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    Research 511–540 of 1000+

    1. Polycystic Ovarian Syndrome in Adolescents Cureus · 2023 · 16 citations
    2. Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging American Journal of Medical Genetics - Part A · 2013 · 15 citations
    3. Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study PLoS ONE · 2019 · 12 citations
    4. Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema Dermatology · 2015 · 11 citations
    5. Hair, Hormones, and High-Risk Prostate Cancer Journal of Clinical Oncology · 2014 · 3 citations
    6. Hyperandrogenism in Women: Polycystic Ovary Syndrome Hanyang Medical Reviews · 2012 · 3 citations
    7. Anagen Effluvium in Association With Extracorporeal Membrane Oxygenation Pediatric Dermatology · 2017 · 2 citations
    8. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    9. The Role of Histone Demethylases in Disease Springer eBooks · 2011 · 1 citations
    10. Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese 2022
    11. 574 Murine sebaceous gland homeostasis requires intact cutaneous innervation in a hair cycle-dependent context 2019
    12. 573 Hair follicles employ a 2-dimensional healing strategy to repair 3-dimensional injuries 2019
    13. Follikelhormone Springer Reference Medizin · 2019
    14. Androgen effects on the skin Cambridge University Press eBooks · 2015
    15. The pathogenesis of alopecia areata 2015
    16. First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy Clinical Biochemistry · 2007
    17. Obesity and the skin British Journal of Dermatology · 2011 · 128 citations
    18. Keratin disorders: from gene to therapy 2011 · 109 citations
    19. The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis PLoS Genetics · 2012 · 99 citations
    20. Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype PLOS genetics · 2019 · 24 citations
    21. 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
    22. An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice Human & Experimental Toxicology · 2016
    23. Genetic Variation at the MC1R Locus and the Time since Loss of Human Body Hair Current anthropology · 2004 · 152 citations
    24. Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research Journal of Neuroendocrinology · 2015 · 123 citations
    25. Adverse effects of common medications on male fertility Nature Reviews Urology · 2015 · 77 citations
    26. Alopecia areata: a review on diagnosis, immunological etiopathogenesis and treatment options Clinical and Experimental Medicine · 2021 · 56 citations
    27. Absorption sites of orally administered drugs in the small intestine Expert Opinion on Drug Discovery · 2017 · 55 citations
    28. Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes Scientific Reports · 2017 · 54 citations
    29. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    30. A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents Frontiers in Medicine · 2017 · 40 citations