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Fatemeh Azimi
Fatemeh Azimi
Iran University of Medical Sciences
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Year
Frequency of ITPA gene polymorphisms in Iranian patients with acute lymphoblastic leukemia and prediction of its myelosuppressive effects
F Azimi, Y Mortazavi, S Alavi, M Khalili, A Ramazani
Leukemia research 39 (10), 1048-1054, 2015
232015
Assessment of Thiopurine-based drugs according to Thiopurine S-methyltransferase genotype in patients with Acute Lymphoblastic Leukemia.
F Azimi, M Jafariyan, S Khatami, Y Mortazavi, M Azad
Iran J Ped Hematol Oncol 4 (1), 32-8, 2014
162014
Global incidence and trend of uveal melanoma from 1943-2015: A meta-analysis
M Naseripour, F Azimi, R Mirshahi, G Khakpour, A Pourhoseingholi, ...
Asian Pacific Journal of Cancer Prevention: APJCP 23 (5), 1791, 2022
112022
Young breast cancer: novel gene methylation in WBC
M Noruzinia, J Tavakkoly-Bazzaz, M Ahmadvand, F Azimi, ...
Asian Pacific Journal of Cancer Prevention: APJCP 22 (8), 2371, 2021
52021
New horizons in retinoblastoma treatment: an updated review article
F Azimi, R Mirshahi, M Naseripour
Molecular Vision 28, 130, 2022
42022
Spotlight on targeted chemotherapy in retinoblastoma: Safety, efficacy, and patient outcomes
M Naseripour, R Mirshahi, H Kasraei, A Sedaghat, F Azimi
OncoTargets and Therapy 15, 1545, 2022
32022
Role of Glutathione S-transferase (GSTM1, GSTT1) and CYP1A1 (cytochrome p450) Gene polymorphisms in susceptibility to acute myeloid leukemia
Y Mortazavi, R Rahimi, F Azimi, S Rostami, M Moghimi, S Faghihzadeh, ...
Middle East Journal of Cancer 11 (1), 12-20, 2020
32020
Association of RB1 rs9568036 and CDKN1A rs1801270 polymorphisms with retinoblastoma susceptibility
F Azimi, M Naseripour, A Sedaghat, ZA Kachoei, G Khakpoor
Journal of Current Ophthalmology 34 (3), 328-332, 2022
12022
Investigation of germline VHL variants in Iranian patients with retinal capillary hemangioblastoma and genotype-phenotype analysis
M Naseripour, F Azimi, S Talebi, R Mirshahi, R Kiaee, A Sedaghat, ...
Ophthalmic Genetics 44 (3), 211-217, 2023
2023
A meta-analysis of different von Hippel Lindau mutations: are they related to retinal capillary hemangioblastoma?
F Azimi, A Aghajani, G Khakpour, S Chaibakhsh
Molecular Genetics and Genomics 297 (6), 1615-1626, 2022
2022
In Silico Analysis of Novel VHL Germline Mutations in Iranian RCH Patients
M Naseripour, K Bagherzadeh, G Khakpoor, A Sedaghat, R Mirshahi, ...
bioRxiv, 2022.10. 26.513811, 2022
2022
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