| Antipsychotic drugs attenuate aberrant DNA methylation of DTNBP1 (dysbindin) promoter in saliva and post‐mortem brain of patients with schizophrenia and … HM Abdolmaleky, S Pajouhanfar, M Faghankhani, MT Joghataei, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 …, 2015 | 71 | 2015 |
| Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations L Youssefian, H Vahidnezhad, AH Saeidian, S Pajouhanfar, S Sotoudeh, ... Journal of hepatology 71 (2), 366-370, 2019 | 48 | 2019 |
| Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with … H Vahidnezhad, L Youssefian, AH Saeidian, A Touati, S Pajouhanfar, ... Matrix Biology 81, 91-106, 2019 | 48 | 2019 |
| Factors affecting smartphone adoption for accessing information in medical settings I Tahamtan, S Pajouhanfar, S Sedghi, M Azad, M Roudbari Health Information & Libraries Journal 34 (2), 134-145, 2017 | 31 | 2017 |
| The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series L Youssefian, H Vahidnezhad, A Touati, V Ziaee, AH Saeidian, ... BMC Medical Genetics 19, 1-5, 2018 | 13 | 2018 |
| Mutations in PLOD3, encoding lysyl hydroxylase 3, cause syndromic recessive dystrophic epidermolyis bullosa-like phenotype with abnormal anchoring fibrils and deficiency in … H Vahidnezhad, L Youssefian, AH Saeidian, A Touati, S Pajouhanfar, ... Matrix Biol 81, 91-106, 2019 | 10 | 2019 |
| Transition to psychosis: Evaluation of the first-degree relatives of patients with schizophrenia M Hormozpour, H Amini, S Pajouhanfar, M Faghankhani, A Rahmani, ... Iranian journal of psychiatry 11 (1), 15, 2016 | 10 | 2016 |
| The matriptase‐prostasin proteolytic cascade in dermatologic diseases A Touati, AH Saeidian, L Youssefian, M Faghankhani, F Niaziorimi, ... Experimental Dermatology 29 (7), 580-587, 2020 | 8 | 2020 |
| Principles and applications of CRISPR toolkit in virus manipulation, diagnosis, and virus-host interactions S Jamehdor, S Pajouhanfar, S Saba, G Uzan, A Teimoori, S Naserian Cells 11 (6), 999, 2022 | 4 | 2022 |
| Novel PTCH1 and concurrent TP53 mutations in four patients with numerous non‐syndromic basal cell carcinomas: The paradigm of oncogenic synergy B Dasgeb, S Pajouhanfar, A Jazayeri, E Schoenberg, G Kumar, P Fortina, ... Experimental Dermatology 31 (5), 736-742, 2022 | 3 | 2022 |
| The effects of quercetin on the gene expression of arginine metabolism key enzymes in human embryonic kidney 293 cells S Jamehdor, S Farivar, MH Sangtarash, R Amini, S Pajouhanfar, ... Jundishapur Journal of Natural Pharmaceutical Products 16 (2), 2021 | 2 | 2021 |
| The role of miRNA134 in pathogenesis and treatment of intractable epilepsy: a review article M Kasaiyan, M Basiri, S Pajouhanfar Nucleosides, Nucleotides & Nucleic Acids, 1-16, 2024 | | 2024 |
| Inherited Nonalcoholic Fatty Liver Disease and/or Dyslipidemia Due to Monoallelic ABHD5 Mutations S Pajouhanfar, S Sotoudeh, MD Roberto Colombo, MD Jouni Uitto The American Journal of Gastroenterology 113, S507-S510, 2018 | | 2018 |
| Identification of Differentially Expressed Proteins in Mice Models of Down Syndrome Using Bipartite Networks S Pajouhanfar, S Geiler, A Amirhamzeh, S Saba, M Kasaiyan, A Jazayeri, ... 2019 Mid-Atlantic Bioinformatics Conference, 0 | | |
