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Human Mutation|July 11, 2022
Mutation update: The spectra of PLEC sequence variants and related plectinopathiesHassan Vahidnezhad, Leila Youssefian, Nailah Harvey, et al.
The Journal of Investigative Dermatology|November 26, 2016
Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of ConsanguinityHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
JAMA Dermatology|October 13, 2021
Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of InheritanceHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Human Mutation|November 16, 2018
A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratodermaLeila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, et al.
Human Mutation|July 18, 2018
Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosaHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.
Clinical Epigenetics|October 11, 2025
DNA methylation and machine learning: challenges and perspective toward enhanced clinical diagnosticsErfan Aref-Eshghi, Arash B Abadi, Mohammad-Erfan Farhadieh, et al.
Clinical and Experimental Dermatology|April 9, 2022
Ichthyosis follicularis syndromes in patients with mutations in GJB2Leila Youssefian, Mahtab Naji, Jason S Park, et al.
Experimental Dermatology|April 17, 2020
Linear basal cell nevus with a novel mosaic PTCH1 mutationAmir Hossein Saeidian, Adam Cohen-Nowak, Megan O'Donnell, et al.
JID Innovations : Skin Science From Molecules to Population Health|July 12, 2024
Whole-Transcriptome Sequencing-Based Profiling of the Cutaneous Virome in Patients with Secondary ImmunodeficiencyLeila Youssefian, Amir Hossein Saeidian, Zahra Saffarian, et al.
Orphanet Journal of Rare Diseases|July 26, 2019
Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patientsSara Guerrero-Aspizua, Claudio J Conti, Maria Jose Escamez, et al.
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