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Publications by Hassan Vahidnezhad

Recessive Mutation in Tetraspanin CD151 Causes Kindler Syndrome-Like Epidermolysis Bullosa With Multi-Systemic Manifestations Including Nephropathy

Matrix Biology
Molecular Biology
2018English

Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families With High Degree of Customary Consanguineous Marriages

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2017English

Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2016English

Autosomal Recessive Congenital Ichthyosis: CERS3 Mutations Identified by a Next Generation Sequencing Panel Targeting Ichthyosis Genes

European Journal of Human Genetics
Genetics
2017English

Genome-Wide Single Nucleotide Polymorphism-Based Autozygosity Mapping Facilitates Identification of Mutations in Consanguineous Families With Epidermolysis Bullosa

Experimental Dermatology
BiochemistryDermatologyMolecular Biology
2018English

Assessment of the Risk and Characterization of Non-Melanoma Skin Cancer in Kindler Syndrome: Study of a Series of 91 Patients

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2019English

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