| Molecular mechanisms of apoptosis and roles in cancer development and treatment S Goldar, MS Khaniani, SM Derakhshan, B Baradaran Asian Pacific journal of cancer prevention 16 (6), 2129-2144, 2015 | 746 | 2015 |
| Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism DZ Loesch, MS Khaniani, HR Slater, JP Rubio, QM Bui, K Kotschet, ... Clinical genetics 76 (5), 471-476, 2009 | 77 | 2009 |
| An improved diagnostic PCR assay for identification of cryptic heterozygosity for CGG triplet repeat alleles in the fragile X gene (FMR1) MS Khaniani, P Kalitsis, T Burgess, HR Slater Molecular Cytogenetics 1, 1-6, 2008 | 66 | 2008 |
| Simultaneous downregulation of miR‐21 and miR‐155 through oleuropein for breast cancer prevention and therapy M Abtin, MR Alivand, MS Khaniani, M Bastami, M Zaeifizadeh, ... Journal of cellular biochemistry 119 (9), 7151-7165, 2018 | 51 | 2018 |
| Inhibition of MEK/ERK1/2 signaling affects the fatty acid composition of HepG2 human hepatic cell line B Yousefi, M Darabi, B Baradaran, MS Khaniani, M Rahbani, M Darabi, ... BioImpacts: BI 2 (3), 145, 2012 | 51 | 2012 |
| Downregulation of HDAC2 and HDAC3 via oleuropein as a potent prevention and therapeutic agent in MCF‐7 breast cancer cells S Bayat, S Mansoori Derakhshan, N Mansoori Derakhshan, ... Journal of cellular biochemistry 120 (6), 9172-9180, 2019 | 47 | 2019 |
| HDACis (class I), cancer stem cell, and phytochemicals: Cancer therapy and prevention implications S Bayat, MS Khaniani, J Choupani, MR Alivand, SM Derakhshan Biomedicine & Pharmacotherapy 97, 1445-1453, 2018 | 47 | 2018 |
| Narrower insight to SIRT1 role in cancer: A potential therapeutic target to control epithelial–mesenchymal transition in cancer cells J Choupani, S Mansoori Derakhshan, S Bayat, MR Alivand, ... Journal of cellular physiology 233 (6), 4443-4457, 2018 | 46 | 2018 |
| RIT2 Polymorphisms: Is There a Differential Association? B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, MS Khaniani, ... Molecular neurobiology 54, 2234-2240, 2017 | 39 | 2017 |
| The HLA-G 14-bp insertion/deletion polymorphism in recurrent spontaneous abortion among Iranian women F Afkhami, MS Khaniani, L Farzadi, Z Paknejad, SM Derakhshan Iranian Journal of Allergy, Asthma and Immunology, 364-369, 2014 | 39 | 2014 |
| A new insight on serum microRNA expression as novel biomarkers in breast cancer patients Z Bahmanpour, R Sheervalilou, J Choupani, M Shekari Khaniani, ... Journal of Cellular Physiology 234 (11), 19199-19211, 2019 | 37 | 2019 |
| An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population T Ghasemnejad, MS Khaniani, F Zarei, M Farbodnia, SM Derakhshan International journal of pediatric otorhinolaryngology 97, 113-126, 2017 | 35 | 2017 |
| HLA‐G regulatory variants and haplotypes with susceptibility to recurrent pregnancy loss N Yazdani, M Shekari Khaniani, M Bastami, T Ghasemnejad, F Afkhami, ... International Journal of Immunogenetics 45 (4), 181-189, 2018 | 32 | 2018 |
| NUCB2/Nesfatin-1: a potent meal regulatory hormone and its role in diabetes S Khalili, MS Khaniani, F Afkhami, SM Derakhshan Egyptian Journal of Medical Human Genetics 18 (2), 105-109, 2017 | 31 | 2017 |
| PPARγ agonist-induced alterations in Δ6-desaturase and stearoyl-CoA desaturase 1: Role of MEK/ERK1/2 pathway N Saliani, M Darabi, B Yousefi, B Baradaran, MS Khaniani, M Darabi, ... World journal of hepatology 5 (4), 220, 2013 | 29 | 2013 |
| Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms DZ Loesch, DE Godler, M Khaniani, E Gould, G Freya, C Dissanayake, ... American journal of medical genetics. Part A, 2306, 2009 | 29 | 2009 |
| The hopeful anticancer role of oleuropein in breast cancer through histone deacetylase modulation N Mansouri, MR Alivand, S Bayat, MS Khaniani, SM Derakhshan Journal of Cellular Biochemistry 120 (10), 17042-17049, 2019 | 20 | 2019 |
| The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population N Shahmohammadibeni, S Rahimi-Aliabadi, J Jamshidi, ... Neurological Sciences 37, 731-736, 2016 | 17 | 2016 |
| Prenatal diagnosis of spinal muscular atrophy: clinical experience and molecular genetics of SMN gene analysis in 36 cases MS Khaniani, SM Derakhshan, S Abasalizadeh Journal of prenatal medicine 7 (3), 32, 2013 | 17 | 2013 |
| Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population F Madadi, MS Khaniani, EE Shandiz, H Ayromlou, S Najmi, ... Genetic testing and molecular biomarkers 20 (10), 629-632, 2016 | 16 | 2016 |
Sima Mansoori DerakhshanTabriz university of medical sciencesDirección de correo verificada de tbzmed.ac.ir