| Ataxia‐telangiectasia: A review of clinical features and molecular pathology P Amirifar, MR Ranjouri, R Yazdani, H Abolhassani, A Aghamohammadi Pediatric Allergy and Immunology 30 (3), 277-288, 2019 | 172 | 2019 |
| Ataxia-telangiectasia: epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management P Amirifar, MR Ranjouri, M Lavin, H Abolhassani, R Yazdani, ... Expert review of clinical immunology 16 (9), 859-871, 2020 | 39 | 2020 |
| Effect of class switch recombination defect on the phenotype of ataxia-telangiectasia patients P Amirifar, H Mozdarani, R Yazdani, F Kiaei, T Moeini Shad, ... Immunological Investigations 50 (2-3), 201-215, 2021 | 28 | 2021 |
| Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): a systematic review P Amirifar, MR Ranjouri, H Abolhassani, T Moeini Shad, ... Pediatric Allergy and Immunology 32 (1), 186-197, 2021 | 19 | 2021 |
| Variable abnormalities in T and B cell subsets in ataxia telangiectasia T Moeini Shad, B Yousefi, P Amirifar, S Delavari, W Rae, P Kokhaei, ... Journal of clinical immunology 41, 76-88, 2021 | 18 | 2021 |
| Known and potential molecules associated with altered B cell development leading to predominantly antibody deficiencies P Amirifar, R Yazdani, G Azizi, MR Ranjouri, A Durandy, A Plebani, ... Pediatric Allergy and Immunology 32 (8), 1601-1615, 2021 | 14 | 2021 |
| Atypical ataxia presentation in variant ataxia telangiectasia: Iranian case-series and review of the literature T Moeini Shad, R Yazdani, P Amirifar, S Delavari, M Heidarzadeh Arani, ... Frontiers in Immunology 12, 779502, 2022 | 12 | 2022 |
| Cutaneous granulomatosis and class switching defect as a presenting sign in ataxia-telangiectasia: first case from the national Iranian registry and review of the literature P Amirifar, R Yazdani, T Moeini Shad, A Ghanadan, H Abolhassani, ... Immunological Investigations 49 (6), 597-610, 2020 | 10 | 2020 |
| Association study of IL2RA and CTLA4 gene variants with type I diabetes mellitus in children in the northwest of Iran MR Ranjouri, P Aob (Amirifar), SM Derakhshan, MS Khaniani, H Chiti, ... BioImpacts: BI 6 (4), 187, 2016 | 6 | 2016 |
| The role of Motin family proteins in tumorigenesis—an update P Amirifar, J Kissil Oncogene, 1-7, 2023 | 5 | 2023 |
| The spectrum of ATM gene mutations in Iranian patients with ataxia‐telangiectasia P Amirifar, MR Ranjouri, S Pashangzadeh, M Lavin, R Yazdani, ... Pediatric Allergy and Immunology 32 (6), 1316-1326, 2021 | 5 | 2021 |
| Molecular analysis and prevalence of Huntington disease in northwestern Iran MS Khaniani, P Aob (Amirifar), M Ranjouri, SM DERAKHSHAN Turkish Journal of Medical Sciences 47 (6), 1880-1884, 2017 | 4 | 2017 |
| Clinical Manifestations in Iranian Ataxia Telangiectasia Patients T Moeini Shad, MR Ranjouri, P Amirifar Immunology and Genetics Journal 3 (1), 29-40, 2020 | 2 | 2020 |
| NC13D deficiency associated with epileptic seizures and antibody deficiency: the first case from the Iranian National Registry R Yazdani, P Amirifar, H Abolhassani, G Azizi, N Parvaneh, N Rezaei, ... J. investig. allergol. clin. immunol, 160-162, 2019 | 2 | 2019 |
| Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients P Amirifar, M Mehrmohamadi, MR Ranjouri, SM Akrami, N Rezaei, ... Journal of Clinical Immunology, 1-13, 2022 | | 2022 |
| The Origins of the First Reported Cases of the Primary Immunodeficiency Diseases SE Rasouli, P Amirifar Immunology and Genetics Journal, 2021 | | 2021 |
Joseph KissilThe Moffitt Cancer Center
Joseph KissilThe Moffitt Cancer Center