| Klippel–Trenaunay syndrome belongs to the PIK3CA‐related overgrowth spectrum (PROS) H Vahidnezhad, L Youssefian, J Uitto Experimental dermatology 25 (1), 17-19, 2016 | 233 | 2016 |
| The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses SJ De Jong, A Créquer, I Matos, D Hum, V Gunasekharan, L Lorenzo, ... Journal of Experimental Medicine 215 (9), 2289-2310, 2018 | 129 | 2018 |
| Molecular pathology of the basement membrane zone in heritable blistering diseases:: The paradigm of epidermolysis bullosa J Uitto, C Has, H Vahidnezhad, L Youssefian, L Bruckner-Tuderman Matrix Biology 57, 76-85, 2017 | 91 | 2017 |
| Research techniques made simple: whole-transcriptome sequencing by RNA-Seq for diagnosis of monogenic disorders AH Saeidian, L Youssefian, H Vahidnezhad, J Uitto Journal of investigative dermatology 140 (6), 1117-1126. e1, 2020 | 86 | 2020 |
| Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy V Béziat, F Rapaport, J Hu, M Titeux, MB Des Claustres, M Bourgey, ... Cell 184 (14), 3812-3828. e30, 2021 | 77 | 2021 |
| Applications of spherical nucleic acid nanoparticles as delivery systems A Mokhtarzadeh, H Vahidnezhad, L Youssefian, J Mosafer, B Baradaran, ... Trends in molecular medicine 25 (12), 1066-1079, 2019 | 74 | 2019 |
| Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy H Vahidnezhad, L Youssefian, AH Saeidian, H Mahmoudi, A Touati, ... Matrix Biology 66, 22-33, 2018 | 70 | 2018 |
| Genotype–phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis JK Simpson, M Martinez‐Queipo, A Onoufriadis, S Tso, E Glass, L Liu, ... British Journal of Dermatology 182 (3), 729-737, 2020 | 69 | 2020 |
| Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families L Youssefian, H Vahidnezhad, AH Saeidian, A Touati, S Sotoudeh, ... Human mutation 40 (3), 288-298, 2019 | 66 | 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 | 64* | 2019 |
| Dystrophic epidermolysis bullosa: COL7A1 mutation landscape in a multi-ethnic cohort of 152 extended families with high degree of customary consanguineous marriages H Vahidnezhad, L Youssefian, S Zeinali, AH Saeidian, S Sotoudeh, ... Journal of Investigative Dermatology 137 (3), 660-669, 2017 | 61 | 2017 |
| Phenotypic spectrum of epidermolysis bullosa: the paradigm of syndromic versus non-syndromic skin fragility disorders H Vahidnezhad, L Youssefian, AH Saeidian, J Uitto Journal of Investigative Dermatology 139 (3), 522-527, 2019 | 55 | 2019 |
| 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 | 51 | 2019 |
| Kindler syndrome L Youssefian, H Vahidnezhad, J Uitto | 50 | 2022 |
| Molecular genetics of the PI3K-AKT-mTOR pathway in genodermatoses: diagnostic implications and treatment opportunities H Vahidnezhad, L Youssefian, J Uitto Journal of Investigative Dermatology 136 (1), 15-23, 2016 | 49 | 2016 |
| Research techniques made simple: genome-wide homozygosity/autozygosity mapping is a powerful tool for identifying candidate genes in autosomal recessive genetic diseases H Vahidnezhad, L Youssefian, A Jazayeri, J Uitto Journal of Investigative Dermatology 138 (9), 1893-1900, 2018 | 46 | 2018 |
| Multigene next-generation sequencing panel identifies pathogenic variants in patients with unknown subtype of epidermolysis bullosa: subclassification with prognostic implications H Vahidnezhad, L Youssefian, AH Saeidian, A Touati, S Sotoudeh, ... Journal of Investigative Dermatology 137 (12), 2649-2652, 2017 | 44 | 2017 |
| The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families L Youssefian, H Vahidnezhad, M Barzegar, Q Li, S Sotoudeh, ... The Journal of investigative dermatology 135 (5), 1447-1450, 2015 | 44 | 2015 |
| Gene-targeted next generation sequencing identifies PNPLA1 mutations in patients with a phenotypic spectrum of autosomal recessive congenital ichthyosis: the impact of … H Vahidnezhad, L Youssefian, AH Saeidian, S Zeinali, P Mansouri, ... Journal of Investigative Dermatology 137 (3), 678-685, 2017 | 40 | 2017 |
| Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and … H Vahidnezhad, L Youssefian, AH Saeidian, A Touati, S Sotoudeh, ... Human mutation 39 (10), 1349-1354, 2018 | 39 | 2018 |
Hassan VahidnezhadUniversity of Pennsylvania and Children's Hospital of PhiladelphiaZweryfikowany adres z chop.edu