| The role of miRNAs and lncRNAs in neurofibromatosis type 1 T Khosravi, M Oladnabi Journal of Cellular Biochemistry 124 (1), 17-30, 2023 | 6 | 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 | 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 | 3 | 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 |
| To what extent does ChatGPT understand genetics? T Khosravi, ZM Al Sudani, M Oladnabi Innovations in Education and Teaching International, 1-10, 2023 | 2 | 2023 |
| 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 |
| 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 | | 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 |
| 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 |
| 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, GorganVerified email at goums.ac.ir
