| Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations R Alibakhshi, R Kianishirazi, JJ Cassiman, M Zamani, H Cuppens Journal of cystic fibrosis 7 (2), 102-109, 2008 | 101 | 2008 |
| Mutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations R Alibakhshi, K Moradi, Z Mohebbi, K Ghadiri Metabolic brain disease 29, 131-138, 2014 | 43 | 2014 |
| Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease A Vaisi-Raygani, H Ghaneialvar, Z Rahimi, H Tavilani, T Pourmotabbed, ... Molecular biology reports 38, 5421-5428, 2011 | 40 | 2011 |
| Detection of SPG20 gene promoter-methylated DNA, as a novel epigenetic biomarker, in plasma for colorectal cancer diagnosis using the MethyLight method N Rezvani, R Alibakhshi, A Vaisi‑Raygani, H Bashiri, M Saidijam Oncology letters 13 (5), 3277-3284, 2017 | 30 | 2017 |
| Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in Phenylketonuria patients in Western Iran K Moradi, R Alibakhshi, K Ghadiri, SR Khatami, H Galehdari Indian journal of human genetics 18 (3), 290, 2012 | 28 | 2012 |
| Mutation analysis of CFTR gene in 70 Iranian cystic fibrosis patients RAM Zamani Iranian Journal of Allergy, Asthma and Immunology, 3-8, 2006 | 28 | 2006 |
| Spectrum of phenylalanine hydroxylase gene mutations in Hamadan and Lorestan provinces of Iran and their associations with variable number of tandem repeat alleles R Alibakhshi, K Moradi, M Biglari, S Shafieenia Iranian journal of medical sciences 43 (3), 318, 2018 | 21 | 2018 |
| The Spectrum of α-Thalassemia Mutations in Kermanshah Province, West Iran R Alibakhshi, M Mehrabi, L Omidniakan, S Shafieenia Hemoglobin 39 (6), 403-406, 2015 | 19 | 2015 |
| The spectrum of β-thalassemia mutations in Kermanshah Province in West Iran and its association with hematological parameters M Mehrabi, R Alibakhshi, S Fathollahi, MR Farshchi Hemoglobin 37 (6), 544-552, 2013 | 18 | 2013 |
| The spectrum of α-thalassemia mutations in the Lak population of Iran K Moradi, M Aznab, S Tahmasebi, Z Dastafkan, L Omidniakan, M Ahmadi, ... Hemoglobin 43 (2), 107-111, 2019 | 17 | 2019 |
| Mutation analysis of exons 10 and 17a of CFTR gene in patients with cystic fibrosis in Kermanshah province, western Iran A Sahami, R Alibakhshi, K Ghadiri, H Sadeghi Journal of Reproduction & Infertility 15 (1), 49, 2014 | 14 | 2014 |
| The spectrum of β-thalassemia mutations in Hamadan Province, West Iran R Alibakhshi, K Moradi, M Aznab, A Azimi, S Shafieenia, M Biglari Hemoglobin 43 (1), 18-22, 2019 | 13 | 2019 |
| High risk of birth defects with PKU in Mast-e Ali village, Kermanshah province K Moradi, R Alibakhshi Journal of Kermanshah University of Medical Sciences 18 (1), 2014 | 13 | 2014 |
| Association between activity and genotypes of paraoxonase1 L55M (rs854560) increases the disease activity of rheumatoid arthritis through oxidative stress M Tanhapour, S Shahmohamadnejad, A Vaisi-Raygani, A Kiani, ... Molecular biology reports 46, 741-749, 2019 | 12 | 2019 |
| Cytogenetic analysis of 570 couples with recurrent pregnancy loss: reporting 11 years of experience R Alibakhshi, P Nejati, S Hamani, N Mir-Ahadi, N Jalilian Journal of Human Reproductive Sciences 13 (3), 216-220, 2020 | 11 | 2020 |
| The proportion of tetrahydrobiopterin deficiency and PAH gene deficiency variants among cases with hyperphenyalaninemia in Western Iran K Moradi, R Alibakhshi, S Khatami Indian journal of human genetics 19 (4), 454, 2013 | 11 | 2013 |
| Spectrum of PAH gene mutations in 1547 phenylketonuria patients from Iran: a comprehensive systematic review R Alibakhshi, A Mohammadi, N Salari, S Khamooshian, M Kazeminia, ... Metabolic brain disease 36 (5), 767-780, 2021 | 10 | 2021 |
| CFTR mutation analysis in Western Iran: identification of two novel mutations N Karimi, R Alibakhshi, S Almasi Journal of Reproduction & Infertility 19 (1), 3, 2018 | 10 | 2018 |
| α-thalassemia mutations in Ilam Province, West Iran K Moradi, M Aznab, A Azimi, M Biglari, S Shafieenia, R Alibakhshi Hemoglobin 46 (3), 147-152, 2022 | 9 | 2022 |
| CFTR gene mutation spectrum among 735 Iranian patients with cystic fibrosis: A comprehensive systematic review R Alibakhshi, A Mohammadi, S Khamooshian, M Kazeminia, K Moradi Pediatric pulmonology 56 (12), 3644-3656, 2021 | 9 | 2021 |
Keivan MoradiKermanshah University of Medical Sciences在 kums.ac.ir 的电子邮件经过验证
