| The role of miRNAs and lncRNAs in neurofibromatosis type 1 T Khosravi, M Oladnabi Journal of Cellular Biochemistry 124 (1), 17-30, 2023 | 8 | 2023 |
| Frequency of c.35delG Mutation in GJB2 Gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran M Hajilari, A Sharifinya, T Khosravi, A Kianmehr, MH Taziki, A Khosravi, ... International Journal of Pediatrics, 2023 | 5 | 2023 |
| To what extent does ChatGPT understand genetics? T Khosravi, ZM Al Sudani, M Oladnabi Innovations in Education and Teaching International, 1-10, 2023 | 4 | 2023 |
| Whole exome sequencing identifies a novel variant in the COL12A1 gene in a family with Ullrich congenital muscular dystrophy 2 K Naghipoor, T Khosravi, M Oladnabi Molecular Biology Reports 50 (9), 7427-7435, 2023 | 4 | 2023 |
| Whole Exome Sequencing Reveals the First c.7456C>T p.Arg2486X Mutation in ATM Gene in Iranian Population S Dorgaleleh, K Naghipoor, T Khosravi, A Tadayoni Nia, ... Health Biotechnology and Biopharma (HBB) 6 (3), 57-72, 2022 | 3 | 2022 |
| A novel biallelic 19-bp deletion in the IL10RB gene caused infant-onset inflammatory bowel disease in a consanguineous family: a molecular docking simulation study and … F Motallebi, ZM Al Sudani, F Vaghefi, T Khosravi, A Rahimzadeh, ... Molecular Biology Reports 51 (1), 223, 2024 | 1 | 2024 |
| Hearing loss among families with 2 and more affected members in golestan province, Iran: a cross-sectional study of 320 families ZM Al Sudani, T Khosravi, M Oladnabi The Journal of International Advanced Otology 20 (1), 44, 2024 | 1 | 2024 |
| Impact of umbelliprenin-containing niosome nanoparticles on VEGF-A and CTGF genes expression in retinal pigment epithelium cells F Dastaviz, A Vahidi, T Khosravi, A Khosravi, MS Arabi, A Bagheri, ... International Journal of Ophthalmology 17 (1), 7, 2024 | 1 | 2024 |
| Second report of TEDC1-related microcephaly caused by a novel biallelic mutation in an Iranian consanguineous family A Sarli, ZM Al Sudani, F Vaghefi, F Motallebi, T Khosravi, N Rezaie, ... Molecular Biology Reports 51 (1), 181, 2024 | | 2024 |
| A Rare Combination of Compound Heterozygous Mutations in the PAH Gene in Three Unrelated Consanguineous Iranian Families with Classical Phenylketonuria A Rahimzadeh, T Khosravi, F Motallebi, ZM Al Sudani, F Vaghefi, ... Advanced Biomedical Research 13, 64, 2024 | | 2024 |
| In silico analysis of mutation spectrum of Ehlers–Danlos, osteogenesis imperfecta, and cutis laxa overlapping phenotypes in Iranian population T Khosravi, K Naghipoor, F Vaghefi, AM Falahati, M Oladnabi Egyptian Journal of Medical Human Genetics 25 (1), 8, 2024 | | 2024 |
| A comprehensive in silico analysis of mutation spectrum of maple syrup urine disease (MSUD) genes in Iranian population N Rezaie, SS Ghazanfari, T Khosravi, F Vaghefi, M Oladnabi Molecular Biology Research Communications 13 (4), 235, 2024 | | 2024 |
| Niosome-encapsulated auraptene reduced the mRNA expression of VEGF-A and PDGFs genes in human retina-derived RPE cell line A Vahidi, T Khosravi, F Dastaviz, MS Arabi, A Khosravi, M Oladnabi International Journal of Ophthalmology 17 (6), 1028, 2024 | | 2024 |
| An overview of miRNAs role in neurofibromatosis type 2 N Rezaie, T Khosravi, A Vahidi, M Oladnabi Health Biotechnology and Biopharma (HBB) 7 (2), 1-17, 2023 | | 2023 |
Morteza oladnabiGorgan Congenital Malformations Research Center, Golestan University of Medical Sciences, Gorgan在 goums.ac.ir 的电子邮件经过验证
Morteza oladnabiGorgan Congenital Malformations Research Center, Golestan University of Medical Sciences, Gorgan在 goums.ac.ir 的电子邮件经过验证
Zainab M. Al-sudaniMedical student , Golestan university of Medical Sciences在 goums.ac.ir 的电子邮件经过验证