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Oncogene|March 27, 2023
The role of Motin family proteins in tumorigenesis-an updateParisa Amirifar, Joseph KissilCancer Treatment and Research Communications|August 7, 2026
CRISPR-Cas9 gene editing approaches in colorectal cancer: Current progress and future prospectsMohadeseh Hassannia, Parisa AmirifarEpigenomics|June 11, 2026
DNA methylation in glioblastoma: insights from single-cell epigenomicsRana Zohreh, Nima Rezaei, Parisa AmirifarPediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|January 28, 2019
Ataxia-telangiectasia: A review of clinical features and molecular pathologyParisa Amirifar, Mohammad Reza Ranjouri, Reza Yazdani, et al.Expert Review of Clinical Immunology|August 15, 2020
Ataxia-telangiectasia: epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and managementParisa Amirifar, Mohammad Reza Ranjouri, Martin Lavin, et al.Immunological Investigations|November 26, 2019
Cutaneous Granulomatosis and Class Switching Defect as a Presenting Sign in Ataxia-Telangiectasia: First Case from the National Iranian Registry and Review of the LiteratureParisa Amirifar, Reza Yazdani, Tannaz Moeini Shad, et al.Journal of Clinical Immunology|October 14, 2020
Variable Abnormalities in T and B Cell Subsets in Ataxia TelangiectasiaTannaz Moeini Shad, Bahman Yousefi, Parisa Amirifar, et al.Journal of Clinical Immunology|October 10, 2021
Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia PatientsParisa Amirifar, Mahya Mehrmohamadi, Mohammad Reza Ranjouri, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|June 28, 2021
Known and potential molecules associated with altered B cell development leading to predominantly antibody deficienciesParisa Amirifar, Reza Yazdani, Gholamreza Azizi, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|July 18, 2020
Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic reviewParisa Amirifar, Mohammad Reza Ranjouri, Hassan Abolhassani, et al.Pageof 2