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BMC Medical Genetics|February 14, 2020
Association of IL-10 gene promoter polymorphisms with susceptibility to pseudoexfoliation syndrome, pseudoexfoliative and primary open-angle glaucomaGhasem Fakhraie, Farshid Parvini, Jalaledin Ghanavi, et al.Current Microbiology|April 13, 2021
Characterization of Clinical Isolates of Mycobacterium simiae Using Drug Susceptibility Tests and Molecular AnalysesHoda Dezhkhi, Parissa Farnia, Azam Haddadi, et al.The American Journal of Tropical Medicine and Hygiene|July 19, 2017
Association of Interferon-<i>γ</i> Receptor-1 Gene Polymorphism with Nontuberculous Mycobacterial Lung Infection among Iranian Patients with Pulmonary DiseasePoopak Farnia, Jalaledin Ghanavi, Shima Saif, et al.International Journal of Mycobacteriology|January 4, 2017
The importance of single nucleotide polymorphisms in interferon gamma receptor-1 gene in pulmonary patients infected with rapid grower mycobacteriumPoopak Farnia, Jalaledin Ghanavi, Payam Tabasri, et al.Tuberculosis and Respiratory Diseases|October 30, 2020
An Overview of Genetic Information of Latent Mycobacterium tuberculosisFaezeh Hamidieh, Parissa Farnia, Jamileh Nowroozi, et al.Polish Journal of Radiology|March 18, 2020
Computerised tomography scan in multi-drug-resistant versus extensively drug-resistant tuberculosisPayam Mehrian, Poopak Farnia, Dina Jalalvand, et al.Tanaffos|October 19, 2022
Molecular Dynamic Simulations and Molecular Docking as a Potential Way for Designed New Inhibitor Drug without ResistanceJafar Aghajani, Poopak Farnia, Parissa Farnia, et al.International Journal of Mycobacteriology|September 15, 2024
Prevalence and Temporal Trends of Multidrug-resistant Tuberculosis in Iran from 1981 to 2023: A Systematic Review and Meta-analysisSaman Ayoubi, Parissa Farnia, Poopak Farnia, et al.International Journal of Mycobacteriology|June 25, 2024
Pharmacogenetic Study of Drugs Affecting Mycobacterium tuberculosisSamira Shabani, Poopak Farnia, Jalaledin Ghanavi, et al.The Application of Clinical Genetics|September 18, 2020
A Homozygous Truncating Mutation in <i>NALCN</i> Causing IHPRF1: Detailed Clinical Manifestations and a Review of LiteratureAmir Hossein Karimi, Mohammad Reza Karimi, Poopak Farnia, et al.Pageof 6