| Effects of cannabinoid receptor type 2 in respiratory syncytial virus infection in human subjects and mice A Tahamtan, Y Samieipoor, FS Nayeri, AA Rahbarimanesh, A Izadi, ... Virulence 9 (1), 217-230, 2018 | 58 | 2018 |
| Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran M Nourizadeh, L Shakerian, S Borte, M Fazlollahi, M Badalzadeh, ... Scandinavian Journal of Immunology 88 (2), e12699, 2018 | 42 | 2018 |
| Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability A Heidari, C Tongsook, R Najafipour, L Musante, M Vasli, M Garshasbi, ... Hum Mol Genet 24 (20), 5697-710, 2015 | 40 | 2015 |
| Transforming growth factor-β1 codon 10 polymorphism is associated with acute GVHD after allogenic BMT in Iranian population MR Noori–Daloii, A Rashidi–Nezhad, P Izadi, A Hossein–Nezhad, ... Annals of transplantation 12 (4), 5-10, 2007 | 29 | 2007 |
| The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile A Rashidi-Nezhad, S Talebi, H Saebnouri, SM Akrami, A Reymond BMC medical genetics 15, 1-6, 2014 | 23 | 2014 |
| CTLA-4 GENE POLYMORPHISMS (-318 C/T,+ 49 A/G,+ 6230 A/G) IN IRANIAN PATIENTS WITH MULTIPLE SCLEROSIS A Heidari, M Keramatipour, AA Amirzargar, A Rashidinezhad, ... IRANIAN JOURNAL OF ALLERGY, ASTHMA AND IMMUNOLOGY (IJAAI) 9 (4), 219-223, 2010 | 17 | 2010 |
| Association of SP-C gene codon 186 polymorphism (rs1124) and risk of RDS N Fatahi, H Dalili, M Kalani, N Niknafs, M Shariat, J Tavakkoly-Bazzaz, ... The Journal of Maternal-Fetal & Neonatal Medicine 30 (21), 2585-2589, 2017 | 14 | 2017 |
| Use of siRNA in knocking down of dopamine receptors, a possible therapeutic option in neuropsychiatric disorders MR Noori-Daloii, M Mojarrad, A Rashidi-Nezhad, M Kheirollahi, ... Molecular biology reports 39, 2003-2010, 2012 | 14 | 2012 |
| Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS N Fatahi, N Niknafs, M Kalani, H Dalili, M Shariat, E Amini, ... The Journal of Maternal-Fetal & Neonatal Medicine 31 (22), 2965-2970, 2018 | 12 | 2018 |
| 2q34-qter duplication and 4q34. 2-qter deletion in a patient with developmental delay A Rashidi-Nezhad, N Parvaneh, F Farzanfar, C Azimi, L Harewood, ... European Journal of Medical Genetics 55 (3), 203-210, 2012 | 11 | 2012 |
| TGF-β codon 25 polymorphism and the risk of graft-versus-host disease after allogenic hematopoietic stem cell transplantation A Rashidi–Nezhad, C Azimi, K Alimoghaddam, A Ghavamzadeh, ... Iranian Journal of Allergy, Asthma and Immunology, 1-6, 2010 | 11 | 2010 |
| A novel case report of spinal muscular atrophy with progressive myoclonic epilepsy from Iran R Shervin Badv, Y Nilipour, S Rahimi-Dehgolan, A Rashidi-Nezhad, ... International Medical Case Reports Journal, 155-159, 2019 | 10 | 2019 |
| 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 |
| Knocking down the DRD2 by shRNA expressing plasmids in the nucleus accumbens prevented the disrupting effect of apomorphine on prepulse inhibition in rat MR Noori-Daloii, A Shahbazi, S Alizadeh Zendehrood, A Shayan Nia, ... Journal of Sciences, Islamic Republic of Iran 26 (3), 205-212, 2015 | 9 | 2015 |
| Exploring the genetic etiology of drug-resistant epilepsy: incorporation of exome sequencing into practice M Mahdiannasser, A Rashidi-Nezhad, RS Badv, SM Akrami Acta Neurologica Belgica 122 (6), 1457-1468, 2022 | 7 | 2022 |
| Effects of cannabinoid receptor type 2 in respiratory syncytial virus infection in human subjects and mice. Virulence A Tahamtan, Y Samieipoor, FS Nayeri, AA Rahbarimanesh, A Izadi, ... | 5 | 2017 |
| Utilization of whole exome sequencing in lethal form of multiple pterygium syndrome: identification of mutations in embryonal subunit of acetylcholine receptor T Nazari, A Rashidi-Nezhad, M Ganji, Z Rezaei, S Talebi, N Ghasemi, ... International Journal of Molecular and Cellular Medicine 8 (4), 258, 2019 | 4 | 2019 |
| CEP104 gene may involve in the pathogenesis of a new developmental disorder other than joubert syndrome RS Badv, M Mahdiannasser, M Rasoulinezhad, L Habibi, ... Molecular Biology Reports 49 (8), 7231-7237, 2022 | 3 | 2022 |
| Evaluating the pre-, peri-and post-natal conditions of neonates affected by multiple congenital anomalies: a brief report. A Rashidi-Nezhad, L Fakhri, S Hantoush Zadeh, E Amini, N Sajjadian, ... Tehran University Medical Journal 70 (10), 2013 | 2 | 2013 |
| Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies P Vaseghi, L Habibi, JA Neidich, Y Cao, N Fattahi, R Rashidi-Nezhad, ... European Journal of Human Genetics, 1-12, 2024 | 1 | 2024 |
hosein daliliTehran University of Medical SciencesVerified email at tums.ac.ir
