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    Research 811–840 of 1000+

    1. The impact of certain genetic variants (single nucleotide polymorphisms) on incidence and severity of COVID‐19 ˜The œjournal of gene medicine · 2021 · 7 citations
    2. Biomedical applications of organoids in genetic diseases Medical Review · 2024
    3. Molecular Genetic and Endocrine Mechanisms of Hair Growth Hormone Research in Paediatrics · 2003 · 51 citations
    4. Quantitative Models for the Study of Hair Growth <i>in Vivo</i><sup>a</sup> Annals of the New York Academy of Sciences · 1991 · 34 citations
    5. Dermatopathology and molecular genetics Journal of The American Academy of Dermatology · 2008 · 12 citations
    6. Analysis of breast health outcomes in women on oral 5-alpha reductase inhibitors: A single-center retrospective cohort study Journal of the American Academy of Dermatology · 2024 · 6 citations
    7. Risk of autoimmune thyroid diseases in individuals with alopecia areata: A nationwide case‐control study JDDG Journal der Deutschen Dermatologischen Gesellschaft · 2025 · 1 citations
    8. Identificación de la variación molecular y genética subyacente a las enfermedades de la piel Repository of Digital Objects for Teaching Research and Culture (University of Valencia) · 2025
    9. Diversifying the case study: How far has physiology education come in integrating equality, diversity and inclusion into the curricula? Physiology News · 2021
    10. https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/# 2020
    11. Cyberspace Chat: Beyond genetics part III: evidence that lifestyle choices may impact hair loss in androgenetic alopecia Hair transplant forum international · 2012
    12. Green Technologies in the Generic Pharmaceutical Industry 2010 · 10 citations
    13. Development of polycystic ovary syndrome: involvement of genetic and environmental factors Andrology · 2005 · 232 citations
    14. Deep facial mycosis due to <i>Trichophyton verrucosum</i>—molecular genetic identification of the dermatophyte in paraffin‐embedded tissue—case report and review of the literature Mycoses · 2017 · 11 citations
    15. A new familial presentation of dissecting cellulitis: The genetic implications on scarring alopecias JAAD Case Reports · 2020 · 9 citations
    16. BH26 First reported case of lichen planopilaris in siblings: evidence for a genetic link? British Journal of Dermatology · 2025
    17. Hypotrichosis with juvenile macular dystrophy: a case report with molecular study 2018
    18. A Theoretical Model for the Treatment of Androgenetic Alopecia Using the STEAP3 Protein, and the Genetic Challenges of Treating AGA Health Science Reports · 2026
    19. Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study Frontiers in Medicine · 2026
    20. Auto-portrait as self-evaluation and follow-up of androgenetic alopecia: A case study Journal of The European Academy of Dermatology and Venereology · 1998
    21. An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves BMC Veterinary Research · 2026
    22. LSD1 is Required for Hair Cell Regeneration in Zebrafish Molecular Neurobiology · 2015 · 28 citations
    23. Inhibition of Bmp signaling affects growth and differentiation in the anagen hair follicle The EMBO Journal · 2000 · 305 citations
    24. Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men Cell Stem Cell · 2020 · 139 citations
    25. Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture The American Journal of Human Genetics · 2010 · 97 citations
    26. Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia Journal of Investigative Dermatology · 1999 · 66 citations
    27. Lineage Analysis of Epidermal Stem Cells Cold Spring Harbor Perspectives in Medicine · 2014 · 57 citations
    28. The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects Developmental Dynamics · 2006 · 49 citations
    29. Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair Journal of Investigative Dermatology · 2009 · 34 citations
    30. Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5 Genomics · 2003 · 29 citations