Dr. Iman Abd EL-Mohsen Shaheen
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Dr. Iman Abd EL-Mohsen Shaheen

Professor
Department of Clinical and Chemical Pathology, Chemical Pathology, Faculty of Medicine (Kasr El Aini), Cairo University, Egypt


Highest Degree
Ph.D. in Biomedical Sciences from Cairo University, Egypt

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Area of Interest:

Biomedical Sciences
100%
Molecular Medicine
62%
Leukemia
90%
Platelet Biology
75%
Clinical Pathology
55%

Research Publications in Numbers

Books
0
Chapters
0
Articles
45
Abstracts
0

Selected Publications

  1. Khorshied, M., I. Shaheen, Y. Selim, A. Elshahawy and I. Youssry, 2022. Impact of superoxide dismutase genetic polymorphism (sOD2 vAL16ALA) and superoxide dismutase level on disease severity in a cohort of Egyptian sickle cell disease patients in Egypt. Mediterr. J. Hematol. Infect. Dis., Vol. 14. 10.4084/MJHID.2022.037.
    CrossRef  |  Direct Link  |  
  2. Hamdy, M., I. Shaheen, H.S. El Din, B. Ali and O.A. Dayem, 2022. Klotho level as a marker of low bone mineral density in Egyptian sickle cell disease patients. J. Pediatr. Hematol./Oncol., 44: e40-e45.
    CrossRef  |  Direct Link  |  
  3. Shaheen, I.A., R. Aboukhalil, N. Abulata, R. Abdel-Raouf, B. Meligy and O. Abdel-Dayem, 2021. Vitamin D insufficiency is not associated with pediatric and adolescent immune thrombocytopenia: A study in conjunction with its receptor genetic polymorphisms. J. Pediatr. Hematol./Oncol., 43: e1-e6.
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  4. Hamdy, M., I. Shaheen, Z.M. El-Gammal and Y.M. Ramadan, 2021. Detection of renal insufficiency in a cohort of patients with beta-thalassemia major using cystatin-C. J. Pediatr. Hematol./Oncol., 43: e1082-e1087.
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  5. Shaheen, I., M. Khorshied, R. Abdel-Raouf, H. Gouda and D. Kamal et al., 2020. L-selectin P213S and integrin alpha 2 C807T genetic polymorphisms in pediatric sickle cell disease patients. J. Pediatr. Hematol./Oncol., 42: e707-e711.
    CrossRef  |  Direct Link  |  
  6. Salah, M., I. Shaheen, P. El-Shanawany, N.E. Saad, R. Saad, M. El Guibaly and N. Momen, 2020. Detection of miR-1246, miR-23a and miR-451 in sera of colorectal carcinoma patients: A case-control study in Cairo University hospital. Afr. Health Sci., 20: 1283-1291.
    CrossRef  |  Direct Link  |  
  7. Draz, I.H., I.A. Shaheen and E.A. Youssef, 2020. Platelets count and platelets indices; mean platelet volume and plateletcrit in pediatric chronic lung disease. Egypt. Pediatr. Assoc. Gaz, Vol. 68. 10.1186/s43054-019-0015-5.
    CrossRef  |  Direct Link  |  
  8. Ali, D.K., I.A.M. Shaheen, 2020. The relation between maternal/neonatal vitamin D levels and early onset neonatal sepsis. Am. J. Pediatr., 6: 46-51.
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  9. Abulata, N.N., I.A. Shaheen, O.M. Osman, A.M. Hussein and W.M. El‐Khayat, 2019. The prevalence of combined vascular endothelial growth factor, endothelial nitric oxide synthase and thrombin-activatable fibrinolysis inhibitor genetic polymorphisms among Egyptian patients with recurrent spontaneous abortion. J. Obstet. Gynaecol. Res., 45: 1106-1113.
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  10. El-Masry, M.W., H.M. Gouda, I.A. Shaheen, W. Edesa, N.M. Hassan and R. Ramzy, 2018. Breast cancer resistance protein (BCRP) gene expression in a cohort of adult Egyptian patients with acute myeloid leukemia. Afr. Health Sci., 18: 950-964.
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  11. El Danasori, N., N. Abulata, I.A. Shaheen, A.M. El Gendy and W. El-Khayat, 2018. Thrombin-activatable fibrinolysis inhibitor gene polymorphism (TAFI1040C/T) in women with recurrent spontaneous abortion. Clin. Appl. Thromb. Hemost., 24: 532-535.
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  12. El Mahgoub, I.R., H.M. Gouda, M.A. Samra, I.A.M. Shaheen and A.H.E. Maraashly, 2017. Polymorphisms of xeroderma pigmentosum genes (XPC, XPD, and XPG) and susceptibility to acute leukemia among a sample of Egyptian patients. J. Hematopathol., 10: 3-7.
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  13. Boules, M.L., S.K.A. Botros, I.A. Shaheen and M.A. Hamed, 2015. Association of μ-opioid receptor gene polymorphism (A118G) with variations in fentanyl analgesia consumption after total abdominal hysterectomy in female Egyptian patients. Comp. Clin. Pathol., 24: 241-246.
    CrossRef  |  Direct Link  |  
  14. Aboul-Enein, A., A. EL-Beshlawy, M. Hamdy, I. Shaheen, Z. El-Saadany, A. Samir and H.A. El-Samie, 2015. Peripheral expression of hepcidin gene in Egyptian β-thalassemia major. Gene, 564: 206-209.
    CrossRef  |  Direct Link  |  
  15. Shiba, H.F., M.K. El-Ghamrawy, I.A.E.M. Shaheen, R.A.E.G. Ali and S.M. Mousa, 2014. Glutathione s-transferase gene polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian pediatric patients with sickle cell disease. Pediatr. Dev. Pathol., 17: 265-270.
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  16. Shaheen, I.A., S.K.A. Botros and D.S. Morgan, 2014. Detection of expression of IL-18 and its binding protein in Egyptian pediatric immune thrombocytopenic purpura. Platelets, 25: 193-196.
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  17. Khorshied, M.M., I.A.M. Shaheen, R.E.A. Khalil and R.E. Sheir, 2014. Methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms in chronic myeloid leukemia: An Egyptian study. Med. Oncol., Vol. 31. 10.1007/s12032-013-0794-2.
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  18. Gouda, H.M., M.M. Khorshied, M.H. El Sissy, I.A.M. Shaheen and M.M.A. Mohsen, 2014. Association between matrix metalloproteinase 2 (MMP2) promoter polymorphisms and the susceptibility to non-Hodgkin’s lymphoma in Egyptians. Ann. Hematol., 93: 1313-1318.
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  19. Hamdy, M.S.E.D., H.M. Gouda, I.A.M. Shaheen, M.M. Khorshied and R.H. Tomerak, 2013. Prevalence of factor V leiden (G1619A) and prothrombin gene (G20210A) mutation in Egyptian children with sickle cell disease. Comp. Clin. Pathol., 22: 697-702.
    CrossRef  |  Direct Link  |  
  20. Shaheen, I.A., R.E. Abukhalil, D.K. Ali and R.A. Afifi, 2012. DNMT3B promoter polymorphism and risk of immune thrombocytopenic purpura in pediatric Egyptians. Blood Coagulation Fibrinolysis, 23: 636-639.
    CrossRef  |  PubMed  |  Direct Link  |  
  21. Shaheen, I.A. and N.I. Yehia, 2012. Detection of orphan receptor tyrosine kinase (ROR-1) expression in Egyptian pediatric acute lymphoblastic leukemia. Fetal Pediatr Pathol., 31: 113-119.
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  22. Khorshied, M.M., H.M. Gouda, I.A. Shaheen and T.N. Al-Bolkeny, 2012. The osteogenic differentiation potentials of umbilical cord blood hematopoietic stem cells. Comparat. Clin. Pathol., 21: 441-447.
    CrossRef  |  Direct Link  |  
  23. Farawela, H., M. Khorshied, I. Shaheen, H. Gouda and A. Nasef et al., 2012. The association between hepatitis C virus infection, genetic polymorphisms of oxidative stress genes and B-cell non-Hodgkin's lymphoma risk in Egypt. Infect. Genet. Evol., 12: 1189-1194.
    CrossRef  |  PubMed  |  Direct Link  |  
  24. Eyada, T.K., H.M. Farawela, M.M. Khorshied, I.A. Shaheen, N.M. Selim and I.A. Khalifa, 2012. FcγRIIa and FcγRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt. Blood Coagul Fibrinolysis, 23: 64-68.
    CrossRef  |  PubMed  |  Direct Link  |  
  25. El-Din Hamdy, M.S., H.M. Gouda, I. Abdel-Mohsen Shaheen, M.M. Khorshied and R.H. Tomerak, 2012. Prevalence of factor V Leiden (G1619A) and prothrombin gene (G20210A) mutation in Egyptian children with sickle cell disease. Comparat. Clin. Pathol. J., 10.1007/s00580-012-1469-7.
    CrossRef  |  Direct Link  |  
  26. Arnaout, H.H., M.M. Khorshied, I.A. Shaheen, H.M. Gouda, N.Y. Ibrahim and N.F. Koura, 2012. The clinical significance of methylenetetrahydrofolate reductase (MTHFR) polymorphisms in acute lymphoblastic leukemia. Comparat. Clin. Pathol., 21: 39-47.
    CrossRef  |  Direct Link  |  
  27. Sadek, H., W. El-Metawy, I.A. Shaheen, M. Korshied and A. Mohamad, 2011. Quantitative assessment of Wilms Tumor 1 (WT1) gene transcripts in Egyptian acute lymphoblastic leukemia patients. J. Investig Med., 59: 1258-1262.
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  28. El-Masry, M.W., M.M. Khorshied, I.A. Shaheen, N.N. Abulata and T.A. Hashem, 2011. Flow cytometric detection of leukemic stem cells (LSCs) in Egyptian pediatric B-acute lymphoblastic leukemia. Comparat. Clin. Pathol., 10.1007/s00580-011-1214-7.
    CrossRef  |  Direct Link  |  
  29. El-Karaksy, S.M., N.M. El-Guindy, H.M. Gouda, M.M. Khorshied, I.A. Shaheen, R.E. Abu Khalil and N.Y. Ibrahim, 2011. Clinical relevance of angiopoietin-1, angiopoietin-2, and their receptor Tie-2 expression in acute myeloid leukemia. Comparat. Clin. Pathol., 20: 241-247.
    CrossRef  |  Direct Link  |  
  30. Arnaout, H.H., N. El-Ghrabawy, I.A. Shaheen, R. Afifi and O. Yehia, 2011. Incidence and association of 563 C/T mediterranean and the silent 1311C/T G6PD mutations in G6PD-deficient Egyptian children. Lab. Med., 42: 355-360.
    CrossRef  |  Direct Link  |  
  31. Sadek, H.A., B.A. Madkour, I.A. Shaheen, A.F. Saleh, R.F. Yaseen, E. El-Din A. Bayoumi and S.M. Toima, 2010. Portal vein thrombosis and haematemesis in chronic liver disease. Are P-selectin and PSGL-1 clues? Arab J. Gastroenterol., 11: 124-129.
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  32. Abdel-Raouf Afifi, R., D.K. Ali and I. Abdel-Mohsen Shaheen, 2010. A localized case-control study of extra-gastric manifestations of helicobacter pylori infection in children. Indian J. Pediatr., 78: 418-422.
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  33. El-Ainin, A.A., W. El-Metnawy, F. Haggag, N. El-Dossoki, D. Soliman, R. Afifi and I.A. Shaheen, 2009. A prospective study for the assessment of gene dysregulation in B-cell oncogenisis using complementary DNA microarray. Med. J. Cairo Univ., 77: 583-589.
  34. Khorshied, M., H. Gouda, I.A. Mohsen, M. Sroor and T.N. AL-Bolkeny, 2008. Expression and clinical implication of ZAP-70 in acute lymphoblastic leukemia. J. Medical Sci., 8: 461-468.
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  35. El-Guindy, N.M., M. Khorshied, H. Gouda, I.A. Shaheen, R.E. Abu Khalil, M. Sroor and T.N. Al-Bolkeny, 2008. The clinical relevance of Cyclin A1 over expression in acute Myeloid Leukemia. The Egyp. J. Haematol., 33: 362-369.