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Fatemeh Vahidnezhad
Fatemeh Vahidnezhad
UCSC Silicon Valley Extension, University of California, Santa Cruz
Verified email at ucsc.edu
Title
Cited by
Cited by
Year
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
132022
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
52023
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review
S Biglari, AS Moghaddam, MA Tabatabaiefar, R Sherkat, L Youssefian, ...
Genetics in Medicine 26 (2), 101028, 2024
12024
DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity
A Hozhabrpour, M Mojbafan, F Palizban, S Talebi, M Amani, M Garshasbi, ...
DNA repair 136, 103633, 2024
2024
Whole-transcriptome Sequencing-Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency
L Youssefian, AH Saeidian, Z Saffarian, M Ariamanesh, F Abdollahimajd, ...
JID Innovations, 100278, 2024
2024
P244: DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity
H Vahidnezhad, A Hozhabrpour, L Youssefian, F Vahidnezhad
Genetics in Medicine Open 2, 2024
2024
P756: Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review
L Youssefian, S Biglari, AS Moghaddam, AH Saeidian, F Vahidnezhad, ...
Genetics in Medicine Open 2, 101660, 2024
2024
Abstract# 1411492: Loss-of-Function EGFR Mutation in Bartter Syndrome with Neonatal Epithelial Autoinflammation
P Asadi, R Samii, F Vahidnezhad, J Uitto, H Vahidnezhad
Endocrine Practice 29 (5), S44, 2023
2023
876 Loss-of-function EGFR mutation in bartter syndrome with neonatal epithelial autoinflammation
L Youssefian, A Saeidian, E Kalamati, H Hakonarson, F Vahidnezhad, ...
Journal of Investigative Dermatology 143 (5), S150, 2023
2023
P671: Whole-transcriptome-based skin virome profiling in typical epidermodysplasia verruciformis patients reveals infections with α-, β-and γ-HPVs
H Vahidnezhad, L Youssefian, AH Saeidian, J Uitto, F Vahidnezhad, ...
Genetics in Medicine Open 1 (1), 2023
2023
301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa
H Vahidnezhad, L Youssefian, A Tavasoli, N Harvey, H Mahmoudi, ...
Journal of Investigative Dermatology 142 (12), S232, 2022
2022
Productivity measurement in production of Bovine Albumin 22% in Iranian Blood Research and Fractionation Holding Company (IBRF)
F Vahidnezhad, SM Akrami, AE Jahromi
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