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    Research 31–60 of 365

    1. Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm Journal of Investigative Dermatology · 2011 · 26 citations
    2. Disease causing homozygous variants in the human hairless gene International Journal of Dermatology · 2015 · 7 citations
    3. Reply Journal of Investigative Dermatology · 2000 · 2 citations
    4. A Newborn With Hair Loss Clinical pediatrics · 2013 · 1 citations
    5. Commonly associated disorders with complete scalp alopecia in early childhood: A review International journal of trichology · 2023
    6. Alopecia totalis in an infant Cosmoderma · 2023
    7. Hairless: A nuclear receptor corepressor essential for skin function Advances in developmental biology · 2006
    8. Congenital atrichia associated with nevus flammeus: A rare association Indian dermatology online journal · 2014 · 2 citations
    9. Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan Pakistan Journal of Zoology · 2020
    10. Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia Journal of Investigative Dermatology · 1999 · 66 citations
    11. Morphological Approach to Hair Disorders Journal of Investigative Dermatology Symposium Proceedings · 2003 · 38 citations
    12. A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers The American Journal of Human Genetics · 1998 · 83 citations
    13. Congenital Atrichia: A Case Report International journal of science and healthcare research · 2023
    14. Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup> Photochemistry and photobiology · 2008 · 10 citations
    15. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    16. Genetics of Structural Hair Disorders Journal of Investigative Dermatology · 2012 · 17 citations
    17. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    18. A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia Journal of Investigative Dermatology · 2002 · 26 citations
    19. Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene 2001 · 139 citations
    20. Mutation des menschlichen hairless -Gens bei Atrichia universalis Der Hautarzt · 1998 · 2 citations
    21. Congenital atrichia associated with situs inversus and mesocardia International journal of trichology · 2012 · 5 citations
    22. A review of genotrichoses and hair pathology associated with inherited skin diseases British Journal of Dermatology · 2023 · 8 citations
    23. Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases Indian Dermatology Online Journal · 2025
    24. Utility of trichoscopy Indian journal of dermatopathology and diagnostic dermatology · 2018 · 1 citations
    25. Footprints of the EADV: a meeting report from the 17th Congress of the European Academy of Dermatology and Venereology British Journal of Dermatology · 2009 · 4 citations
    26. Association of a polymorphism in the ornithine decarboxylase gene with male androgenetic alopecia Journal of The American Academy of Dermatology · 2005 · 5 citations
    27. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    28. Female Pattern Hair Loss and its Relationship to Permanent/Cicatricial Alopecia: A New Perspective Journal of Investigative Dermatology Symposium Proceedings · 2005 · 73 citations
    29. Regenerative medicine and hair loss: how hair follicle culture has advanced our understanding of treatment options for androgenetic alopecia Regenerative Medicine · 2013 · 23 citations
    30. Alopecia areata in a rhesus monkey (Macaca mulatta) Journal of Medical Primatology · 2007 · 16 citations