| Molecular and biochemical mechanisms of human iris color: A comprehensive review S Dorgaleleh, K Naghipoor 4th International Congress on Biomedicine, 2020 | 23 | 2020 |
| Recalcitrant cutaneous warts in a family with inherited ICOS deficiency L Youssefian, AH Saeidian, AR Tavasoli, E Kalamati, K Naghipoor, ... Journal of Investigative Dermatology 142 (9), 2435-2445, 2022 | 8 | 2022 |
| Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections AH Saeidian, L Youssefian, M Naji, H Mahmoudi, SM Barnada, C Huang, ... JCI insight 8 (5), 2023 | 5 | 2023 |
| Molecular insight of dyskeratosis congenita: Defects in telomere length homeostasis S Dorgaleleh, K Naghipoor, Z Hajimohammadi, F Dastaviz, M Oladnabi Journal of Clinical and Translational Research 8 (1), 20, 2022 | 4 | 2022 |
| 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 |
| Molecular basis of ectodermal dysplasia: a comprehensive review of the literature S Dorgaleleh, K Naghipoor, Z Hajimohammadi, M Oladnab Egyptian Journal of Dermatology and Venerology 41 (2), 55-66, 2021 | 3 | 2021 |
| Transfusion related adverse effects on beta-thalassemia major and new therapeutic approaches: A review study S Dorgaleleh, A Barahouie, K Naghipoor, F Dastaviz, Z Ghodsalavi, ... International Journal of Pediatrics 8 (7), 11651-11661, 2020 | 3 | 2020 |
| 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 | 2 | 2023 |
| Ectodermal Dysplasia patients susceptible to COVID-19 S Dorgaleleh, K Naghipoor, M Oladnabi Health Biotechnology and Biopharma (HBB) 6 (2), 78-80, 2022 | 2 | 2022 |
| The role of different genes in causing infection of ectodermal dysplasia patients: A systematic review S Dorgaleleh, Z Toutounchi, M Soltani, K Naghipoor, M Oladnabi Health Biotechnology and Biopharma (HBB) 5 (4), 86-104, 2022 | 2 | 2022 |
| Telomere shortening occurs in patients with ectodermal dysplasia S Dorgaleleh, K Naghipoor, M Oladnabi Health Biotechnology and Biopharma 4 (4), 1-5, 2021 | 2 | 2021 |
| Detection of the Duplication in Exons 56-63 of Duchenne Muscular Dystrophy Patients with MLPA S Dorgaleleh, K Naghipoor, A Ahmad Barahouie, M Oladnabi International Journal of Pediatrics 8 (7), 11617-11623, 2020 | 2 | 2020 |
| Advances in Treatments for Epidermolysis Bullosa (EB): Emphasis on Stem Cell-Based Therapy R Raoufinia, N Keyhanvar, M Moghbeli, N Abdyazdani, M Rostami, ... Stem Cell Reviews and Reports, 1-13, 2024 | | 2024 |
| Are Dyskeratosis Congenita patients at higher risk of symptomatic COVID-19? S Dorgaleleh, K Naghipoor, A Hozhabrpour, H Vahidnezhad Medical Hypotheses 163, 110843, 2022 | | 2022 |
Saeed DorgalelehPh.D. Student In Medical Genetics,University of Social Welfare and Rehabilitation Sciences, TehranVerified email at goums.ac.ir
