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    Research 661–690 of 762

    1. The Role of Nrf2 in Hearing Loss Frontiers in Pharmacology · 2021 · 17 citations
    2. Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides Forensic Science International Genetics · 2020 · 17 citations
    3. Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction International Journal of Molecular Sciences · 2015 · 16 citations
    4. Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations PloS one · 2014 · 15 citations
    5. Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging American Journal of Medical Genetics - Part A · 2013 · 15 citations
    6. Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms Fertility and sterility · 2010 · 15 citations
    7. Molecular cloning, characterization, and expression of sheep FGF5 gene Gene · 2014 · 11 citations
    8. Sex-limited chromosomes and non-reproductive traits BMC Biology · 2022 · 10 citations
    9. Molecular Mechanisms Lead to Sex-Specific COVID-19 Prognosis and Targeted Therapies Frontiers in Medicine · 2020 · 10 citations
    10. Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene Journal of Molecular Neuroscience · 2022 · 9 citations
    11. Allopregnanolone Alters the Gene Expression Profile of Human Glioblastoma Cells International journal of molecular sciences · 2018 · 9 citations
    12. Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss Archives of Dermatological Research · 2012 · 9 citations
    13. Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population Molecular genetics and metabolism reports · 2019 · 8 citations
    14. Sustained Postnatal Skin Regeneration Upon Prenatal Application of Functionalized Collagen Scaffolds Tissue Engineering Part A · 2019 · 8 citations
    15. Are 2D:4D finger-length ratios an indicator of androgenetic alopecia in males? Anais Brasileiros De Dermatologia · 2016 · 8 citations
    16. Selenium Compounds and Their Bioactivities: Molecular Mechanisms and Prospects for Functional Food and Therapeutic Applications Plants · 2025 · 7 citations
    17. Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak Frontiers in Genetics · 2022 · 7 citations
    18. Hormonal interventions in skin wounds – a mini review Molecular Medicine · 2024 · 6 citations
    19. Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families BMC Ophthalmology · 2024 · 6 citations
    20. Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses BMC genomics · 2023 · 6 citations
    21. Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens) Gene · 2022 · 6 citations
    22. Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation BMC Medical Genomics · 2022 · 6 citations
    23. CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico Anais Brasileiros de Dermatologia · 2020 · 6 citations
    24. The causal relationship between gut microbiota and alopecia areata: a Mendelian randomization analysis Frontiers in Microbiology · 2024 · 5 citations
    25. Genetic Variants and Protective Immunity against SARS-CoV-2 Genes · 2022 · 5 citations
    26. Use of Antiandrogens as Therapeutic Agents in COVID-19 Patients Viruses · 2022 · 5 citations
    27. An update of polycystic ovary syndrome: causes and therapeutics options Heliyon · 2022 · 5 citations
    28. Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk Bioscience Reports · 2020 · 5 citations
    29. Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin Archives of Dermatological Research · 2019 · 5 citations
    30. Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease PloS one · 2019 · 5 citations