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    Research 271–300 of 1000+

    1. Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review American Journal of Medical Genetics Part A · 2021 · 10 citations
    2. Azathioprine‐induced severe myelosuppression accompanied by massive hair loss and painful oral ulcer in an autoimmune hepatitis patient with <i>NUDT15</i> minor variant: A case report Clinical Case Reports · 2021 · 3 citations
    3. Low-Dose Dimethyl Sulfoxide (DMSO) Suppresses Androgen Receptor (AR) and Its Splice Variant AR-V7 in Castration-Resistant Prostate Cancer (CRPC) Cells Therapeutics · 2025
    4. Frontal Fibrosing Alopecia and Increased Scalp Sweating: Is Neurogenic Inflammation the Common Link Skin Appendage Disorders · 2015 · 15 citations
    5. Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene Journal of Molecular Neuroscience · 2022 · 9 citations
    6. Do we need hair follicle stem cells and hair follicle neogenesis to cure common hair loss disorders? Hair transplant forum international · 2008 · 3 citations
    7. Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients Translational Andrology and Urology · 2022
    8. Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases PLOS Genetics · 2012 · 87 citations
    9. Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants Frontiers in Genetics · 2024 · 13 citations
    10. A Novel In Vivo Active Pemphigus Model Targeting Desmoglein1 and Desmoglein3: A Tool Representing All Pemphigus Variants Biology · 2023 · 2 citations
    11. Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations The American Journal of Surgical Pathology · 2021 · 4 citations
    12. 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
    13. Rooster feathering, androgenic alopecia, and hormone-dependent tumor growth: What is in common? Differentiation · 2004 · 23 citations
    14. The Physiological Impact of Melatonin, Its Effect on the Course of Diseases and Their Therapy and the Effect of Magnetic Fields on Melatonin Secretion—Potential Common Pathways of Influence Biomolecules · 2024 · 3 citations
    15. Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss Archives of Dermatological Research · 2013 · 21 citations
    16. MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes bioRxiv (Cold Spring Harbor Laboratory) · 2020 · 2 citations
    17. Exploiting molecular genetic diagnoses of polycystic ovary syndrome to achieve better patient outcome Murdoch Research Repository (Murdoch University) · 2018
    18. Atrichia With Papular Lesions Archives of Dermatology · 1986 · 32 citations
    19. A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer PLOS Genetics · 2020 · 43 citations
    20. Self-reported long COVID-19 symptoms are rare among vaccinated healthcare workers Journal of Infection and Public Health · 2023 · 14 citations
    21. Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep Journal of Advanced Research · 2023 · 2 citations
    22. An overview of JAK/STAT pathways and JAK inhibition in alopecia areata Frontiers in immunology · 2022 · 40 citations
    23. Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review Endocrine Connections · 2026
    24. From the Microscopic Sweat Gland to Large Datasets: The Power of Quantitative Traits in Dermatology Journal of Investigative Dermatology · 2024
    25. Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata Frontiers in endocrinology · 2024
    26. Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications Journal of Genome Biotechnology and Genetics · 2026
    27. High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort Journal of the Endocrine Society · 2022 · 2 citations
    28. A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice Neurobiology of aging · 2008 · 62 citations
    29. Immunological aspects and gender bias during respiratory viral infections including novel Coronavirus disease‐19 (COVID‐19): A scoping review Journal of Medical Virology · 2021 · 11 citations
    30. GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction Journal of Investigative Dermatology · 2023 · 4 citations