Mir Davood Omrani

Summary

Country: UK

Publications

  1. doi request reprint The association of TGF-β1 codon 10 polymorphism with suicide behavior
    Mir Davood Omrani
    Faculty of Medicine, Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Am J Med Genet B Neuropsychiatr Genet 159:772-5. 2012
  2. ncbi request reprint Association of interleukin-10, interferon-gamma, transforming growth factor-beta, and tumor necrosis factor-alpha gene polymorphisms with long-term kidney allograft survival
    Mir Davood Omrani
    Deptartment of Genetics, Urmia University of Medical Sciences, Urmia, Iran
    Iran J Kidney Dis 4:141-6. 2010
  3. doi request reprint Role of IL-10 -1082, IFN-gamma +874, and TNF-alpha -308 genes polymorphisms in suicidal behavior
    Mir Davood Omrani
    Department of Genetics, Urmia University of Medical Sciences, Motahari Hospital, Urmia, Iran
    Arch Suicide Res 13:330-9. 2009
  4. doi request reprint A Bioinformatics Approach to the Identification of Variants Associated with Type 1 and Type 2 Diabetes Mellitus that Reside in Functionally Validated miRNAs Binding Sites
    Hamid Ghaedi
    Medical Genetics Department, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Velenjak street, Tehran, Iran
    Biochem Genet 54:211-21. 2016
  5. doi request reprint Association of codon 10 polymorphism of the transforming growth factor beta 1 gene with prostate cancer and hyperplasia in an Iranian population
    Mir Davood Omrani
    Department of Genetics, Urmia Medical Science University, Urmia, Iran
    Urol Int 83:329-32. 2009
  6. doi request reprint The miRNA targetome of coronary artery disease is perturbed by functional polymorphisms identified and prioritized by in-depth bioinformatics analyses exploiting genome-wide association studies
    Milad Bastami
    Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
    Gene 594:74-81. 2016
  7. doi request reprint MiRNA-Related Polymorphisms in miR-146a and TCF21 Are Associated with Increased Susceptibility to Coronary Artery Disease in an Iranian Population
    Milad Bastami
    1 Medical Genetics Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Genet Test Mol Biomarkers 20:241-8. 2016
  8. pmc MAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population
    Shahram Torkamandi
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Int J Mol Cell Med 5:134-140. 2016
  9. pmc A Bioinformatics Approach to Prioritize Single Nucleotide Polymorphisms in TLRs Signaling Pathway Genes
    Behnam Alipoor
    Department of Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
    Int J Mol Cell Med 5:65-79. 2016
  10. doi request reprint A Clone with 5, 17 and 18 Monosomies as Stemline in a Patient with De novo Acute Myeloid Leukemia
    Davood Zare-Abdollahi
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Arch Iran Med 19:379-80. 2016

Collaborators

Detail Information

Publications22

  1. doi request reprint The association of TGF-β1 codon 10 polymorphism with suicide behavior
    Mir Davood Omrani
    Faculty of Medicine, Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Am J Med Genet B Neuropsychiatr Genet 159:772-5. 2012
    ..7%), in comparison with the controls (27%). The findings of this study demonstrated an association between TGF-β1 (codon 10) T/C polymorphisms and suicide behavior...
  2. ncbi request reprint Association of interleukin-10, interferon-gamma, transforming growth factor-beta, and tumor necrosis factor-alpha gene polymorphisms with long-term kidney allograft survival
    Mir Davood Omrani
    Deptartment of Genetics, Urmia University of Medical Sciences, Urmia, Iran
    Iran J Kidney Dis 4:141-6. 2010
    ....
  3. doi request reprint Role of IL-10 -1082, IFN-gamma +874, and TNF-alpha -308 genes polymorphisms in suicidal behavior
    Mir Davood Omrani
    Department of Genetics, Urmia University of Medical Sciences, Motahari Hospital, Urmia, Iran
    Arch Suicide Res 13:330-9. 2009
    ..027). It can be concluded that IL-10, IFN-gamma, and TNF-alpha polymorphisms may play a role in suicidal behavior...
  4. doi request reprint A Bioinformatics Approach to the Identification of Variants Associated with Type 1 and Type 2 Diabetes Mellitus that Reside in Functionally Validated miRNAs Binding Sites
    Hamid Ghaedi
    Medical Genetics Department, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Velenjak street, Tehran, Iran
    Biochem Genet 54:211-21. 2016
    ....
  5. doi request reprint Association of codon 10 polymorphism of the transforming growth factor beta 1 gene with prostate cancer and hyperplasia in an Iranian population
    Mir Davood Omrani
    Department of Genetics, Urmia Medical Science University, Urmia, Iran
    Urol Int 83:329-32. 2009
    ..The role of this polymorphism in the development of prostate cancer and hyperplasia was investigated...
  6. doi request reprint The miRNA targetome of coronary artery disease is perturbed by functional polymorphisms identified and prioritized by in-depth bioinformatics analyses exploiting genome-wide association studies
    Milad Bastami
    Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
    Gene 594:74-81. 2016
    ..The results of this study will be valuable for researchers interested in the identification of CAD GWAS signals that may implicate polymorphic miRNA targeting...
  7. doi request reprint MiRNA-Related Polymorphisms in miR-146a and TCF21 Are Associated with Increased Susceptibility to Coronary Artery Disease in an Iranian Population
    Milad Bastami
    1 Medical Genetics Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Genet Test Mol Biomarkers 20:241-8. 2016
    ....
  8. pmc MAP3K1 May be a Promising Susceptibility Gene for Type 2 Diabetes Mellitus in an Iranian Population
    Shahram Torkamandi
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Int J Mol Cell Med 5:134-140. 2016
    ..44, 95% CI: 1.01-2.05, P = 0.039). In conclusion, we provided the first evidence for the association of rs10461617 at the upstream of MAP3K1 with the risk of T2DM in an Iranian population...
  9. pmc A Bioinformatics Approach to Prioritize Single Nucleotide Polymorphisms in TLRs Signaling Pathway Genes
    Behnam Alipoor
    Department of Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
    Int J Mol Cell Med 5:65-79. 2016
    ..These findings may facilitate the selection of proper variants for future functional and/or association studies. ..
  10. doi request reprint A Clone with 5, 17 and 18 Monosomies as Stemline in a Patient with De novo Acute Myeloid Leukemia
    Davood Zare-Abdollahi
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Arch Iran Med 19:379-80. 2016
    ..It seems that this monosomal karyotype imposed adverse prognosis on this patient and could be related to the rapid and malignant course of the disease as seen. ..
  11. ncbi request reprint CpG island methylation profile of estrogen receptor alpha in Iranian females with triple negative or non-triple negative breast cancer: new marker of poor prognosis
    Fatemeh Ramezani
    Department of Clinical Biochemistry and Nutrition, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran
    Asian Pac J Cancer Prev 13:451-7. 2012
    ..However, methylation of different CpG islands produced a diverse impact on the prognosis of breast cancer, and ER5 was found to be the most frequently methylated region in the Iranian women, and could serve as a marker of poor prognosis...
  12. pmc Allelic frequency and genotypes of prion protein at codon 136 and 171 in Iranian Ghezel sheep breeds
    Siamak Salami
    Department of Biochemistry and Nutrition, Faculty of Medicinem Urmia University of Medical Sciences, Urmia, Iran
    Prion 5:228-31. 2011
    ....
  13. pmc Impact of ATM and SLC22A1 Polymorphisms on Therapeutic Response to Metformin in Iranian Diabetic Patients
    Fazlollah Shokri
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Int J Mol Cell Med 5:1-7. 2016
    ..45, [95% CI 0.64-1.76], P= 0.45) for rs 628031. The reported gene variants in ATM and SLC22A1 are not significantly associated with metformin treatment response in type 2 diabetic patients in an Iranian population. ..
  14. doi request reprint Bioinformatics prioritization of SNPs perturbing microRNA regulation of hematological malignancy-implicated genes
    Hamid Ghaedi
    Medical Genetics Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Genomics 106:360-6. 2015
    ....
  15. ncbi request reprint Are so-called cancer-testis genes expressed only in testis?
    Soudeh Ghafouri-Fard
    Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran E mail
    Asian Pac J Cancer Prev 15:7703-5. 2014
    ..Future research should focus on the expression profiles of so called CT antigens to find those with more testis specific expression. ..
  16. doi request reprint Intact expression status of RASSF1A in acute myeloid leukemia
    Davood Zare-Abdollahi
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Islamic Republic of Iran
    Med Oncol 31:770. 2014
    ..In conclusion, expression status of RASSF1A remained intact in our target samples, indicating that RASSF1A expression variation does not participate in the pathogenesis and the progression of AML...
  17. doi request reprint The Val34Leu genetic variation in the A subunit of coagulation factor XIII in recurrent spontaneous abortion
    Morteza Bagheri
    Faculty of Medicine, Department of Genetics, Urmia University of Medical Sciences, Urmia, Iran
    Syst Biol Reprod Med 57:261-4. 2011
    ..64) corresponding to 95% CI, χ2 = 0.78, p value = 0.37) was not statistically significant. These results suggest that factor XIII Val34Leu genetic variation is not associated with recurrent spontaneous abortion...
  18. pmc PPARγ ameliorated LPS induced inflammation of HEK cell line expressing both human Toll-like receptor 4 (TLR4) and MD2
    Reyhaneh Darehgazani
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Velenjak, 1985717443, Tehran, Iran
    Cytotechnology 68:1337-48. 2016
    ..PPARγ was shown to negatively regulate TLR4 activity and therefore exerts its anti-inflammatory action against LPS induced inflammation. ..
  19. doi request reprint CD29/CD184 expression analysis provides a signature for identification of neuronal like cells differentiated from PBMSCs
    Zahra Fazeli
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Neurosci Lett 630:189-93. 2016
    ..The expression profile of CD29(+/-)/CD184(-) can be suggested as a robust signature for tracing differentiation of Peripheral Blood-Mesenchymal Stem Cells (PB-MSCs) into neuronal cells. ..
  20. doi request reprint Synergistic effects of angiotensinogen -217 G→A and T704C (M235T) variants on the risk of severe preeclampsia
    Farhad Shahvaisizadeh
    Department of Medical Genetics, Medical School, Shahid Beheshti University of Medical Sciences, Iran
    J Renin Angiotensin Aldosterone Syst 15:156-61. 2014
    ..The aims of the present study were to investigate the association between AGT T704C (M235T) and -217 G→A polymorphisms with the risk of preeclampsia and synergistic effects of both polymorphisms on the susceptibility to preeclampsia...
  21. doi request reprint Complex translocation among chromosomes 2, 3, 9, 15, 18, 20 in a patient with 3p-syndrome
    Mir Davood Omrani
    Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
    Arch Iran Med 17:521-2. 2014
    ..3) of the short arm of one of her chromosomes 3. Her karyotype was 46, XX, t(2;18) (p12;q12.1), del(3) (p23p26), t(3;9;15; 20) (q13;p23;q12; p12). Her parents showed a normal karyotype pattern...
  22. pmc Association of catechol-o-methyl transferase gene polymorphism with prostate cancer and benign prostatic hyperplasia
    Mir Davood Omrani
    Department of Genetics, Urmia University of Medical Sciences, Urmia, Iran
    J Res Med Sci 14:217-22. 2009
    ..In this regard, a study was carried out to find a possible association between the COMT gene polymorphism in patients with sporadic prostate cancer (PCa) and benign prostatic hyperplasia (BPH)...