| Molecular Diagnosis of Glycogen storage disease type I: A review Z Beyzaei, B Geramizadeh | 30 | 2019 |
| De Novo Donor Specific Antibody and Long-Term Outcome After Liver Transplantation: A Systematic Review and Meta-Analysis Z Beyzaei, B Geramizadeh, Z Bagheri, S Karimzadeh, A Shojazadeh Frontiers in Immunology 11, 613128, 2020 | 29 | 2020 |
| Response of nitrate reductase to exogenous application of 5-aminolevulinic acid in barley plants Z Beyzaei, RA Sherbakov, NG Averina Journal of plant growth regulation 33, 745-750, 2014 | 26 | 2014 |
| Diagnosis of hepatic glycogen storage disease patients with overlapping clinical symptoms by massively parallel sequencing: a systematic review of literature Z Beyzaei, B Geramizadeh, S Karimzadeh Orphanet Journal of Rare Diseases 15, 1-13, 2020 | 25 | 2020 |
| Involvement of nitrate reductase in the ameliorating effect of 5-aminolevulinic acid on NaCl-stressed barley seedlings Z Beyzaei, NG Averina, RA Sherbakov Acta physiologiae plantarum 37, 1-8, 2015 | 21 | 2015 |
| Role of nitrogen metabolism in the development of salt tolerance in barley plants NG Averina, Z Beyzaei, RA Shcherbakov, AV Usatov Russian journal of plant physiology 61, 97-104, 2014 | 20 | 2014 |
| Quercetin can inhibit angiogenesis via the down regulation of MALAT1 and MIAT LncRNAs in human umbilical vein endothelial cells S Esteghlal, MJ Mokhtari, Z Beyzaei International journal of preventive medicine 12, 2021 | 19 | 2021 |
| Association between polymorphisms in DNA repair genes (XRCC1 and XRCC7) and risk of preeclampsia I Saadat, Z Beyzaei, F Aghaei, S Kamrani, M Saadat Archives of gynecology and obstetrics 286, 1459-1462, 2012 | 16 | 2012 |
| Liver transplantation in glycogen storage disease: a single-center experience Z Beyzaei, A Shamsaeefar, K Kazemi, S Nikeghbalian, A Bahador, ... Orphanet Journal of Rare Diseases 17 (1), 127, 2022 | 13 | 2022 |
| Clinical and genetic spectrum of glycogen storage disease in Iranian population using targeted gene sequencing Z Beyzaei, F Ezgu, B Geramizadeh, MH Imanieh, M Haghighat, ... Scientific reports 11 (1), 7040, 2021 | 12 | 2021 |
| The role of regulatory T cells in liver transplantation Z Beyzaei, A Shojazadeh, B Geramizadeh Transplant Immunology 70, 101512, 2022 | 10 | 2022 |
| The mutation spectrum and ethnic distribution of Wilson disease, a review Z Beyzaei, A Mehrzadeh, N Hashemi, B Geramizadeh Molecular Genetics and Metabolism Reports 38, 101034, 2024 | 5 | 2024 |
| Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature Z Beyzaei, F Ezgu, B Geramizadeh, A Alborzi, A Shojazadeh BMC pediatrics 21, 1-5, 2021 | 4 | 2021 |
| Novel PRKAG2 variant presenting as liver cirrhosis: report of a family with 2 cases and review of literature Z Beyzaei, F Ezgu, B Geramizadeh, A Alborzi, A Shojazadeh BMC medical genomics 14, 1-5, 2021 | 4 | 2021 |
| MOLECULAR MECHANISMS OF REGULATION OF NINRATE REDUCTASE WITH EXOGENOUS 5-AMINOLEVULINIC ACID IN BARLEY SEEDLINGS GROWN UNDER SALINIZATION WITH NaCl NG Averina, Z BEYZAEI, A SHERBAKOV Doklady of the National Academy of Sciences of Belarus 59 (4), 95-101, 2016 | 4 | 2016 |
| Association between VNTR polymorphism in promoter region of XRCC5 and susceptibility to acute lymphoblastic leukemia risk Z Beyzaei, Z Somaghi, B Geramizadeh Gene Reports 16, 100422, 2019 | 3 | 2019 |
| The mutation spectrum and ethnic distribution of non-hepatorenal tyrosinemia (types II, III) Z Beyzaei, S Nabavizadeh, S Karimzadeh, B Geramizadeh Orphanet Journal of Rare Diseases 17 (1), 424, 2022 | 2 | 2022 |
| Association between genetic polymorphism of XRCC7 (G6721T) and risk of acute lymphoblastic leukemia F Farokhian, Z Beyzaei, M Ramzi, B Geramizadeh Egyptian Journal of Medical Human Genetics 21, 1-4, 2020 | 2 | 2020 |
| Exogenous 5-‐aminolevulinic acid increases the expression of Nar1 gene and nitrate reductase protein accumulation in barley seedlings. Z Beyzaei, RA Sherbakov, NG Averina Journal of Medical & Biological Sciences, 2014 | 2 | 2014 |
| Identification of a novel mutation in the ALDOB gene in hereditary fructose intolerance Z Beyzaei, F Ezgu, MH Imanieh, M Haghighat, SM Dehghani, N Honar, ... Journal of Pediatric Endocrinology and Metabolism 36 (3), 331-334, 2023 | 1 | 2023 |
Bita GeramizadehProfessor of Pathology, Shiraz University of Medical SciencesVerified email at sums.ac.ir
