Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Novel Tecpr2 Variant in Two Cases of Hereditary Sensory and Autonomic Neuropathy Type 9: Insights From Genetic Characterization and Comprehensive Literature Review
Mina Haji Faraj Tabrizi
Mina Haji Faraj Tabrizi

Assistant Professor of Genetics

Department Medical Genetics

School of Medicine

Tehran University of Medical Sciences

All Documents
1. An Optimized Crispr/Cas12a Assay to Facilitate the Braf V600e Mutation Detection, Journal of Clinical Laboratory Analysis (2024)
2. Distinct Tumor-Tam Interactions in Idh-Stratified Glioma Microenvironments Unveiled by Single-Cell and Spatial Transcriptomics, Acta Neuropathologica Communications (2024)
3. A Patient With Plack Syndrome With a Novel Splicing Mutation in Cast: The Evidence for a Loss-Of-Function Mechanism Through Mis-Splicing, Clinical and Experimental Dermatology (2023)
4. Crispr-Based Fluorescent Reporter (Cbfr) Assay for Sensitive, Specific, Inexpensive, and Visual Detection of a Specific Egfr Exon 19 Deletion in Nsclc, Molecular Biotechnology (2023)
5. Association of Neutrophil to Lymphocyte Ratio and Platelet to Lymphocyte Ratio With Tumoral Differentiation in Colorectal Cancer, Gene Reports (2022)
6. Association of Neutrophil to Lymphocyte Ratio and Platelet to Lymphocyte Ratio With Tumoral Differentiation in Colorectal Cancer, Gene Reports (2022)
7. Data Mining of Bulk and Single-Cell Rna Sequencing Introduces Obi1-As1 As an Astrocyte Marker With Possible Role in Glioma Recurrence and Progression, Clinical Epigenetics (2022)
8. Lipoid Proteinosis Due to Homozygous Deletion Mutation (C.735Deltg) in the Ecm1 Gene Presents With Seizures and Hoarseness But No Skin Involvement, International Journal of Dermatology and Venereology (2022)
9. Molecular and Clinical Characterization of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome (Apeced) in Iranian Non-Jewish Patients: Report of Two Novel Aire Gene Pathogenic Variants, Orphanet Journal of Rare Diseases (2022)
10. Differential Expression of Hypoxia-Related Genes in Primary Brain Tumors and Correlation With Clinicopathologic Data, World Neurosurgery (2021)
11. Catechol-O-Methyltransferase Gene Expression in Stress-Induced and Non-Stress Induced Schizophrenia, Psychiatric Genetics (2020)
12. Decreased Sox2 Messenger Rna Expression in Basal Cell Carcinoma, Indian Journal of Dermatology (2020)
13. Molecular Investigation of Mutations in Androgen Receptor and 5-Alpha-Reductase-2 Genes in 46,Xy Disorders of Sex Development With Normal Testicular Development, Andrologia (2019)
14. Upregulation of Snai2 and Sox9 Mrna Versus Downregulation of Eight Other Emt/Stemness Related Genes in Basal Cell Carcinoma, British Journal of Dermatology (2019)
15. Detection of Ccnd1, C-Myc, and Fgfr1 Amplification Using Modified Sybr Green Qpcr and Fish in Breast Cancer, Turkish Journal of Medical Sciences (2018)
16. Healthy Adult Ldl-C Bears Reverse Association With Serum Il-17A Levels, Current Chemical Genomics and Translational Medicine (2018)
17. Modified Methylated Dna Immunoprecipitation Protocol for Noninvasive Prenatal Diagnosis of Down Syndrome, Journal of Obstetrics and Gynaecology Research (2018)
18. Specific Immune Responses Induced by Multi-Epitope Dna Derived From Mycobacterium Tuberculosis Dosr Antigens, Acta Microbiologica et Immunologica Hungarica (2018)
19. Association of Transcription Factor 4 (Tcf4) Gene Mrna Level With Schizophrenia, Its Psychopathology, Intelligence and Cognitive Impairments, Journal of Neurogenetics (2017)
20. Designing a Novel Multi-Epitope Dna-Based Vaccine Against Tuberculosis: In Silico Approach, Jundishapur Journal of Microbiology (2017)
21. Differential Bmi1, Twist1, Snai2 Mrna Expression Pattern Correlation With Malignancy Type in a Spectrum of Common Cutaneous Malignancies: Basal Cell Carcinoma, Squamous Cell Carcinoma, and Melanoma, Clinical and Translational Oncology (2017)
22. Very Early Onset Inflammatory Bowel Disease: Investigation of the Il-10 Signaling Pathway in Iranian Children, European Journal of Medical Genetics (2017)
23. Very Early Onset Inflammatory Bowel Disease: Investigation of the Il-10 Signaling Pathway in Iranian Children, European Journal of Medical Genetics (2017)
24. Analysis of Knowledge, Attitudes, and Prevalence of Hepatitis B and C Seromarkers Among Barbers in Tehran, Hepatitis Monthly (2016)
25. A Placebo-Controlled Study of Raloxifene Added to Risperidone in Men With Chronic Schizophrenia, Acta Medica Iranica (2015)
26. Comparison of Oral Lichen Planus and Systemic Lupus Erythematosus in Interleukins Level, Archives of Iranian Medicine (2015)
27. Fibroadipose Hyperplasia Versus Proteus Syndrome: Segmental Overgrowth With a Mosaic Mutation in the Pik3ca Gene, Journal of Investigative Dermatology (2015)
28. Lipoid Proteinosis: Phenotypic Heterogeneity in Iranian Families With C.507Delt Mutation in Ecm1, Experimental Dermatology (2015)
29. Detection of Duchenne/Becker Muscular Dystrophy Carriers in a Group of Iranian Families by Linkage Analysis, Acta Medica Iranica (2011)