| High-throughput bioaccumulation, biotransformation, and production of silver and selenium nanoparticles using genetically engineered Pichia pastoris F Elahian, S Reiisi, A Shahidi, SA Mirzaei Nanomedicine: Nanotechnology, Biology and Medicine 13 (3), 853-861, 2017 | 94 | 2017 |
| miRNAs, oxidative stress, and cancer: A comprehensive and updated review SO Ebrahimi, S Reiisi, S Shareef Journal of cellular physiology 235 (11), 8812-8825, 2020 | 51 | 2020 |
| Aloe vera toxic effects: expression of inducible nitric oxide synthase (iNOS) in testis of Wistar rat S Asgharzade, M Rafieian-Kopaei, A Mirzaeian, S Reiisi, L Salimzadeh Iranian journal of basic medical sciences 18 (10), 967, 2015 | 46 | 2015 |
| Downregulation of miR-4443 and miR-5195-3p in ovarian cancer tissue contributes to metastasis and tumorigenesis SO Ebrahimi, S Reiisi Archives of gynecology and obstetrics 299, 1453-1458, 2019 | 43 | 2019 |
| Design, synthesis, and anti-gastric cancer activity of novel 2, 5-diketopiperazine S Farhadian, B Shareghi, F Tirgir, S Reiisi, NG Dehkordi, L Momeni, ... Journal of Molecular Liquids 294, 111585, 2019 | 42 | 2019 |
| Isolation, culture and identification of epidermal stem cells from newborn mouse skin S Reiisi, F Esmaeili, A Shirazi In Vitro Cellular & Developmental Biology-Animal 46, 54-59, 2010 | 42 | 2010 |
| Broad blocking of MDR efflux pumps by acetylshikonin and acetoxyisovalerylshikonin to generate hypersensitive phenotype of malignant carcinoma cells SA Mirzaei, S Reiisi, P Ghiasi Tabari, A Shekari, F Aliakbari, E Azadfallah, ... Scientific Reports 8 (1), 3446, 2018 | 37 | 2018 |
| GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants M Koohiyan, M Hashemzadeh-Chaleshtori, M Salehi, H Abtahi, S Reiisi, ... International Journal of Pediatric Otorhinolaryngology 107, 121-126, 2018 | 31 | 2018 |
| Association between Helicobacter pylori cagA, babA2 virulence factors and gastric mucosal interleukin-33 mRNA expression and clinical outcomes in dyspeptic patients H Shahi, S Reiisi, R Bahreini, N Bagheri, L Salimzadeh, H Shirzad International Journal of Molecular and Cellular Medicine 4 (4), 227, 2015 | 29 | 2015 |
| Regulatory and immunomodulatory role of miR-34a in T cell immunity F Taheri, SO Ebrahimi, S Shareef, S Reiisi Life Sciences, 118209, 2020 | 26 | 2020 |
| Study of correlation between genetic variants in three microRNA genes (hsa-miR-146a, hsa-miR-502 binding site, hsa-miR-27a) and breast cancer risk SP Barjui, S Reiisi, SO Ebrahimi, B Shekari Current research in translational medicine 65 (4), 141-147, 2017 | 18 | 2017 |
| A novel TECTA mutation causes ARNSHL S Asgharzade, MA Tabatabaiefar, MH Modarressi, MH Ghahremani, ... International Journal of Pediatric Otorhinolaryngology 92, 88-93, 2017 | 16 | 2017 |
| Increased risk of polycystic ovary syndrome (PCOS) associated with CC genotype of miR-146a gene variation SO Ebrahimi, S Reiisi, S Parchami Barjui Gynecological Endocrinology 34 (9), 793-797, 2018 | 15 | 2018 |
| The study of SLC26A4 gene causing autosomal recessive hearing loss by linkage analysis in a cohort of Iranian populations S Reiisi, MH Sanati, MA Tabatabaiefar, S Ahmadian, S Reiisi, S Parchami, ... International journal of molecular and cellular medicine 3 (3), 176, 2014 | 15 | 2014 |
| Human glutathione s-transferase enzyme gene variations and risk of multiple sclerosis in Iranian population cohort SP Barjui, S Reiisi Multiple sclerosis and related disorders 17, 41-46, 2017 | 13 | 2017 |
| Screening of Myo7A mutations in Iranian patients with autosomal recessive hearing loss from west of Iran S Asgharzade, S Reiisi, MA Tabatabaiefar, MH Chaleshtori Iranian journal of public health 46 (1), 76, 2017 | 13 | 2017 |
| Mutation in second exon of myo15a gene cause of nonsyndromic hearing loss and its association in the Arab population in Iran S Asgharzade, MH Chaleshtori, MA Tabatabaifar, S Reisi, MH Modaressi Genetika 48 (2), 587-596, 2016 | 12 | 2016 |
| Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a … S Reiisi, MA Tabatabaiefar, MH Sanati, MH Chaleshtori Iranian journal of basic medical sciences 19 (7), 772, 2016 | 11 | 2016 |
| Prevalence of cagA and babA2 genes in Helicobacter pylori strains isolated from Iranian gastrointestinal disorder patients and their gastritis classification. H Shahi, S Reiisi, M Sadeghiani, M Mahsa, R Bahreini, M Moghni, ... Journal of Biology and Today's World 3 (12), 256-260, 2014 | 10 | 2014 |
| Association between H. pylori babA virulence factor with clinical outcome and ABO blood groups H Shahi, M Moghni, R Bahreini, S Reiisi, M Sadeghiani, M Rahimi, ... JPAM 9, 285-90, 2015 | 9 | 2015 |
seyed omar ebrahimiMSc of geneticVerified email at stu.sku.ac.ir
