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    Research 901–930 of 1000+

    1. Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia Dermatology Online Journal · 2021
    2. Muir-torre syndrome in two families in Leicestershire, United Kingdom Journal of the American Academy of Dermatology · 2005
    3. Hair follicle culture—a historical perspective Hair transplant forum international · 2013 · 1 citations
    4. Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review Clinical Medicine Insights Case Reports · 2025
    5. Polycystic ovary syndrome Nature Reviews Disease Primers · 2024 · 292 citations
    6. Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management. PubMed · 2022 · 188 citations
    7. Adult female acne: a guide to clinical practice Anais Brasileiros de Dermatologia · 2019 · 164 citations
    8. The Pathobiology of Skin Aging American Journal Of Pathology · 2020 · 122 citations
    9. Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats Journal of Heredity · 2007 · 75 citations
    10. A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice Neurobiology of aging · 2008 · 62 citations
    11. Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26 American Journal of Human Genetics · 2008 · 62 citations
    12. Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations Scientific reports · 2018 · 58 citations
    13. Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument Journal of toxicologic pathology · 2013 · 53 citations
    14. Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis 2013 · 51 citations
    15. Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment International Journal of Women's Dermatology · 2019 · 38 citations
    16. Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed Genes · 2020 · 27 citations
    17. Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome The Journal of Clinical Endocrinology & Metabolism · 2002 · 27 citations
    18. The Implication of Neuroactive Steroids in Tourette's Syndrome Pathogenesis: A Role for 5α‐Reductase? Journal of neuroendocrinology · 2013 · 24 citations
    19. Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers Journal of Investigative Dermatology · 2023 · 21 citations
    20. New developments in the molecular treatment of ichthyosis: review of the literature Orphanet journal of rare diseases · 2022 · 21 citations
    21. New approach to the understanding of keloid: psychoneuroimmune–endocrine aspects Clinical Cosmetic and Investigational Dermatology · 2015 · 21 citations
    22. Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic? Reviews in endocrine and metabolic disorders · 2021 · 19 citations
    23. Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector Stem Cell Research & Therapy · 2013 · 18 citations
    24. Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models Frontiers in Oncology · 2024 · 17 citations
    25. Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease Translational Psychiatry · 2021 · 12 citations
    26. Female pattern hair loss—An update Indian Dermatology Online Journal · 2020 · 12 citations
    27. The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015 Endocrine Reviews · 2024 · 10 citations
    28. The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes International journal of molecular sciences · 2021 · 10 citations
    29. Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review Journal of Clinical Medicine · 2024 · 6 citations
    30. A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients BMC Medical Genetics · 2020 · 6 citations