Whole-transcriptome sequencing–based concomitant detection of viral and human genetic determinants of cutaneous lesions AH Saeidian, L Youssefian, CY Huang, F Palizban, M Naji, Z Saffarian, ... JCI insight 7 (8), 2022 | 15 | 2022 |
Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation H Vahidnezhad, L Youssefian, AH Saeidian, LM Boyden, A Touati, ... Matrix Biology 99, 43-57, 2021 | 9 | 2021 |
Keratitis‐ichthyosis‐deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation T Asgari, M Naji, P Mansouri, H Mahmoudi, M Zabihi, L Youssefian, ... Dermatologic Therapy 33 (6), e14493, 2020 | 9 | 2020 |
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 | 7 | 2023 |
Chapter 1: role of digital health, mhealth, and low-cost technologies in advancing universal health coverage in emerging economies P Murthy, M Naji Technology and Global Public Health, 31-46, 2020 | 5 | 2020 |
Ichthyosis follicularis syndromes in patients with mutations in GJB2 L Youssefian, M Naji, JS Park, F Rajabi, F Abdollahimajd, H Mahmoudi, ... Clinical and Experimental Dermatology 47 (8), 1561-1566, 2022 | 1 | 2022 |
185 GJB2 mutations in patients with ichthyosis follicularis and histopathology of porokeratotic adnexal ostial nevus L Youssefian, F Abdollahimajd, M Naji, F Rajabi, H Mahmoudi, KK Hesari, ... Journal of Investigative Dermatology 141 (5), S33, 2021 | | 2021 |