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    Research 10 of 87

    1. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations
    2. Phenotypic variability associated with<i>WNT10A</i>nonsense mutations 2010 · 28 citations
    3. The fundamentals of WNT10A Differentiation · 2025 · 6 citations
    4. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    5. N02. Hair and Nails Australasian Journal of Dermatology · 1997
    6. Molecular basis of hypohidrotic ectodermal dysplasia: an update Journal of Applied Genetics · 2015 · 85 citations
    7. Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements Journal of Human Genetics · 2016 · 30 citations
    8. Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia Orphanet Journal of Rare Diseases · 2026
    9. Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i> The Journal of Dermatology · 2017 · 5 citations
    10. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
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