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Masoud Zabihi

Observed names: M. Zabihi, Zabihi, Masoud
ORCID: 0000-0002-7372-6318
Observed ORCID: 0000-0002-7372-6318
OpenAlex ID: A5101488798
Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity
2021 · Leila Youssefian, Amir Hossein Saeidian, et al. · Clinical Chemistry · 33
Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation
2021 · Hassan Vahidnezhad, Leila Youssefian, et al. · Matrix Biology · 9
Keratitis‐ichthyosis‐deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p. Asp50Asn GJB2 mutation
2020 · Tina Asgari, Mahtab Naji, et al. · Dermatologic Therapy · 7
Ichthyosis follicularis syndromes in patients with mutations in GJB2
2022 · Leila Youssefian, Mahtab Naji, et al. · Clinical and Experimental Dermatology · 5
Perceived Stress among Iranians during COVID-19 Pandemic; Stressors and Coping Mechanisms: A Mixed-methods Approach
2021 · Masoomeh Faghankhani, Faezeh Sodagari, et al. · The Canadian Journal of Psychiatry · 4
186 Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation
2021 · H. Vahidnezhad, L. Youssefian, et al. · Journal of Investigative Dermatology · 2
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185 GJB2 mutations in patients with ichthyosis follicularis and histopathology of porokeratotic adnexal ostial nevus
2021 · L. Youssefian, F. Abdollahimajd, et al. · Journal of Investigative Dermatology
Works count: 9
Citation count: 60
H-index: 4
I10-index: 1
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