| 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 | 63 | 2019 |
| 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 | 61 | 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 | 23 | 2016 |
| 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 | 19 | 2018 |
| 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, 2689-2695, 2013 | 16 | 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 | 10 | 2013 |
| Genetic screening of iranian patients with 46, XY disorders of sex development A Shojaei, R Ebrahimzadeh-Vesal, A Ahani, M Razzaghy-Azar, F Ghazi, ... Reports of biochemistry & molecular biology 6 (1), 59, 2017 | 9 | 2017 |
| Cigarette smoking behavior a gateway to opium use disorder: a Mendelian randomization analysis A Rajabi, A Shojaei, L Janani, M Farjam, HR Baradaran, P Khosravi, ... Behavior Genetics 51, 385-393, 2021 | 7 | 2021 |
| 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 | 6 | 2018 |
| A homozygous loss-of-function mutation in PTPN14 causes a syndrome of bilateral choanal atresia and early infantile-onset lymphedema: PTPN14 mutation in lymphedema-choanal atresia A Bordbar, R Maroofian, P Ostergaard, M Kashaki, S Nikpour, K Gordon, ... Meta Gene 14, 53-58, 2017 | 6 | 2017 |
| 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 | 6 | 2013 |
| 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 | 6 | 2013 |
| High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases M Najafi, KM Riedhammer, A Rad, PN Torbati, R Berutti, I Schüle, ... Frontiers in Pediatrics 10, 974840, 2022 | 4 | 2022 |
| 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 | 4 | 2019 |
| 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 | 4 | 2018 |
| 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 | 3 | 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 | 3 | 2014 |
| New report of a different clinical presentation of CD151 splicing mutation (c. 351+ 2T> C): Could TSPAN11 be considered as a potential modifier gene for CD151? N Rahmani, S Talebi, R Hoseini, N Asghari Kollahi, A Shojaei Molecular Syndromology 13 (3), 212-220, 2022 | 2 | 2022 |
| Investigation of RBC Indices and HbA2 Levels in Parents of Beta-Thalassemia Patients: Impacts on Premarital Genetic Counseling M Izadyar, J Dastan, T Sabokbar, S Shoraka, A Shojaei, H Nasiri, ... Journal of family and reproductive health, 89-91, 2007 | 2 | 2007 |
| Disorders of sex development: involved genes and genetic counseling R Jafaryazdi, A Shojaei RAZI JOURNAL OF MEDICAL SCIENCES (JOURNAL OF IRAN UNIVERSITY OF MEDICAL …, 2018 | 1 | 2018 |
