Hassan Vahidnezhad
Thomas Jefferson University
H-index: 25
North America-United States
Top articles of Hassan Vahidnezhad
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
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 |
RARS1‐related hypomyelinating leukodystrophy‐9 (HLD‐9) in two distinct Iranian families: Case report and literature review | Sajjad Biglari Hassan Vahidnezhad Mohammad Amin Tabatabaiefar Hamid Reza Khorram Khorshid Emran Esmaeilzadeh | 2024/4 | |
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 | |
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 |
Correlation between Melphalan chemotherapy with longitudinal global strain indices of the left ventricle in multiple myeloma patients: a velocity vector imaging (VVI … | Caspian Journal of Internal Medicine | Liaosadat Mirsafaee Mohammad Dehghani Firouzabadi Sayeh Parkhideh Hassan Vahidnezhad Fatemeh Dehghani Firouzabadi | 2024 |
A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies | Brain and Development | Sareh Hosseinpour Ehsan Razmara Morteza Heidari Zahra Rezaei Mahmoud Reza Ashrafi | 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 | |
Abstract# 1411492: Loss-of-Function EGFR Mutation in Bartter Syndrome with Neonatal Epithelial Autoinflammation | Endocrine Practice | Poupak Asadi Rana Samii Fatemeh Vahidnezhad Jouni Uitto Hassan Vahidnezhad | 2023/5/1 |
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 | |
640 Treatment of recalcitrant cutaneous warts with intralesional injection of HBV vaccine | Journal of Investigative Dermatology | N Najar Nobari H Keyvani A Goodarzi H Keramati M Najar Nobari | 2023/5/1 |
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 |
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry | neurogenetics | Mahmoudreza Ashrafi Reyhaneh Kameli Sareh Hosseinpour Ehsan Razmara Zahra Zamani | 2023/10 |
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 |
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients | Orphanet journal of rare diseases | Ali Zare Dehnavi Maryam Bemanalizadeh Seyyed Mohammad Kahani Mahmoud Reza Ashrafi Mohammad Rohani | 2023/7/5 |
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 |
Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP | L Youssefian S Khodavaisy F Khosravi‐Bachehmir JS Park AH Saeidian | 2022/3 | |
Pathomechanisms of epidermolysis bullosa: Beyond structural proteins | Nailah Harvey Leila Youssefian Amir Hossein Saeidian Hassan Vahidnezhad Jouni Uitto | 2022/6/1 | |
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 |
Co-Authors
