| Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations M Abiri, H Saei, M Eghbali, R Karamzadeh, T Shirzadeh, Z Sharifi, ... Metabolic Brain Disease 34, 1145-1156, 2019 | 16 | 2019 |
| Hepatoprotective effect of cornus mas fruits extract on serum biomarkers in methotrexate-induced liver injury in male rats H Saei, H Hatami, M Azarmi, G Dehghan Pharmacologyonline 1, 91-98, 2016 | 11 | 2016 |
| Comprehensive transcriptome mining identified the gene expression signature and differentially regulated pathways of the late-onset preeclampsia H Saei, A Govahi, A Abiri, M Eghbali, M Abiri Pregnancy Hypertension 25, 91-102, 2021 | 9 | 2021 |
| Whole-exome sequencing uncovers novel causative variants and additional findings in three patients affected by glycogen storage disease type VI and Fanconi− Bickel syndrome M Eghbali, KS Fatemi, S Salehpour, M Abiri, H Saei, S Talebi, NA Olyaei, ... Frontiers in Genetics 11, 601566, 2021 | 9 | 2021 |
| Hepatoprotective effect of ethanolic extract of Lavandula officinalis L. in alloxan-induced diabetic rats H Saei, M Azarmi, G Dehghan, SZ Salmasi, S Zeinali Thrita 5 (2), 2016 | 4 | 2016 |
| Investigating the Treatable Effect of Lavandula officinalis L. Ethanolic Extract in Alloxan-Induced Male Diabetic Rats M Azarmi, H Saei, S Zehtab Salmasi, G Dehghan Pharmacol. Line 1, 53-63, 2016 | 4 | 2016 |
| A wave of deep intronic mutations in X-linked Alport syndrome M Boisson, C Arrondel, N Cagnard, V Morinière, ZA Arkoub, H Saei, ... Kidney International 104 (2), 367-377, 2023 | 3 | 2023 |
| VNtyper enables accurate alignment-free genotyping of MUC1 coding VNTR using short-read sequencing data in autosomal dominant tubulointerstitial kidney disease H Saei, V Morinière, L Heidet, O Gribouval, S Lebbah, F Tores, ... Iscience 26 (7), 2023 | 2 | 2023 |
| Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion N Jabbarpour, B Poorshiri, H Saei, M Barzegar, M Bonyadi Journal of Genetics 102 (1), 18, 2023 | 1 | 2023 |
| Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract N Jabbarpour, H Saei, MH Jabbarpoor Bonyadi, M Bonyadi Ophthalmic Genetics 43 (5), 609-614, 2022 | 1 | 2022 |
Maryam AbiriAssistant professor, Iran university of medical sciencesVerified email at iums.ac.ir
