Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the Cel Gene
Mahsa Mohamad Amoli
Mahsa Mohamad Amoli

Professor of Genetics

Metabolic Disorders Research Center

Endocrinology and Metabolism Research Institute

Tehran University of Medical Sciences

All Documents
1. Genetic Variant Profiling of Neonatal Diabetes Mellitus in Iranian Patients: Unveiling 58 Distinct Variants in 14 Genes, Journal of Diabetes Investigation (2024)
2. Protocol for Preliminary, Multicenteric Validation of Pocosteo Device: A Point of Care Tool for Proteomic and Genomic Study of Osteoporosis, Biology Methods and Protocols (2024)
3. Ace I/D Gene Polymorphisms and Polycystic Ovary Syndrome Manifestations, Journal of Diabetes and Metabolic Disorders (2023)
4. Association of Ace Gene Polymorphisms With In-Stent Restenosis by Stent Type (Biomime, Supraflex, Xience), Molecular Biology Reports (2023)
5. Association of the Apoe Gene Variants With Depression in Type 2 Diabetes, Journal of Diabetes and Metabolic Disorders (2023)
6. Haplotypic Variants of Covid-19 Related Genes Are Associated With Blood Pressure and Metabolites Levels, Journal of Medical Virology (2023)
7. Investigating the Relationship Between the Vntr Variant of the Interleukin-1 Receptor Antagonist Gene and Coronary In-Stent Restenosis, Molecular Biology Reports (2023)
8. Metformin and Long Non-Coding Rnas in Breast Cancer, Journal of Translational Medicine (2023)
9. Pten Promoter Methylation and Expression in Endometrial Cancer Tissues, Epigenomics (2023)
10. Adenosine Deaminase Gene Variant in Diabetes and Obesity, Journal of Diabetes and Metabolic Disorders (2022)
11. An Application of Cart Algorithms for Detection of an Association Between Vdr Polymor-Phisms and Reduced Bone Density in Individuals With Type 2 Diabetes: A Population-Based Cross-Sectional Study, Journal of Biostatistics and Epidemiology (2022)
12. Association of Mirna Targetome Variants in Lamc1 and Gnb3 Genes With Colorectal Cancer and Obesity, Cancer Medicine (2022)
13. Early and Delayed Puberty Among Iranian Children With Obesity, Minerva Endocrinology (2022)
14. Investigating Genetic Mutations in a Large Cohort of Iranian Patients With Congenital Hyperinsulinism, JCRPE Journal of Clinical Research in Pediatric Endocrinology (2022)
15. Investigation of Genetic Factors Associated With Polycystic Ovary Syndrome, Koomesh (2022)
16. Local Insulin-Derived Amyloidosis Model Confronted With Silymarin: Histological Insights and Gene Expression of Mmp, Tnf-Α, and Il-6, International Journal of Molecular Sciences (2022)
17. Multivariate and Gene-Based Association Testing of Sarcopenia: Bushehr Elderly Health Program (Beh), Journal of Biostatistics and Epidemiology (2022)
18. Precision Medicine Initiatives, Precision Medicine in Clinical Practice (2022)
19. Relationship Between a Near Melanocortin-4 Receptor Gene Variant and Puberty Timing in Children Is Vague Unlike Obesity, Journal of Diabetes and Metabolic Disorders (2022)
20. Role of Genetic Polymorphisms in Recurrent Aphthous Stomatitis: A Systematic Review and Meta-Analysis, Cytokine (2022)
21. Study of the Frequency and Clinical Features of Maturity-Onset Diabetes in the Young in the Pediatric and Adolescent Diabetes Population in Iran, Journal of Pediatric Endocrinology and Metabolism (2022)
22. The Importance of Regulatory Pathway Mediated by Circ0001955 in Colorectal Cancer, Experimental and Molecular Pathology (2022)
23. The Role of Inflammatory Mirna–Mrna Interactions in Pbmcs of Colorectal Cancer and Obesity Patients, Immunity# Inflammation and Disease (2022)
24. The Vitamin D Receptor Gene Variants, Apai, Taqi, Bsmi, and Foki in Diabetic Foot Ulcer and Their Association With Oxidative Stress, Molecular Biology Reports (2022)
25. Vascular Endothelial Growth Factor Genetic Variant Is Associated With In-Stent Restenosis After Percutaneous Coronary Intervention, Journal of Tehran University Heart Center (2022)
26. Ada Gene Haplotype Is Associated With Coronary-In-Stent-Restenosis, Molecular Biology Reports (2021)
27. Association of Pro-Inflammatory Cytokine Gene Polymorphism With Meniere’S Disease in an Iranian Sample, Iranian Journal of Allergy# Asthma and Immunology (2021)
28. Association of Vitamin D Receptor Gene Polymorphism With the Occurrence of Low Bone Density, Osteopenia, and Osteoporosis in Patients With Type 2 Diabetes, Journal of Diabetes and Metabolic Disorders (2021)
29. Comments on Effects of Mtnr1b Genetic Variants on Individual Susceptibility to Gestational Diabetes Mellitus: A Meta-Analysis, American Journal of Perinatology (2021)
30. Differentially Expressed Mir-152, a Potential Biomarker for In-Stent Restenosis (Isr) in Peripheral Blood Mononuclear Cells (Pbmcs) of Coronary Artery Disease (Cad) Patients, Nutrition# Metabolism and Cardiovascular Diseases (2021)
31. Evaluation of Errfi1 +808 T/G Variant and Its Mrna Expression in Coronary Artery In-Stent Restenosis, Gene Reports (2021)
32. Genetic Research in Immunogenetics Group of Endocrinology and Metabolism Research Institute, Journal of Diabetes and Metabolic Disorders (2021)
33. Hydro Alcoholic Green Tea Extract Effect on High Fat Diet Treated Nmri Mice and 3T3l1 Cells, Journal of Diabetes and Metabolic Disorders (2021)
34. Investigating the Association of Matrix Metalloproteinase-2 Gene Variants With Endometriosis in an Iranian Population, European Journal of Obstetrics and Gynecology and Reproductive Biology (2021)
35. Investigation of Tgf-Β1 Gene Variant and Expression in a Group of Iranian Women With Endometriosis, Archives of Gynecology and Obstetrics (2021)
36. Knowledge Discovery in Genetics of Diabetes in Iran, a Roadmap for Future Researches, Journal of Diabetes and Metabolic Disorders (2021)
37. Meglitinide (Repaglinide) Therapy in Permanent Neonatal Diabetes Mellitus: Two Case Reports, Journal of Medical Case Reports (2021)
38. The Effect of Metformin on Expression of Long Non-Coding Rna H19 in Endometrial Cancer, Medical Journal of the Islamic Republic of Iran (2021)
39. Thyroid Cancer Research at Endocrinology and Metabolism Research Institute (Emri): A Report of Scientific Activities Between 2005 and 2020, Journal of Diabetes and Metabolic Disorders (2021)
40. Vegfa Gene Haplotypes in Meniere's Disease, Gene Reports (2021)
41. An in Silico Approach to Identify and Prioritize Mirnas Target Sites Polymorphisms in Colorectal Cancer and Obesity, Cancer Medicine (2020)
42. Association of Microrna Gene Polymorphisms With Type 2 Diabetes Mellitus: A Systematic Review and Meta-Analysis, Journal of Research in Medical Sciences (2020)
43. Association of Mthfr C677t Polymorphism With Elevated Homocysteine Level and Disease Development in Vitiligo, International Journal of Immunogenetics (2020)
44. Comments on and Assessment of “The Rs498872 Polymorphism Is Associated With an Elevated Susceptibility to Glioma: A Meta-Analysis of 36,264 Subjects”, Acta Neurologica Belgica (2020)
45. Comments on and Assessments of ‘Associations Between Endothelial Nitric Oxide Synthase Gene Polymorphisms and the Risk of Coronary Artery Disease: A Systematic Review and Meta-Analysis of 132 Case–Control Studies’, European Journal of Preventive Cardiology (2020)
46. Comments on and Assessments of ‘Associations Between Fcgr Polymorphisms and Immune Thrombocytopenia: A Meta-Analysis’, Scandinavian Journal of Immunology (2020)
47. Letter to the Editor: Association Between Α-Adducin Rs4961 Polymorphism and Hypertension: A Meta-Analysis Based on 40 432 Subjects, Journal of Cellular Biochemistry (2020)
48. Sex-Dependent Association of Ace (I/D) Polymorphism With Meniere's Disease, Meta Gene (2020)
49. A Case of H Syndrome With a Novel Mutation in Slc29a3, Meta Gene (2019)
50. Association of Interleukin-6 Polymorphisms With Obesity: A Systematic Review and Meta-Analysis, Cytokine (2019)
51. Association of Vascular Endothelial Growth Factor (Vegf) Gene Polymorphisms and Expression With the Risk of Endometriosis: A Case–Control Study, Molecular Biology Reports (2019)
52. Autoimmune Polyglandular Syndrome Type 1: A Case Report, BMC Medical Genetics (2019)
53. Cdh1 and Ddr1 Common Variants Confer Risk to Vitiligo and Autoimmune Comorbidities, Gene (2019)
54. Comments on “Association Between Mir-499 Rs3746444 Polymorphism and Coronary Heart Disease Susceptibility: An Evidence-Based Meta-Analysis of 5063 Cases and 4603 Controls”, Gene (2019)
55. Comments on “Correlation Between Pnpla3 Rs738409 Polymorphism and Hepatocellular Carcinoma: A Meta-Analysis of 10,330 Subjects”, International Journal of Biological Markers (2019)
56. Comments On: “A Meta-Analysis of the Association Between Microrna-196A2 and Risk of Ischemic Stroke and Coronary Artery Disease in Asian Population”, Journal of Stroke and Cerebrovascular Diseases (2019)
57. Comments On: “Meta-Analysis of Association Between Arg326gln (Rs1503185) and Gln276pro (Rs1566734) Polymorphisms of Ptprj Gene and Cancer Risk”, Journal of Applied Genetics (2019)
58. Competing Endogenous Rna (Cerna) Cross Talk and Language in Cerna Regulatory Networks: A New Look at Hallmarks of Breast Cancer, Journal of Cellular Physiology (2019)
59. Haplotypes in Vitamin D Receptor Gene Encode Risk in Diabetic Nephropathy, Gene (2019)
60. Inflammation Related Mirnas As an Important Player Between Obesity and Cancers, Journal of Diabetes and Metabolic Disorders (2019)
61. Influence of Antioxidants' Gene Variants on Risk of Diabetes Mellitus and Its Complications: A Systematic Review, Minerva Endocrinologica (2019)
62. Integrative Analyses of Triple Negative Dysregulated Transcripts Compared With Non-Triple Negative Tumors and Their Functional and Molecular Interactions, Journal of Cellular Physiology (2019)
63. Investigating the Association of Rs2346061 (Cndp1), Rs7577 (Cndp2), and Rs1801133 (Mthfr) Variants and Homocysteine Level With Diabetic Nephropathy in an Iranian Population, Gene Reports (2019)
64. Iranian Neonatal Diabetes Mellitus Due to Mutation in Pdx1 Gene: A Case Report, Journal of Medical Case Reports (2019)
65. Is the +405 G/C Single Nucleotide Polymorphism of the Vascular Endothelial Growth Factor (Vegf) Gene Associated With Late-Onset Vitiligo?, International Journal of Immunogenetics (2019)
66. Letter to the Editor: Comments on “Association Between the Icam-1 Gene Polymorphism and Coronary Heart Disease Risk: A Meta-Analysis”, Bioscience Reports (2019)
67. Macrophage Migration Inhibitory Factor Polymorphism (Rs755622) in Alopecia Areata: A Possible Role in Disease Prevention, Archives of Dermatological Research (2019)
68. Microrna-Binding Site Polymorphisms and Risk of Colorectal Cancer: A Systematic Review and Meta-Analysis, Cancer Medicine (2019)
69. Mif 173 G>C Variation Was Associated With Depressive Disorder in Type 2 Diabetes in an Iranian Population, Psychoneuroendocrinology (2019)
70. Mthfr and Apoe Genetic Variants Association With Sudden Sensorineural Hearing Loss, American Journal of Otolaryngology - Head and Neck Medicine and Surgery (2019)
71. Over-Expression of Tgf-Β1 Gene in Medication Free Schizophrenia, Psychoneuroendocrinology (2019)
72. Overall Corrections and Assessments of “Correlations Between Tlr Polymorphisms and Inflammatory Bowel Disease: A Meta-Analysis of 49 Case-Control Studies”, Immunologic Research (2019)
73. Re: Association Between the Cyp4f2 Gene Rs1558139 and Rs2108622 Polymorphisms and Hypertension: A Meta-Analysis by Geng Et Al. (Genet Test Mol Biomarkers 2019;23:342-347; Doi: 10.1089/Gtmb.2018.0202), Genetic Testing and Molecular Biomarkers (2019)
74. Role of Vitamin D and Vitamin D Receptor Gene Polymorphisms on Residual Beta Cell Function in Children With Type 1 Diabetes Mellitus, Pharmacological Reports (2019)
75. The Association Analysis of Vascular Endothelial Growth Factor-2549 Insertion/ Deletion Variant and Endometriosis Risk, International Journal of Molecular and Cellular Medicine (2019)
76. The Association Between Genetic Variation in Wnt Transcription Factor Tcf7l2 (Tcf4) and Alopecia Areata, Immunological Investigations (2019)
77. The Role of Errfi1+808T/G Polymorphism in Diabetic Nephropathy, International Journal of Molecular and Cellular Medicine (2019)
78. Type 1 Diabetes Genetic Risk Score Discriminates Between Monogenic and Type 1 Diabetes in Children Diagnosed at the Age of <5 Years in the Iranian Population, Diabetic Medicine (2019)
79. A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes, Canadian Journal of Diabetes (2018)
80. Association Between Epstein Barr Virus and Tongue Squamous Cell Carcinoma in Iranian Patients, Pathology Research and Practice (2018)
81. Association Between Mthfr Variant and Diabetic Neuropathy, Pharmacological Reports (2018)
82. Association Between the Polymorphism of Glu298asp in Exon 7 of the Enos Gene With Foot Ulcer and Oxidative Stress in Adult Patients With Type 2 Diabetes, Canadian Journal of Diabetes (2018)
83. Association Between Trp48arg Polymorphism of the Cd11c Gene and Risk for Obesity Among Iranian Population, Journal of Diabetes and Metabolic Disorders (2018)
84. Enos Gene Glu298asp Variant Confer Risk in Sudden Sensorineural Hearing Loss, Acta Oto-Laryngologica (2018)
85. Potential Role of Gender Specific Effect of Leptin Receptor Deficiency in an Extended Consanguineous Family With Severe Early-Onset Obesity, European Journal of Medical Genetics (2018)
86. Slc34a3 Intronic Deletion in an Iranian Kindred With Hereditary Hypophosphatemic Rickets With Hypercalciuria, JCRPE Journal of Clinical Research in Pediatric Endocrinology (2018)
87. The P.Arg435his Variation of Igg3 With High Affinity to Fcrn Is Associated With Susceptibility for Pemphigus Vulgaris-Analysis of Four Different Ethnic Cohorts, Frontiers in Immunology (2018)
88. Adiponectin Gene Variants and Abdominal Obesity in an Iranian Population, Eating and Weight Disorders (2017)
89. Association Between 318C/T Polymorphism of the Ctla-4 Gene and Systemic Lupus Erythematosus in Iranian Patients, International Journal of Rheumatic Diseases (2017)
90. Comparison of Moderate and High Volume Aerobic Training on Gene Expression of Uncoupling Protein 1 (Ucp-1) in Subcutaneous White Adipose Tissue of Wistar Rats, Iranian Journal of Endocrinology and Metabolism (2017)
91. Congenital Generalized Lipodystrophy in a Youth Presented With Sclerotic and Lytic Bone Lesions; a Family With Agpat2 Mutation, International Journal of Pediatrics (2017)
92. Evaluation of the Presence of Epstein-Barr Virus (Ebv) in Iranian Patients With Thyroid Papillary Carcinoma, Pathology Research and Practice (2017)
93. Liver Alpha-Amylase Gene Expression As an Early Obesity Biomarker, Pharmacological Reports (2017)
94. Methylomics of Breast Cancer: Seeking Epimarkers in Peripheral Blood of Young Subjects, Tumor Biology (2017)
95. Non-Muscle Myosin Heavy Chain 9 Gene (Myh9) Polymorphism (Rs4821481) Is Associated With Urinary Albumin Excretion in Iranian Diabetic Patients, Iranian Red Crescent Medical Journal (2017)
96. Polymorphisms of Antioxidant Genes As a Target for Diabetes Management, International Journal of Molecular and Cellular Medicine (2017)
97. Vitamin D Receptor Gene Foki Variant in Diabetic Foot Ulcer and Its Relation With Oxidative Stress, Gene (2017)
98. Benzothiazole Thioflavin T Improves Obesity-Related Symptoms in Mice, Periodicum Biologorum (2016)
99. Effect of Inulin Supplementation in Male Mice Fed With High Fat Diet on Biochemical Profile and Α-Amylase Gene Expression, Tropical Journal of Pharmaceutical Research (2016)
100. Hla-Cw Allele Frequency in Definite Meniere's Disease Compared to Probable Meniere's Disease and Healthy Controls in an Iranian Sample, Iranian Journal of Otorhinolaryngology (2016)
101. Molecular Investigation of Wfs1 Gene Exon 8 in Iranian Patients With Wolfram Syndrome, International Journal of Diabetes in Developing Countries (2016)
102. Acarbose Versus Transchalcone: Comparing the Effect of Two Glycosidase Inhibitors on Obese Mice, Archives of Endocrinology and Metabolism (2015)
103. Association Between Ctla-4 Gene Polymorphism and the Risk of Systemic Lupus Erythematosus: Brief Report, Tehran University Medical Journal (2015)
104. Association Between Genetic Variants and Diabetes Mellitus in Iranian Populations: A Systematic Review of Observational Studies, Journal of Diabetes Research (2015)
105. Association Between Macrophage Migration Inhibitory Factor Gene Variation and Response to Glucocorticoid Treatment in Sudden Sensorineural Hearing Loss, Audiology and Neurotology (2015)
106. Epistatic Interaction Between Adiponectin and Survivin Gene Polymorphisms in Endometrial Carcinoma, Pathology Research and Practice (2015)
107. Interleukin-1 Beta, Interferon-Gamma, and Tumor Necrosis Factor-Alpha Gene Expression in Peripheral Blood Mononuclear Cells of Patients With Coronary Artery Disease, ARYA Atherosclerosis (2015)
108. Prevalence of Osteoporosis and Vitamin D Receptor Gene Polymorphisms (Foki) in an Iranian General Population Based Study (Kurdistan) (Imos), Medical Journal of the Islamic Republic of Iran (2015)
109. Role of the -786T>C Variant of the Endothelial Nitric Oxide Synthase Gene in Stent Restenosis Following Coronary Stent Deployment, Iranian Heart Journal (2015)
110. Sex-Specific Association of Rantes Gene −403 Variant in Meniere’S Disease, European Archives of Oto-Rhino-Laryngology (2015)