Leila Youssefian
Thomas Jefferson University
H-index: 25
North America-United States
Top articles of Leila Youssefian
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity | DNA repair | Amir Hozhabrpour Marzieh Mojbafan Fahimeh Palizban Saeed Talebi Maliheh Amani | 2024/4/1 |
Whole-transcriptome Sequencing-Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency | JID Innovations | Leila Youssefian Amir Hossein Saeidian Zahra Saffarian Mona Ariamanesh Fahimeh Abdollahimajd | 2024/3/27 |
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review | Sajjad Biglari Atefeh Sohanforooshan Moghaddam Mohammad Amin Tabatabaiefar Roya Sherkat Leila Youssefian | 2024/2/1 | |
P244: DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity | Genetics in Medicine Open | Hassan Vahidnezhad Amir Hozhabrpour Leila Youssefian Fatemeh Vahidnezhad | 2024/1/1 |
P756: Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review | Leila Youssefian Sajjad Biglari Atefeh Sohanforooshan Moghaddam Amir Hossein Saeidian Fatemeh Vahidnezhad | 2024/1/1 | |
Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug‐induced associations | Jason S Park Amir H Saeidian Leila Youssefian Sylvia Hsu Hassan Vahidnezhad | 2023/1 | |
Interpretation of genomic sequence variants in heritable skin diseases: A primer for clinicians | Jouni Uitto Amir Hossein Saeidian Leila Youssefian Hassan Vahidnezhad | 2023/9/1 | |
876 Loss-of-function EGFR mutation in bartter syndrome with neonatal epithelial autoinflammation | Journal of Investigative Dermatology | L Youssefian A Saeidian E Kalamati H Hakonarson F Vahidnezhad | 2023/5/1 |
Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections | JCI insight | Amir Hossein Saeidian Leila Youssefian Mahtab Naji Hamidreza Mahmoudi Samantha M Barnada | 2023/3/3 |
P671: Whole-transcriptome-based skin virome profiling in typical epidermodysplasia verruciformis patients reveals infections with α-, β-and γ-HPVs | Genetics in Medicine Open | Hassan Vahidnezhad Leila Youssefian Amir Hossein Saeidian Jouni Uitto Fatemeh Vahidnezhad | 2023/1/1 |
P366: Loss-of-function EGFR mutation in Bartter syndrome with neonatal epithelial autoinflammation | Genetics in Medicine Open | Leila Youssefian Hassan Vahidnezhad Jouni Uitto Amir Hossein Saeidian Rana Samii | 2023/1/1 |
Whole‐transcriptome sequencing identifies postzygotic ATP2A2 mutations in a patient misdiagnosed with herpes zoster, confirming the diagnosis of very late‐onset … | Experimental Dermatology | Fatemeh Mohaghegh Leila Youssefian Hamid Galehdari Narjes Tavakoli Hassan Vahidnezhad | 2022/6 |
495 Mutations in different domains of bullous pemphigoid antigen-1 (BPGA1) encoded by DST result in either epidermolysis bullosa simplex or musculoskeletal and neuronal … | Journal of Investigative Dermatology | N Harvey R Khalesi M Garshasbi E Kalamati L Youssefian | 2022/8/1 |
Mutation update: The spectra of PLEC sequence variants and related plectinopathies | Human mutation | Hassan Vahidnezhad Leila Youssefian Nailah Harvey Ali Reza Tavasoli Amir Hossein Saeidian | 2022/12 |
Ichthyosis follicularis syndromes in patients with mutations in GJB2 | Clinical and Experimental Dermatology | Leila Youssefian Mahtab Naji Jason S Park Fateme Rajabi Fahimeh Abdollahimajd | 2022/8/1 |
Epidermolysis bullosa and the COVID-19 pandemic: challenges and recommendations | Journal of Dermatological Treatment | Hassan Vahidnezhad Hamideh Moravvej Ayda Bahmanjahromi Leila Youssefian Fahimeh Abdollahimajd | 2022/2/17 |
Novel splice mutation in CDSN gene causing type b peeling skin syndrome. | Journal of the European Academy of Dermatology and Venereology: JEADV | I Navarro-Navarro D Jiménez-Gallo R de la Varga-Martínez I Villegas-Romero F Mora-López | 2022/6 |
309 Losartan treatment improves recessive dystrophic Epidermolysis bullosa | Journal of Investigative Dermatology | M Pourani H Vahidnezhad L Youssefian A Rakhshan B Hajimoradi | 2022/8/1 |
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis | Journal of Experimental Medicine | Masato Ogishi Rui Yang Rémy Rodriguez Dominic P Golec Emmanuel Martin | 2022/11/3 |
Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case series | Dermatologic Therapy | Mohammad Reza Pourani Hassan Vahidnezhad Parvin Mansouri Leila Youssefian Azadeh Rakhshan | 2022/7 |
Co-Authors
