neurology | 2017 | 0 |
