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    Research 301–330 of 1000+

    1. Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders International Journal of Molecular Sciences · 2025
    2. The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy Frontiers in Pharmacology · 2024
    3. Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population Frontiers in Genetics · 2024
    4. Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement Genes · 2024
    5. C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata Skin research and technology · 2024
    6. Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata Frontiers in endocrinology · 2024
    7. Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness Animals · 2023
    8. Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome ˜The œJournal of clinical endocrinology and metabolism · 2023
    9. Endocrinology Clinical Chemistry and Laboratory Medicine · 2023
    10. The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism Scientific Reports · 2022
    11. A Profuse Pipeline of Promising Options Sustainable development goals series · 2022
    12. A perspective on predictive markers of alopecia Archives of Medicine and Health Sciences · 2020
    13. Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases Molecular Neurodegeneration · 2024 · 26 citations
    14. Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults F1000Research · 2021 · 2 citations
    15. Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients Medicina · 2024 · 1 citations
    16. Eziopatogenesi e terapia dell'acne:studio epidemiologico delle caratteristiche cliniche di una popolazione di pazienti affetti da acne e analisi dei polimorfismi del gene codificante per il recettore degli androgeni e del gene codificante per il citocromo P-450 1A1 Padua Research Archive (University of Padua) · 2008
    17. The JAK/STAT signaling pathway: from bench to clinic Signal Transduction and Targeted Therapy · 2021 · 489 citations
    18. Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities Signal Transduction and Targeted Therapy · 2022 · 318 citations
    19. Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis The Scientific World Journal · 2014 · 291 citations
    20. The resistance mechanisms of bacteria against ciprofloxacin and new approaches for enhancing the efficacy of this antibiotic Frontiers in Public Health · 2022 · 238 citations
    21. The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted Current Biology · 1998 · 153 citations
    22. Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata The American Journal of Human Genetics · 2007 · 143 citations
    23. Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis Dermatology Online Journal · 2013 · 78 citations
    24. SHISA6 Confers Resistance to Differentiation-Promoting Wnt/β-Catenin Signaling in Mouse Spermatogenic Stem Cells Stem Cell Reports · 2017 · 77 citations
    25. New clinico‐genetic classification of trichothiodystrophy American Journal of Medical Genetics Part A · 2009 · 68 citations
    26. STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity Orphanet Journal of Rare Diseases · 2014 · 65 citations
    27. Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans Veterinary pathology · 2010 · 56 citations
    28. DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration PLOS ONE · 2010 · 56 citations
    29. Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis American journal of human genetics · 2019 · 53 citations
    30. Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA eLife · 2019 · 49 citations