| 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 | 19 | 2019 |
| 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 | 15 | 2016 |
| 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 | 14 | 2014 |
| 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 | 8 | 2015 |
| 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 | 5 | 2019 |
| 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 | 4 | 2017 |
| 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 | 1 | 2022 |
| Prevalence of JAK2 V617F Mutation in Iranian Patients with Myeloproliferative Neoplasms H Mohammad, S Zahra Archives of Medical Laboratory Sciences 6, 1-7, 2020 | 1 | 2020 |
| Mutations in COL6A Gene Family Responsible for Muscular Dystrophies in Three Unrelated Families S Zeinali, N Soltani, Z Shahbazi, M Karimipoor, MS Fallah, ... Iranian Biomedical Journal 28 (4), 8-8, 2024 | | 2024 |
| 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 25 (5), 339-342, 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 |
Mohammad HamidAssociate Professor of Molecular Genetics (Medical) Pasteur Institute of Iran在 pasteur.ac.ir 的电子邮件经过验证
