Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the In-Silico and In-Vitro Evidence Suggest Linc01405 As a Sponge for Mir-29B and Mir-497-5P, and a Potential Regulator of Wnt, Pi3k, and Tgfb Signaling Pathways in Breast Carcinoma
Mohsen Ghadami

Associate Professor of Medical Genetics

Department Medical Genetics

School of Medicine

Shariati Hospital

Tehran University of Medical Sciences

All Documents
1. Disruption of Linc00265/Mir-101-3P Axis Using Sirna Suppresses Growth and Promotes Apoptosis in Laryngeal Cancer Cells, Gene Reports (2026)
2. Identification of a Putative Founder Effect Involving the Hace1:C.1396C>T Variant in Two Iranian Families and Review of Reported Cases, Neurological Sciences (2026)
3. Circular Rnas in Glioblastoma, Clinica Chimica Acta (2025)
4. Circznf609 and Circnfix As Possible Regulators of Glioblastoma Pathogenesis Via Mir-145-5P/Egfr Axis, Scientific Reports (2024)
5. Microrna Biosensors for Detection of Glioblastoma, Clinica Chimica Acta (2024)
6. Relationship Between Fsh Receptor’S Exon 10 Polymorphisms With Ivf Results in Iranian Women, Journal of Payavard Salamat (2024)
7. Comparison of Plasma Levels of Microrna-155-5P, Microrna-210-3P, and Microrna-16-5P in Rheumatoid Arthritis Patients With Healthy Controls in a Case-Control Study, Iranian Journal of Allergy# Asthma and Immunology (2023)
8. Clinical and Molecular Assessment of Iranian Families With Severe Congenital Neutropenia, Identification of Hyou1 and Shoc2 As Potential Novel Gene Defects, Iranian Journal of Allergy# Asthma and Immunology (2022)
9. Clinical and Molecular Assessment of Iranian Families With Severe Congenital Neutropenia, Identification of Hyou1 and Shoc2 As Potential Novel Gene Defects, Iranian Journal of Allergy, Asthma and Immunology (2022)
10. Novel Exosc9 Variants Cause Pontocerebellar Hypoplasia Type 1D With Spinal Motor Neuronopathy and Cerebellar Atrophy, Journal of Human Genetics (2021)
11. Novel Exosc9 Variants Cause Pontocerebellar Hypoplasia Type 1D With Spinal Motor Neuronopathy and Cerebellar Atrophy, Journal of Human Genetics (2021)
12. Plasma Levels of Microrna-146A-5P, Microrna-24-3P, and Microrna-125A-5P As Potential Diagnostic Biomarkers for Rheumatoid Arthritis, Iranian Journal of Allergy# Asthma and Immunology (2021)
13. Ret Proto-Oncogene Mutational Analysis in 45 Iranian Patients Affected With Medullary Thyroid Carcinoma: Report of a New Variant, Journal of Thyroid Research (2021)
14. Determination of Association Between the Polymorphism in Exon 3 of Dopamine Receptor Gene Type 4 With Attention Deficit-Hyperactivity Disorder, Clinical Epidemiology and Global Health (2020)
15. Investigation of Promoter Methylation of Fscn1 Gene and Fscn1 Protein Expression in Differentiated Thyroid Carcinomas, Molecular Biology Reports (2020)
16. Rpe65 and Retinal Dystrophy: Report of New and Recurrent Mutations, Journal of Gene Medicine (2020)
17. Variable Clinical Manifestations of Covid-19: Viral and Human Genomes Talk, Iranian Journal of Allergy# Asthma and Immunology (2020)
18. Cell Free Tumoral Dna Versus Paraffin Block Epidermal Growth Factor Receptor Mutation Detection in Patients With Non-Small Cell Lung Cancer, Asian Pacific Journal of Cancer Prevention (2019)
19. Evaluation of the Prevalence of Exons 1 and 10 Polymorphisms of Lhcgr Gene and Its Relationship With Ivf Success, Journal of Reproduction and Infertility (2019)
20. The First Cohort of Iranian Patients With Hyper Immunoglobulin E Syndrome: A Long-Term Follow-Up and Genetic Analysis, Pediatric Allergy and Immunology (2019)
21. The First Cohort of Iranian Patients With Hyper Immunoglobulin E Syndrome: A Long-Term Follow-Up and Genetic Analysis, Pediatric Allergy and Immunology (2019)
22. Association of Sp-B Gene 9306 A/G Polymorphism (Rs7316) and Risk of Rds, Journal of Maternal-Fetal and Neonatal Medicine (2018)
23. Clinical, Immunologic, and Genetic Spectrum of 696 Patients With Combined Immunodeficiency, Journal of Allergy and Clinical Immunology (2018)
24. Clinical, Immunologic, and Genetic Spectrum of 696 Patients With Combined Immunodeficiency, Journal of Allergy and Clinical Immunology (2018)
25. Evaluation of the Potential Association Between Cannabinoid Receptor 2 Gene Q63r Polymorphism (Rs35761398) and Risk of Rds Development in Preterm Neonates, Iranian Journal of Pediatrics (2018)
26. Association of Sp-C Gene Codon 186 Polymorphism (Rs1124) and Risk of Rds, Journal of Maternal-Fetal and Neonatal Medicine (2017)
27. Demethylation and Alterations in the Expression Level of the Cell Cycle–Related Genes As Possible Mechanisms in Arsenic Trioxide–Induced Cell Cycle Arrest in Human Breast Cancer Cells, Tumor Biology (2017)
28. Investigation of Itgb2 Gene in 12 New Cases of Leukocyte Adhesion Deficiency-Type I Revealed Four Novel Mutations From Iran, Archives of Iranian Medicine (2015)
29. Investigation of Itgb2 Gene in 12 New Cases of Leukocyte Adhesion Deficiency-Type I Revealed Four Novel Mutations From Iran, Archives of Iranian Medicine (2015)
30. Mutations in the Histamine N-Methyltransferase Gene, Hnmt, Are Associated With Nonsyndromic Autosomal Recessive Intellectual Disability, Human Molecular Genetics (2015)