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    Research 421–450 of 1000+

    1. The diagnosis and treatment of iron deficiency and its potential relationship to hair loss Journal of The American Academy of Dermatology · 2006 · 207 citations
    2. Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase PLoS Genetics · 2010 · 73 citations
    3. Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation Journal of Cellular Biochemistry · 2011 · 37 citations
    4. <i>WNT10A</i> , dermatology and dentistry British Journal of Dermatology · 2021 · 30 citations
    5. <i>Hedychium spicatum</i>: a systematic review on traditional uses, phytochemistry, pharmacology and future prospectus Journal of Pharmacy and Pharmacology · 2018 · 30 citations
    6. What does acne genetics teach us about disease pathogenesis? British Journal of Dermatology · 2019 · 29 citations
    7. Reversible Alopecia Universalis During Treatment with PEG-Interferon and Ribavirin for Chronic Hepatitis C Journal of Chemotherapy · 2005 · 27 citations
    8. Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease 2018 · 26 citations
    9. Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias Experimental Dermatology · 2018 · 22 citations
    10. PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS) Anticancer Research · 2018 · 21 citations
    11. Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study PLoS ONE · 2019 · 12 citations
    12. Irreversible alopecia universalis during treatment with pegylated interferon-ribavirin for chronic hepatitis C virus infection: Case report and published work review Hepatology Research · 2012 · 9 citations
    13. Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3 Cellular immunology · 2015 · 8 citations
    14. Disease causing homozygous variants in the human hairless gene International Journal of Dermatology · 2015 · 7 citations
    15. Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum Neurodegenerative Diseases · 2018 · 7 citations
    16. Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele Journal of the European Academy of Dermatology and Venereology · 2009 · 6 citations
    17. Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels PloS one · 2018 · 4 citations
    18. Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study Cancer Causes & Control · 2017 · 4 citations
    19. Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study Clinical Cosmetic and Investigational Dermatology · 2024 · 2 citations
    20. Episodic Neuropathic-Like Musculoskeletal Pain Associated With Ritlecitinib Therapy in Alopecia Universalis: A Case Report Cureus · 2025 · 1 citations
    21. Understanding Polycystic Ovary Syndrome Directory of Open access Books (OAPEN Foundation) · 2025
    22. Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study Research Square (Research Square) · 2022
    23. 643 Male pattern baldness and risk of incident skin cancer in a cohort of men Journal of Investigative Dermatology · 2016
    24. Regulation of VDR by ΔNp63α is associated with inhibition of cell invasion Journal of Cell Science · 2009 · 34 citations
    25. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations
    26. The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor Genes & Development · 2001 · 178 citations
    27. Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering PLoS Biology · 2011 · 103 citations
    28. The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis PLoS Genetics · 2012 · 99 citations
    29. A Mouse Model of Androgenetic Alopecia Endocrinology · 2010 · 42 citations
    30. Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity Developmental Biology · 2008 · 28 citations