Zahra Beyzaei

1. Bayzaei Z, Dehghani SM, Geramizadeh B. Tyrosinemia Type II. 2024 Oct 24. In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024.
2. Beyzaei Z, Goudarzi Z, Dhghani SM, Moravej H, et al. Mutation Spectrum of Tyrosinemia Type I in Iran, A Retrospective Cohort Study. European Journal of Medical Genetics. 2024;71:104970
3. Naseri R, Beyzaei Z, Geramizadeh B. Introduction of a Novel Cut-off in Newborn Screening of Galactosemia; a Cohort Study. Iranian Journal of Pediatrics. 2024; e142691
4. Beyzaei Z, Ghatei K, Geramizadeh B, et al. Liver Transplantation in Wilson Disease: A Single-Center Experience. Orphanet Journal of Rare Diseases. 2024.
5. Beyzaei Z, Moravej H, Imanieh MH, Inaloo S, Geramizadeh B. Clinical spectrum and genetic variation of six patients with methylmalonic aciduria (MMAs); A report from Iran. Molecular Genetics and Genomics. 2024;45:101023
6. Beyzaei Z, Mehrzadeh A, Hashemi N, Geramizadeh B. The mutation spectrum and ethnic distribution of Wilson disease, a review. Molecular Genetics and Metabolism Reports. 2024;38: 101034.
7. Beyzaei Z, Moravej H, Imanieh MH, Inaloo S, Geramizadeh B. Identification of two Iranian siblings with cerebrotendinous xanthomatosis: A case report. Egyptian Journal of Medical Human Genetics. 2023;24:34-39.
8. Beyzaei Z, Ezgu F, Geramizadeh B, Imanieh MH, et al. Identification of a Novel Mutation in the ALDOB Gene in Hereditary Fructose Intolerance. Journal of Pediatric Endocrinology and Metabolism. 2023;1:145-149.
9. Beyzaei Z, Geramizadeh B, Karimzadeh S. The mutation spectrum and ethnic distribution of non-hepatorenal tyrosinemia (types II, III). Orphanet Journal of Rare Diseases. 2022; 17:424.
10. Beyzaei Z, Geramizadeh B, Bagheri Z, Karimzadeh S. Outcome of liver transplantation in hepatic glycogen storage disease: A systematic review and meta-analysis. Clinical Transplantation. 2022; e14867.
11. Beyzaei Z, Shamsaeefar A, Kazemi K, Nikeghbalian S, Bahador A, Dehghani M, Malekhosseini SA, Geramizadeh B. Liver transplantation in glycogen storage disease: a single-center experience. Orphanet Journal of Rare Diseases. 2022; 17:127.
12. Beyzaei Z, Ezgu F, Geramizadeh B, Imanieh MH, et al. Clinical and genetic spectrum of glycogen storage disease and disorders in Iranian population by Targeted panel sequencing. Scientific Reports. 2021;11:7040.
13. Beyzaei Z, Ezgu F, Geramizadeh B. 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. BMC Pediatrics. 2021; 21:175-180.
14. Beyzaei Z, Ezgu F, Geramizadeh B. Novel PRKAG2 variant presenting as liver cirrhosis: Report of a family with 2 cases and review of literature. BMC Medical Genomics. 2021; 14:33-38.
15. Beyzaei Z, Ezgu F, Imanieh MH, Geramizadeh B. Identification of a novel mutation in the PHKA2 gene in a child with liver cirrhosis. Journal of Pediatric Endocrinology and Metabolism. 2021: DOI:10.1515/jpem-2021-0385
16. Beyzaei Z, Geramizadeh B. The Role of Regulatory T cells in liver transplantation. Transplant Immunology. 2021: DOI: 10.1016/j.trim.2021. 101512.
17. Pourkhosravani M, Beyzaei Z, Mokhatri MJ, Geramizadeh B. Association between polymorphism of XRCC7 and susceptibility to Varicocele risk. Gene Reports. 2021; 23:101046. (Corresponding author)
18. Esteghlal M, Mokhtari MJ, Beyzaei Z. Quercetin can inhibit angiogenesis via the downregulation of LncRNA MALAT1 in human umbilical vein endothelial cells. International Journal of Preventive Medicine. 2021; 12(1):59-64.
19. Beyzaei Z, Geramizadeh B, Karimzadeh S. Diagnosis of hepatic Glycogen Storage Disease patients with overlapping clinical symptoms by massively parallel sequencing: a systematic review of literature. Orphanet Journal of Rare Diseases. 2020; 15:286.
20. Beyzaei Z, Geramizadeh B, Bagheri Z, Karimzadeh S. De novo Donor Specific Antibody and Long Term Outcome after Liver Transplantation: A Systematic Review and Meta-analysis. Frontiers in immunology. 2020; 11:613128.
21. Farokhian F, Ramzi M, Geramizadeh B, Beyzaei Z. Association between genetic polymorphism of XRCC7 (G6721T) and acute lymphoblastic leukemia risk. Egyptian Journal of Medical Human Genetics. 2020; 21:19-23. (Corresponding author)
22. Namvaran MR, Beyzaei Z, Mokhatri MJ, Geramizadeh B. Association between polymorphism of XRCC6 and Varicocele risk. Egyptian Journal of Medical Human Genetics. 2020;21:71-76. (Corresponding author)
23. Beyzaei Z, Somaghi Z, Geramizadeh B. Association between VNTR polymorphism in the promoter region of XRCC5 and susceptibility to acute lymphoblastic leukemia risk. Gene reports. 2019;16:125-127. (Corresponding author)
24. Beyzaei Z, Geramizadeh B. Molecular Diagnosis of Glycogen storage disease type I: A review. EXCL Journal. 2019;18:30-46.
25. Beyzaei Z, Sherbakov RV, Averina NG. Involvement of nitrate reductase in the ameliorating effect of 5-aminolevulinic acid on NaCl-stressed barley seedlings. Acta Physiologiae Plantarum. 2015;37:11-20.
26. Beyzaei Z, Sherbakov RA, Averina NG. Response of nitrate reductase to exogenous application of 5-aminolevulinic acid in barley plants. Journal of Plant Growth Regulation. 2014;33(4):745-750 .
27. Averina NG, Beyzaei Z, Sherbakov RV, Usatov AA. Role of nitrogen metabolism in the development of salt tolerance in barley plants. Russian Journal of Plant Physiology. 2014;61(1):97–104.
28. Saadat I, Beyzaei Z, Aghaei F, Kamrani S, Saadat M. Association between polymorphisms in DNA repair genes (XRCC1 and XRCC7) and risk of preeclampsia. Archives of Gynecology and Obstetrics. 2012;286(6):1459-62.