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    1. Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility 2009 · 189 citations
    2. Keratinization and its Disorders Oman Medical Journal · 2012 · 95 citations
    3. A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders Experimental Dermatology · 2026
    4. Congenital and Hereditary Skin Diseases 2018
    5. Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs PLoS ONE · 2012 · 28 citations
    6. Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex Journal of Investigative Dermatology · 2017 · 44 citations
    7. Anatomical and Dermatologic Manifestations of Estrogen Deficiency in Postmenopausal Women: A Systematic Review Pakistan Journal of Health Sciences · 2025
    8. 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility Journal of Investigative Dermatology · 2017
    9. Skin Disorders in Transgender Patients 2023
    10. Dermatological manifestations in patients with chronic kidney disease International journal of dermatology, venereology and leprosy sciences · 2019
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