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zahra shahbazi
zahra shahbazi
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Cited by
Cited by
Year
Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran
Z Shahbazi, R Yazdani, S Shahkarami, S Shahbazi, M Hamid, ...
Immunology letters 216, 70-78, 2019
172019
Association study of rs1333040 and rs1004638 polymorphisms in the 9p21 locus with coronary artery disease in Southwest of Iran
KG Khademi, AM Foroughmand, H Galehdari, S Yazdankhah, ...
Iranian biomedical journal 20 (2), 122, 2016
142016
Association of MEF2A gene polymorphisms with coronary artery disease
AM Foroughmand, Z Shahbazi, H Galehdari, MP Borujeni, P Dinarvand, ...
Iranian Red Crescent Medical Journal 16 (8), 2014
142014
SULF 1 gene polymorphism, rs6990375 is in significant association with fetus failure in IVF technique
E Taghizadeh, SM Kalantar, R Mahdian, MH Sheikhha, E Farashahi-Yazd, ...
Iranian journal of reproductive medicine 13 (4), 215, 2015
82015
Graft versus host disease and microchimerism in a JAK3 deficient patient
RM Zahra Shahbazi, Nima Parvaneh, Shirin Shahbazi, Hamzeh Rahimi, Mohammad ...
Allergy, Asthma & Clinical Immunology 15 (47), 1-9, 2019
52019
Association study of leptin and leptin receptor gene polymorphisms with diabetes type 2 and obesity
H Taghizadeh, H Abdolkarimi, H Bazireh, R Houshmand, Z Shahbazi, ...
Health Biotechnol Biopharma 1, 61-69, 2017
42017
Prevalence of JAK2 V617F Mutation in Iranian Patients with Myeloproliferative Neoplasms
H Mohammad, S Zahra
Archives of Medical Laboratory Sciences 6, 1-7, 2020
12020
Homozygosity for Robertsonian Translocation (14q; 15q) in a Newborn with a Familial History of Recurrent Abortion and Newborns Affected by Hepatosplenomegaly: A Case Report
S Sahraeean, A Jebelli, Z Shahbazi, F Piryaei
Journal of Reproduction & Infertility 24 (4), 301, 2023
2023
A de novo TINF2, R282C Mutation in a Case of Dyskeratosis Congenital Founded by Next-Generation Sequencing
M Khakzad, Z Shahbazi, M Naderi, M Karimipoor
Iranian biomedical journal 27 (2-3), 146, 2023
2023
Hb Narges Lab, a Novel Hemoglobin Variant of the β-Globin Gene.
M Hamid, Z Shahbazi, B Keikhaei, H Galehdari, A Saberi, A Sedaghat, ...
Archives of Iranian Medicine (AIM) 25 (5), 2022
2022
New heritable ATRX mutation identified by whole exome sequencing and review
Z Shahbazi, G Rostami, M Hamid
Egyptian Journal of Medical Human Genetics 23 (1), 19, 2022
2022
Distribution of Disease-Causing Mutations through Different Protein Domains in Patients with Severe Combined Immunodeficiency
S Zahra, S Shirin, R Hamzeh, M Reza
Archives of Medical Laboratory Sciences 5 (4), 1-7, 2020
2020
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