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Mohsen Soosanabadi
Mohsen Soosanabadi
Staff Member of Medical Genetics, Semnan University of Medical Sciences
Verified email at semums.ac.ir
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Cited by
Cited by
Year
MicroRNA binding site polymorphism in inflammatory genes associated with colorectal cancer: literature review and bioinformatics analysis
MMPP Mohammad Reza Karimzadeh, Maryam Zarin, Naeim Ehtesham, Sharifeh ...
Cancer Gene Therapy, 2020
292020
Investigation of piwi-interacting RNA pathway genes role in idiopathic non-obstructive azoospermia
Z Kamaliyan, S Pouriamanesh, M Soosanabadi, M Gholami, ...
Scientific reports 8 (1), 142, 2018
292018
Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans
A Heidari, ZNS Fam, E Esmaeilzadeh-Gharehdaghi, M Banan, ...
Gene 492 (1), 195-198, 2012
242012
Advance trends in targeting homology-directed repair for accurate gene editing: An inclusive review of small molecules and modified CRISPR-Cas9 systems
F Shams, H Bayat, O Mohammadian, S Mahboudi, H Vahidnezhad, ...
BioImpacts: BI 12 (4), 371, 2022
212022
Three functional variants in the NLRP3 gene are associated with susceptibility and clinical characteristics of systemic lupus erythematosus
N Ehtesham, M Zare Rafie, E Esmaeilzadeh, M Dehani, S Davar, ...
Lupus 30 (8), 1273-1282, 2021
202021
Thermal inactivation of COVID‐19 specimens improves RNA quality and quantity
M Hemati, M Soosanabadi, T Ghorashi, H Ghaffari, A Vahedi, ...
Journal of Cellular Physiology 236 (7), 4966-4972, 2021
132021
Investigation of rs531564 polymorphism in the primary microRNA-124 gene in patients with systemic lupus erythematosus and rheumatoid arthritis: association with disease …
M Hassani, M Dehani, MZ Rafie, E Esmaeilzadeh, S Davar, B Pakzad, ...
Iranian Journal of Allergy, Asthma and Immunology 20 (3), 303-313, 2021
132021
An association study on IL16 gene polymorphisms with the risk of sporadic Alzheimer's disease
T Khoshbakht, M Soosanabadi, M Neishaboury, K Kamali, M Karimlou, ...
Avicenna journal of medical biotechnology 7 (3), 128, 2015
132015
Association study of IL-4-590 C/T and DDX39B-22 G/C polymorphisms with the risk of late-onset alzheimer’s disease in Iranian population
M Soosanabadi, H Bayat, K Kamali, K Saliminejad, M Banan, ...
Current aging science 8 (3), 276-281, 2015
102015
A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome
Z Bahmanpour, Y Daneshmandpour, S Kazeminasab, S Khalil Khalili, ...
International Ophthalmology 41, 389-397, 2021
62021
Dysregulation of long noncoding RNA MEG3 and NLRC5 expressions in patients with relapsing-remitting multiple sclerosis: is there any correlation?
S Torkamandi, S Bahrami, T Ghorashi, M Dehani, H Bayat, SM Hoseini, ...
Genes & Immunity 22 (7), 322-326, 2021
52021
Application of multiplex ligation-dependent probe amplification in determining the copy number alterations of her gene family members in invasive ductal breast carcinoma
M Soosanabadi, R Mirfakhraie, L Atanesyan, A Biglarian, FA Moghadam, ...
Reports of Biochemistry & Molecular Biology 8 (1), 91, 2019
52019
Promoter methylation of matrix metallopeptidase 9 in peripheral blood mononuclear cells: A novel biomarker in a promising source for noninvasive colorectal cancer diagnosis
A Shaygannejad, B Sohrabi, SR Rad, F Yousefisadr, H Darvish, ...
Journal of Cancer Research and Therapeutics, 2023
42023
A functional microRNA binding site variant in IL-23R gene in systemic lupus erythematosus and rheumatoid arthritis: is there any correlation?
S Alesaeidi, SE Dizghandi, G Siri, M Mosallaei, T Kenarangi, T Ghorashi, ...
Molecular Biology Reports 49 (12), 11821-11828, 2022
42022
Analysis of SDC2 gene promoter methylation in whole blood for noninvasive early detection of colorectal cancer
G Siri, S Alesaeidi, SE Dizghandi, B Alani, M Mosallaei, M Soosanabadi
Journal of Cancer Research and Therapeutics 18 (Suppl 2), S354-S358, 2022
32022
Expression of ERBB gene family in females with breast cancer and its correlation with clinicopathological characteristics of the disease
M Soosanabadi, AM Ghahfarokhi, F Pourghazi, N Ehtesham, ...
Molecular Biology Reports 49 (9), 8547-8553, 2022
22022
Association study between BAT1 gene variation and late-onset (sporadic) Alzheimer’s disease in Iranian population
M Soosanabadi Farahani, K Kamali, M Karimlou, M Banan, ...
Journal of Arak University of Medical Sciences 16 (6), 65-71, 2013
12013
A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy
SM Ramshe, S Zardadi, E Alehabib, R Nourinia, J Jamshidi, ...
Journal of Ophthalmic & Vision Research 19 (1), 118, 2024
2024
Demethylation of CDKN2A in systemic lupus erythematosus and rheumatoid arthritis: a blood biomarker for diagnosis and assessment of disease activity
A Gravand, S Alesaeidi, S Khoshbakht, M Saghaei, T Kenarangi, ...
Clinical Rheumatology 42 (12), 3387-3395, 2023
2023
Development of an Expression Vector Engineering Strategy Based on tDNA Insulator Element for the Stable Expression of Vascular Endothelial Growth Factor Receptor-Fc Fusion Protein
A Rahimpour, M Mosallaei, F Pourghazi, SH Tabatabaee, R Hoseinpoor, ...
Monoclonal Antibodies in Immunodiagnosis and Immunotherapy 42 (4), 140-144, 2023
2023
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