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    Research 91–120 of 1000+

    1. Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men Human Genetics and Genomics Advances · 2025
    2. Androgenetic Alopecia in Men: An Update On Genetics Indian Journal of Dermatology · 2024
    3. Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors Frontiers in Veterinary Science · 2022 · 2 citations
    4. Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition Stem Cell Reviews and Reports · 2021 · 12 citations
    5. Genome-wide association study in alopecia areata implicates both innate and adaptive immunity Nature · 2010 · 717 citations
    6. Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans American journal of human genetics · 2009 · 234 citations
    7. Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair Nature genetics · 2008 · 210 citations
    8. Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata The American Journal of Human Genetics · 2007 · 143 citations
    9. The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans SpringerPlus · 2014 · 25 citations
    10. Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition Genes · 2019 · 14 citations
    11. Bloom's syndrome–‐a first report from India International Journal of Dermatology · 2000 · 13 citations
    12. The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes International journal of molecular sciences · 2021 · 10 citations
    13. The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears Veterinary Dermatology · 2008 · 10 citations
    14. Atrichia with papular lesions International journal of trichology · 2011 · 8 citations
    15. Marie-unna hereditary hypotrichosis International Journal of Trichology · 2014 · 4 citations
    16. A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia Genesis · 2012 · 4 citations
    17. Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality BMC Genomics · 2023 · 1 citations
    18. Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish Frontiers in Endocrinology · 2022
    19. Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene Mammalian Genome · 2022
    20. Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia International Journal of Molecular Medicine · 2012 · 28 citations
    21. Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones Neuropsychopharmacology · 2019 · 197 citations
    22. Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters European Journal of Human Genetics · 2023 · 1 citations
    23. Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis Clinical Immunology · 2022 · 41 citations
    24. Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response Molecular cytogenetics · 2014 · 5 citations
    25. Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep Animals · 2024 · 3 citations
    26. Genetic mechanism of androgenic alopecia International Journal of Dermatology and Venereology · 2009
    27. Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up Movement Disorders · 2011 · 39 citations
    28. Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice Journal of Investigative Dermatology · 2010 · 23 citations
    29. Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies Movement Disorders · 2011 · 17 citations
    30. A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL Genes · 2026