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    Research 481–510 of 1000+

    1. Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children Archives of Dermatology · 1992 · 55 citations
    2. Prolactin: an emerging force along the cutaneous–endocrine axis Trends in Endocrinology and Metabolism · 2010 · 51 citations
    3. Improving translational research in sex-specific effects of comorbidities and risk factors in ischaemic heart disease and cardioprotection: position paper and recommendations of the ESC Working Group on Cellular Biology of the Heart Cardiovascular Research · 2020 · 47 citations
    4. The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation The Journal of Clinical Endocrinology and Metabolism · 2014 · 47 citations
    5. Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us? Experimental Dermatology · 2016 · 46 citations
    6. Association of premature hair graying with family history, smoking, and obesity: A cross-sectional study Journal of The American Academy of Dermatology · 2014 · 46 citations
    7. Female type of adult acne: Physiological and psychological considerations and management Journal der Deutschen Dermatologischen Gesellschaft · 2018 · 42 citations
    8. Congenital hypotrichosis due to short anagen British Journal of Dermatology · 2000 · 42 citations
    9. Dermatologic Features of Classic Movie Villains JAMA Dermatology · 2017 · 41 citations
    10. Objective outcome measures: Collecting meaningful data on alopecia areata Journal of The American Academy of Dermatology · 2017 · 39 citations
    11. Male pattern baldness and the risk of prostate cancer Annals of Oncology · 2011 · 38 citations
    12. Morphological Approach to Hair Disorders Journal of Investigative Dermatology Symposium Proceedings · 2003 · 38 citations
    13. Facial Hair Restoration Facial Plastic Surgery Clinics of North America · 2013 · 37 citations
    14. De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes European Journal of Human Genetics · 2019 · 36 citations
    15. Circulatory Changes in Alopecia Archives of Dermatology · 1961 · 36 citations
    16. Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia Postepy Dermatologii I Alergologii · 2014 · 35 citations
    17. Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis Journal of Investigative Dermatology · 2013 · 32 citations
    18. Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism* The Journal of Clinical Endocrinology and Metabolism · 1997 · 31 citations
    19. Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations Journal of Clinical Immunology · 2021 · 30 citations
    20. Re-Evaluating Cyclosporine A as a Hair Growth–Promoting Agent in Human Scalp Hair Follicles Journal of Investigative Dermatology · 2015 · 29 citations
    21. How to Diagnose Hair Loss Dermatologic Clinics · 2012 · 27 citations
    22. Idiopathic CD4+ T-lymphocytopenia The Lancet · 1992 · 27 citations
    23. Trichotillomania in children and adolescents: Review of the literature and case report Child Psychiatry & Human Development · 1990 · 27 citations
    24. Sperm aneuploidy in infertile male patients: a systematic review of the literature Andrologia · 2014 · 26 citations
    25. Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases? BioEssays · 2014 · 26 citations
    26. Expression of<i>Sfrp2</i>Is Increased in Catagen of Hair Follicles and Inhibits Keratinocyte Proliferation Annals of Dermatology · 2014 · 25 citations
    27. Guidelines for the Use of Acitretin in Psoriasis Actas Dermo-Sifiliográficas · 2013 · 25 citations
    28. Riboflavin-responsive glutaryl CoA dehydrogenase deficiency Molecular Genetics and Metabolism · 2005 · 25 citations
    29. Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype PLOS genetics · 2019 · 24 citations
    30. Lymphomatoid granulomatosis Journal of the American Academy of Dermatology · 1992 · 24 citations