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    Research 361–390 of 1000+

    1. 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
    2. Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis Clinical Cosmetic and Investigational Dermatology · 2025
    3. Understanding Polycystic Ovary Syndrome Directory of Open access Books (OAPEN Foundation) · 2025
    4. Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization 2024
    5. Gut Microbiota and Its Association with Alopecia Areata: Insights from a Two-Sample Mendelian Randomization Study Research Square (Research Square) · 2023
    6. Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles Frontiers in genetics · 2022
    7. Hair, Cutaneous Homeostasis and Stem Cell Functions Journal of Investigative Dermatology · 2014
    8. 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients Journal of The American Academy of Dermatology · 2020
    9. The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study Journal of Investigative Dermatology · 2017 · 15 citations
    10. Australasian Society for Dermatology Research Meeting, May 2007 Journal of Investigative Dermatology · 2007
    11. Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss Cell Stem Cell · 2007 · 688 citations
    12. Stem Cells and the Niche: A Dynamic Duo Cell Stem Cell · 2010 · 333 citations
    13. β-catenin Activity in the Dermal Papilla Regulates Morphogenesis and Regeneration of Hair Developmental Cell · 2010 · 314 citations
    14. Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells Gastroenterology · 2010 · 291 citations
    15. TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons 2009 · 286 citations
    16. Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D Molecular Endocrinology · 2002 · 277 citations
    17. Severe cutaneous adverse reactions to drugs The Lancet · 2017 · 273 citations
    18. Wnt Signaling in Skin Development, Homeostasis, and Disease Cold Spring Harbor Perspectives in Biology · 2012 · 260 citations
    19. Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study Fertility and Sterility · 1999 · 216 citations
    20. The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults Rheumatology · 2017 · 213 citations
    21. Dermal papilla cell number specifies hair size, shape and cycling and its reduction causes follicular decline Development · 2013 · 211 citations
    22. Dermatoses of pregnancy Journal of The American Academy of Dermatology · 2001 · 208 citations
    23. Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia American Journal of Human Genetics · 2005 · 195 citations
    24. Cutaneous signs in COVID ‐19 patients: A review Dermatologic Therapy · 2020 · 176 citations
    25. Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion Genes & Development · 2006 · 169 citations
    26. Sic Transit Gloria: Farewell to the Epidermal Transit Amplifying Cell? Cell Stem Cell · 2007 · 153 citations
    27. Complex Hair Cycle Domain Patterns and Regenerative Hair Waves in Living Rodents Journal of Investigative Dermatology · 2007 · 127 citations
    28. Keratin 17 null mice exhibit age- and strain-dependent alopecia Genes & Development · 2002 · 122 citations
    29. Targeting the Wnt pathways for therapies Molecular and cellular therapies · 2014 · 112 citations
    30. EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency European Journal of Human Genetics · 2020 · 94 citations