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    Research 9 of 259

    1. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex Nature · 2010 · 199 citations
    2. 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
    3. Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach JAAD Case Reports · 2024
    4. Hair: more than just an appendage International journal of research in dermatology · 2021
    5. Severe Variant of X‐linked Dyskeratosis Congenita (Hoyeraal‐Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy Journal of Pediatric Gastroenterology and Nutrition · 2009 · 26 citations
    6. A mechanical-assisted post-bioprinting strategy for challenging bone defects repair Nature Communications · 2024 · 48 citations
    7. Correlation Between In Vivo Reflectance Confocal Microscopy and Horizontal Histopathology in Skin Cancer: A Review Frontiers in oncology · 2021 · 13 citations
    8. A Mechanical-assisted Post-bioprinting Strategy for Challenging Bone Defects Repair Research Square (Research Square) · 2023 · 1 citations
    9. The efficacy of a photolyase-based device on the cancerization field: a clinical and thermographic study Journal of Experimental & Clinical Cancer Research · 2015 · 16 citations
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