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    Research 871–900 of 1000+

    1. Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis BMC Medical Genomics · 2021 · 47 citations
    2. The nude gene and the skin Experimental Dermatology · 2001 · 41 citations
    3. Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment Cells · 2019 · 39 citations
    4. Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex The American Journal of Human Genetics · 2012 · 39 citations
    5. Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages Frontiers in Microbiology · 2019 · 37 citations
    6. High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry Cell Genomics · 2023 · 31 citations
    7. Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed Genes · 2020 · 27 citations
    8. Stem Cell Therapies for Epidermolysis Bullosa Treatment Bioengineering · 2023 · 22 citations
    9. Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers Journal of Investigative Dermatology · 2023 · 21 citations
    10. A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics Biology · 2023 · 20 citations
    11. Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer Cancers · 2021 · 20 citations
    12. Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic? Reviews in endocrine and metabolic disorders · 2021 · 19 citations
    13. Report from the Cicatricial Alopecia Colloquium Journal of Investigative Dermatology · 2006 · 15 citations
    14. Recent omics advances in hair aging biology and hair biomarkers analysis Ageing Research Reviews · 2023 · 7 citations
    15. Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study The application of clinical genetics · 2019 · 6 citations
    16. A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits BMC genomics · 2023 · 5 citations
    17. Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature Life · 2023 · 5 citations
    18. How Our Microbiome Influences the Pathogenesis of Alopecia Areata Genes · 2022 · 4 citations
    19. Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex Veterinary Pathology · 2023 · 2 citations
    20. Claves diagnósticas en displasias pilosas II 2021 · 2 citations
    21. A Comprehensive Review of GWASs of Human Hair Traits Journal of Investigative Dermatology · 2025 · 1 citations
    22. Causes and therapeutic limitations of clinical alopecia and the advent of human pluripotent stem cell follicular transplantation Stem Cell Research & Therapy · 2025 · 1 citations
    23. Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep Animals · 2024 · 1 citations
    24. Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins IntechOpen eBooks · 2021 · 1 citations
    25. Montagna Symposium 2016—The Skin: Our Sensory Organ for Itch, Pain, Touch, and Pleasure 2017 · 1 citations
    26. Innovations in skin microphysiological systems for nonclinical testing and FDA modernization Microsystems & Nanoengineering · 2026
    27. Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome Dermatopathology · 2025
    28. Immortality Reconsidered: Clinical Challenges at the Frontier of Plastic Surgery Journal of Clinical Medicine · 2025
    29. Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection Biomedicines · 2025
    30. A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene 2024