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    1. Clinical and molecular genetic studies in hereditary hair loss 2021
    2. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis Nature Genetics · 2009 · 181 citations
    3. The genetics of hair shaft disorders Journal of The American Academy of Dermatology · 2008 · 59 citations
    4. Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless Journal of Investigative Dermatology · 2000 · 29 citations
    5. Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family 2007 · 25 citations
    6. A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities Archives of Dermatological Research · 2012 · 6 citations
    7. Marie-unna hereditary hypotrichosis International Journal of Trichology · 2014 · 4 citations
    8. Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless Journal of Investigative Dermatology · 2000 · 4 citations
    9. Current Genetics in Hair Diseases InTech eBooks · 2013 · 1 citations
    10. Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report European Journal of Dermatology · 2018
    11. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    12. Dermatopathology and molecular genetics Journal of The American Academy of Dermatology · 2008 · 12 citations
    13. Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles Journal of Investigative Dermatology · 2012 · 5 citations
    14. Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit) Journal of complementary medicine & alternative healthcare · 2023
    15. The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i> JAMA dermatology · 2014 · 22 citations
    16. Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis Cell Stem Cell · 2021 · 23 citations
    17. A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions Human Genetics · 2019 · 10 citations
    18. Hair physiology and its disorders Drug Discovery Today: Disease Mechanisms · 2008 · 31 citations
    19. Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm Journal of Investigative Dermatology · 2011 · 26 citations
    20. The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits ˜The œFASEB journal · 2018 · 18 citations
    21. Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin Genetics in medicine · 2018 · 10 citations
    22. A review of genotrichoses and hair pathology associated with inherited skin diseases British Journal of Dermatology · 2023 · 8 citations
    23. Alopezien und Hypotrichosen im Kindesalter Der Hautarzt · 2014 · 5 citations
    24. Woolly hair generalizado: caso clínico e revisão da literatura Journal Archives of Health · 2024
    25. Pathology in Practice Journal of the American Veterinary Medical Association · 2018
    26. Cutaneous drug reactions Elsevier eBooks · 2010 · 1 citations
    27. Hipertricose generalizada exuberante em um lactente: relato de caso Residência Pediátrica · 2024
    28. Συχνότητα και μελέτη του δασυτριχισμού στον ελληνικό πληθυσμό 2004
    29. Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity Clinical Cosmetic and Investigational Dermatology · 2025
    30. Two females with hair loss Journal der Deutschen Dermatologischen Gesellschaft · 2019