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    Research 391–420 of 494

    1. A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients Breast cancer research · 2013 · 32 citations
    2. Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology Genetics research international · 2018 · 29 citations
    3. Male pattern baldness and prostate cancer risk in a population-based case–control study Cancer epidemiology · 2010 · 29 citations
    4. The role of WNT10B in physiology and disease: A 10-year update Frontiers in Cell and Developmental Biology · 2023 · 27 citations
    5. 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
    6. Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep Open Journal of Genetics · 2011 · 26 citations
    7. The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans SpringerPlus · 2014 · 25 citations
    8. Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency Journal of Investigative Dermatology · 2014 · 24 citations
    9. Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer Cancers · 2021 · 20 citations
    10. Age-related changes in the dorsal skin histology in Mini and Wistar rats. PubMed · 2002 · 20 citations
    11. Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss EBioMedicine · 2020 · 19 citations
    12. The molecular pathogenesis of Trichilemmal carcinoma BMC Cancer · 2020 · 19 citations
    13. Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development Biology Direct · 2016 · 19 citations
    14. Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat PloS one · 2020 · 16 citations
    15. Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction International Journal of Molecular Sciences · 2015 · 16 citations
    16. Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study BMJ Open · 2019 · 15 citations
    17. Transposon control as a checkpoint for tissue regeneration Development · 2022 · 14 citations
    18. Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease Cell Reports · 2022 · 14 citations
    19. Regulatory pathway analysis of coat color genes in Mongolian horses Hereditas · 2017 · 14 citations
    20. Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review Indian Journal of Dermatology · 2016 · 13 citations
    21. Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research Journal of Investigative Dermatology · 2021 · 12 citations
    22. Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata Journal of Clinical Laboratory Analysis · 2018 · 12 citations
    23. Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder Indian dermatology online journal · 2013 · 12 citations
    24. Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women Bioscience Reports · 2019 · 11 citations
    25. Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature Jaypee's international journal of clinical pediatric dentistry · 2018 · 11 citations
    26. Tabby pattern genetics – a whole new breed of cat Pigment Cell & Melanoma Research · 2010 · 11 citations
    27. Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype Journal of Investigative Dermatology · 2007 · 11 citations
    28. Skin morphology of the mutant hairless USP mouse Brazilian Journal of Medical and Biological Research · 2005 · 11 citations
    29. Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research Animals · 2024 · 10 citations
    30. The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes International journal of molecular sciences · 2021 · 10 citations