Azadeh Shojaei
Azadeh Shojaei
Department of medical genetics and biology,school of medicine,iran university of medical science
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The effects of omega-3 and vitamin E co-supplementation on parameters of mental health and gene expression related to insulin and inflammation in subjects with polycystic ovary …
M Jamilian, A Shojaei, M Samimi, FA Ebrahimi, E Aghadavod, M Karamali, ...
Journal of affective disorders 229, 41-47, 2018
Coinhibition of overexpressed genes in acute myeloid leukemia subtype M2 by gold nanoparticles functionalized with five antisense oligonucleotides and one anti-CD33 (+)/CD34 (+ …
MA Zaimy, A Jebali, B Bazrafshan, S Mehrtashfar, S Shabani, A Tavakoli, ...
Cancer Gene Therapy 23 (9), 315-320, 2016
Association between tobacco smoking and opioid use: a meta-analysis
A Rajabi, M Dehghani, A Shojaei, M Farjam, SA Motevalian
Addictive behaviors 92, 225-235, 2019
Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss
MA Dowlati, P Derakhshandeh-peykar, M Houshmand, M Farhadi, ...
Molecular biology reports 40 (3), 2689-2695, 2013
Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings
A Shojaei, F Behjati, P Derakhshandeh-Peykar, M Razzaghy-Azar, ...
Gene 517 (1), 137-145, 2013
Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization
F Behjati, SG Firouzabadi, R Kariminejad, R Vameghi, F Sajedi, ...
Indian journal of human genetics 19 (4), 443, 2013
Genetic screening of iranian patients with 46, XY disorders of sex development
A Shojaei, R Ebrahimzadeh-Vesal, A Ahani, M Razzaghy-Azar
Reports of biochemistry & molecular biology 6 (1), 59, 2017
Novel human mitochondrial tRNAphe mutation in a patient with hearing impairment: A case study
MA Dowlati, P Derakhshandeh-Peykar, M Houshmand, M Farhadi, ...
Mitochondrial DNA 24 (2), 132-136, 2013
Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria
MR Moghadam, A Shojaei, V Babaei, F Rohani, F Ghazi
Medical journal of the Islamic Republic of Iran 32, 21, 2018
Mutation analysis of androgen receptor gene: multiple uses for a single test
A Shojaei, F Behjati, R Ebrahimzadeh-Vesal, M Razzaghy-Azar, ...
Gene 552 (2), 234-238, 2014
Complex Alleles of CYP21A2 Are the Most Frequent Causes of Congenital Adrenal Hyperplasia in Iranian Population
NA Kollahi, F Rohani, F Baghbani-arani, A Shojaei
Iranian Journal of Pediatrics 29 (6), 2019
The association between polymorphism of the BDNF gene and cigarette smoking in the Iranian population
A Rajabi, P Khosravi, SA Motevalian, M Farjam, A Shojaei
The journal of gene medicine 20 (10-11), e3052, 2018
Association of homeobox B13 (HOXB13) gene variants with prostate cancer risk in an Iranian population
R Roudi, H Nemati, MR Moghadam, M Sotoudeh, B Narouie, A Shojaei
Medical Journal of the Islamic Republic of Iran 32, 97, 2018
Molecular genetic analysis of Steroid Resistant Nephrotic Syndrome: Detection of a novel mutation
N Serajpour, B Karimi, N Hooman, R Hosseini, P Khosravi, HM Rasouly, ...
bioRxiv, 305987, 2018
The Occurrence of potential and novel isolates of Oceanobacillus sp. JAS12 and Salinicoccus sp. JS20 recovered from West Coast of Arabian Sea, India
YA Jayachandra, MB Sulochana, KH Merja, AB Parameshwar, ...
Research journal of biotechnology, 2020
Complex Alleles of CYP21A2 Are the Most Frequent Causes of Congenital Adrenal Hyperplasia in Iranian Population
N Asghari Kollahi, F Rohani, F Baghbani-arani, A Shojaei
Iranian Journal of Pediatrics 29 (6), 2019
Evaluation of gene expression level of GPRC6A, E. cadherin and ZEB1 in prostate cancer in comparison to benign tissues
R Ghasemi, A Shojaei, B Karimi
Tehran University Medical Journal TUMS Publications 77 (2), 69-75, 2019
بررسی فراوانی جهش cluster E6 در ژن CYP21A2 در بیماران مبتلا به هایپرپلازی مادرزادی آدرنال در جمعیت ایرانی
باغبانی, شجاعی, آزاده, اصغری, ندا
Research in Medicine 42 (2), 116-120, 2018
Disorders of sex developement: involved genes and genetic counseling
R Jafaryazdi, A Shojaei
Razi Journal of Medical Sciences 25 (167), 30-48, 2018
Investigation of exon 6 cluster mutation in CYP21A2 gene in Iranian patients with congenital adrenal hyperplasia
PAJOUHESH DAR PEZESHKI 42 (200204), 116-120, 2018
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