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    1. Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report Frontiers in Genetics · 2025
    2. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex Nature · 2010 · 199 citations
    3. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex American journal of human genetics · 2018 · 55 citations
    4. Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex The American Journal of Human Genetics · 2012 · 39 citations
    5. A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family Journal of Cutaneous Pathology · 2010 · 7 citations
    6. Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach JAAD Case Reports · 2024
    7. Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2% Journal of Dermatological Treatment · 2023
    8. Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors Dermatologic Therapy · 2022
    9. BIOACTIVE AND PERIPHERAL ANDROGENS IN PREPUBERTAL SIMPLE HYPERTRICHOSIS Clinical Endocrinology · 1990 · 11 citations
    10. Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient Journal of dermatology · 2013 · 2 citations
    11. Diffuse congenital hypotrichosis simplex with associated hair shaft fragility Australasian Journal of Dermatology · 2021 · 1 citations
    12. Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family Dermatology Reports · 2011 · 1 citations
    13. Autosomal recessive hereditary hypotrichosis simplex: A case report JAAD Case Reports · 2024
    14. Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis PLoS ONE · 2014 · 21 citations
    15. Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes American Journal of Medical Genetics Part A · 2021 · 16 citations
    16. A rare clinical image of hypertrichosis (Werewolf syndrome) ˜The œPan African medical journal · 2022
    17. Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses European Journal of Dermatology · 2011 · 83 citations
    18. ‘Black dots’ seen under trichoscopy are not specific for alopecia areata Clinical and Experimental Dermatology · 2012 · 42 citations
    19. Corneodesmosin: Structure, Function and Involvement in Pathophysiology The Open Dermatology Journal · 2010 · 2 citations
    20. Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations Cells · 2023
    21. Genetics of Structural Hair Disorders Journal of Investigative Dermatology · 2012 · 17 citations
    22. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    23. Hair: more than just an appendage International journal of research in dermatology · 2021
    24. Editors' Picks Journal of Investigative Dermatology · 2010
    25. News in brief Expert Review of Dermatology · 2010
    26. Spironolactone therapy in hypertrichosis European journal of endocrinology · 1996 · 4 citations
    27. Minoxidil-Induced Hypertrichosis Southern Medical Journal · 1977 · 46 citations
    28. Eccrine angiomatous hamartoma Dermatology Online Journal · 2006 · 8 citations
    29. Congenital hypotrichosis due to short anagen British Journal of Dermatology · 2000 · 42 citations
    30. Congenital atrichia and hypotrichosis World Journal of Pediatrics · 2011 · 11 citations