| A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract M Behnam, E Imagawa, ARS Chaleshtori, F Ronasian, M Salehi, ... Journal of human genetics 61 (2), 177-179, 2016 | 25 | 2016 |
| A novel 8-bp duplication in ADAT3 causes mild intellectual disability AR Salehi Chaleshtori, N Miyake, M Ahmadvand, O Bashti, N Matsumoto, ... Human Genome Variation 5 (1), 7, 2018 | 24 | 2018 |
| Detection of SEA, SEB, SEC, SEQ genes in Staphylococcus aureus isolated from nasal carriers in tehran province, Iran, by MULTIPLEX PCR M Saadati, B Barati, M Doroudian, H Shirzad, M Hashemi, SM Hosseini, ... ARCHIVES OF ADVANCES IN BIOSCIENCES (JOURNAL OF PARAMEDICAL SCIENCES) 2 (2 …, 2011 | 24 | 2011 |
| Novel missense variants in ADAT3 as a cause of syndromic intellectual disability E Thomas, AM Lewis, Y Yang, S Chanprasert, L Potocki, DA Scott Journal of Pediatric Genetics 8 (04), 244-251, 2019 | 18 | 2019 |
| Assessment of the effects of IL9, IL9R, IL17A, and IL17F gene polymorphisms on women with allergic rhinitis in Shahrekord, Iran F Fatahi, ARS Chaleshtori, KG Samani, SM Mousavi, F Zandi, S Heydari, ... Annals of medical and health sciences research 6 (4), 216-223, 2016 | 10 | 2016 |
| Another novel missense mutation in ARSB gene in Iran S Abbasi, M Noruzinia, O Bashti, M Ahmadvand, ARS Chaleshtori, ... Acta Medica Iranica, 585-590, 2017 | 8 | 2017 |
| Study of Antimetastatic Effect of Genistein Through Inhibition of Expression of Matrix Metalloproteinase in A-549 Cell Line AG M.R. Noori-Daloii, M. Saffari, O. Saydi Dinekabodi, B. Rahmani, A.R ... Journal of Sciences, Islamic Republic of Iran 23 (2), 115-122, 2012 | 8 | 2012 |
| Kleefstra syndrome: the first case report from Iran M Noruzinia, M Ahmadvand, O Bashti, ARS Chaleshtori Acta Medica Iranica, 650-654, 2017 | 7 | 2017 |
| Application of Epstein–Barr virus for optimization of immortalized B-lymphocyte production as a positive control in genetic studies B Tousizadeh, S Moghim, ARS Chaleshtori, M Ghanbarian, M Mirian, ... Advanced biomedical research 6 (1), 80, 2017 | 5 | 2017 |
| The identification of two pathogenic variants in a family with mild and severe forms of developmental delay N Miyake, S Heydari, M Garshasbi, S Saitoh, J Nasiri, K Hamanaka, ... Journal of Human Genetics 66 (4), 445-448, 2021 | 3 | 2021 |
| The identification and stereochemistry analysis of a novel mutation p.(D367Tfs* 61) in the CYP1B1 gene: A case report ARS Chaleshtori, M Garshasbi, A Salehi, M Noruzinia Journal of current ophthalmology 32 (1), 114-118, 2020 | 3 | 2020 |
| A novel deletion mutation in GUCY2D gene may be responsible for Leber congenital amaurosis-1 disease: A case report ARS Chaleshtori, M Garshasbi, A Salehi Journal of Current Ophthalmology 31 (4), 458-462, 2019 | 2 | 2019 |
| Evaluation of live attenuated Shigella dysenteriae type 1 strain as a candidate vaccine AR Salehi Chaleshtori, M Saadati, Y Ahsani Arani, A Bahador, M Hosseini, ... Journal of Police Medicine 1 (1), 31-39, 2012 | 2 | 2012 |
| λ-Red-recombineering live Attenuated ΔipaD Shigella dysenteriae from iranian isolates as a candidate of vaccine A Salehi, M Saadati, R Raoofian, A Bahador, M Doroudian, Y Ahsanim, ... Journal of Sciences, Islamic Republic of Iran 23 (1), 21-28, 2012 | 2 | 2012 |
| Genetic linkage analysis of DFNB93 locus in a group of families with autosomal recessive non-syndromic hearing loss in Chahar Mahal & Bakhtiari and Kohkiluyeh & Boyer Ahmad … F Rezaeian, MA Tabatabaiefar, F Heybati, S Reiisi, S Parchami, ... Journal of Shahrekord University of Medical Sciences 16 (4), 62-70, 2014 | 1 | 2014 |
| Generation mutant construct of pgem-7zf:: ΔIcsa (catr) for attenuation of Shigella flexneri 2A M Doroudian, M Saadati, A Ghahroudi, D Jahantigh, AR Salehi, ... IRANIAN JOURNAL OF INFECTIOUS DISEASES AND TROPICAL MEDICINE 17 (59), 41-47, 2013 | 1 | 2013 |
| Evaluation of Antibiotic Resistance to Fluoroquinolones and Third Generation Cephalosporines in Iranian Clinical Isolates of Salmonella spp. N Sepehri Rad, MR Razavi, SD Siadat, MR Aghasadeghi, B Rajaei, ... International Journal of Molecular and Clinical Microbiology 2 (2), 194-198, 2012 | 1 | 2012 |
| Possible dual contribution of a novel GUCY2D mutation in the development of retinal degeneration in a consanguineous population ARS Chaleshtori, M Garshasbi, A Salehi, M Noruzinia European Journal of Medical Genetics 63 (3), 103750, 2020 | | 2020 |
| A Splicing Variant in OCRL Gene Might Explain the Second Case of Lowe Syndrome in Iran M Houshmand, G Babamohammadi, H Moazzeni, ARS Chaleshtori, ... Journal of Human Genetics and Genomics 3 (1), 2019 | | 2019 |
| Novel Single Base Pair Deletion in ATM Cause Ataxia Telangiectasia in an Iranian Proband M Ahmadvand, O Bashti, ARS Chaleshtori, M Noruzinia Archives of Advances in Biosciences 8 (3), 59-64, 2017 | | 2017 |
Mehrdad NoruziniaAssociate professor, Department of Medical Genetics, Faculty of Medicine, Tarbiat Modares Universitymodares.ac.ir üzerinde doğrulanmış e-posta adresine sahip
