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    Research 931–960 of 1000+

    1. KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies European journal of human genetics · 2022 · 3 citations
    2. Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination Frontiers in Genetics · 2025 · 2 citations
    3. High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort Journal of the Endocrine Society · 2022 · 2 citations
    4. Regulation and dysregulation of hair regeneration: aiming for clinical application Cell Regeneration · 2022 · 2 citations
    5. A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle Genes · 2021 · 2 citations
    6. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    7. Forging the Future: 2018 Alopecia Areata Research Summit Summary Report Journal of Investigative Dermatology Symposium Proceedings · 2020 · 1 citations
    8. The Association Between Polycystic Ovary Syndrome and Its Dermatological Manifestations Cureus · 2020 · 1 citations
    9. Montagna Symposium 2016—The Skin: Our Sensory Organ for Itch, Pain, Touch, and Pleasure 2017 · 1 citations
    10. First Symposium of Ichthyosis Experts 2013 · 1 citations
    11. Pathological Skin Scarring: From Mechanism to Targeted Local Therapy Preprints.org · 2026
    12. Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review Endocrine Connections · 2026
    13. Unravelling the threads of central centrifugal cicatricial alopecia Journal of Investigative Dermatology · 2026
    14. 5α-Reductase Isoenzymes: From Neurosteroid Biosynthesis to Neuropsychiatric Outcomes NeuroSci · 2026
    15. An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves BMC Veterinary Research · 2026
    16. The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs BMC Genomics · 2025
    17. Immortality Reconsidered: Clinical Challenges at the Frontier of Plastic Surgery Journal of Clinical Medicine · 2025
    18. Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report American Journal of Case Reports · 2025
    19. Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities Cureus · 2025
    20. Clinical and demographic characteristics of frontal fibrosing alopecia in a dermatology referral center in Bogota, Colombia: a descriptive cross-sectional study International Journal of Women’s Dermatology · 2024
    21. A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene 2024
    22. Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study Clinical Cosmetic and Investigational Dermatology · 2024
    23. Effects of Biomaterials Derived from Germinated Hemp Seeds on Stressed Hair Stem Cells and Immune Cells International Journal of Molecular Sciences · 2024
    24. Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study Human genomics · 2024
    25. Stable isotope analyses of carbon and nitrogen in hair keratin of suspected man-eating wolves from 1880s Scientific Reports · 2024
    26. Insights into Alopecia Areata: A Systematic Review of Prevalence, Pathogenesis, and Psychological Consequences ˜The œOpen dermatology journal · 2024
    27. Clinical guidelines of ukrainian hair research society. diagnosis and treatment of alopecia areata Aktualʹnì problemi sučasnoï medicini · 2023
    28. Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss Clinical, Cosmetic and Investigational Dermatology · 2023
    29. A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2 Revista Paulista de Pediatria · 2023
    30. Pathogenesis of androgenetic alopecia 2022