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    Research 241–270 of 1000+

    1. A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients Breast cancer research · 2013 · 32 citations
    2. The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71 Mammalian genome · 2010 · 75 citations
    3. Keratin 71 Mutations: From Water Dogs to Woolly Hair 2012 · 11 citations
    4. The impact of certain genetic variants (single nucleotide polymorphisms) on incidence and severity of COVID‐19 ˜The œjournal of gene medicine · 2021 · 7 citations
    5. A review of genetic researches of and rogenic alopecia Int J Genet · 2016
    6. Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study African Journal of Urology · 2023 · 4 citations
    7. Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family Journal of Investigative Dermatology · 2012 · 52 citations
    8. Characterization of novel TMEM173 mutation with additive IFIH1 risk allele bioRxiv (Cold Spring Harbor Laboratory) · 2018 · 1 citations
    9. A mutation in MAP2 is associated with prenatal hair follicle density The FASEB Journal · 2019 · 11 citations
    10. A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females Nature Communications · 2015 · 103 citations
    11. 9. Immunology and Genetics Medical & surgical dermatology · 2009
    12. Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene Mammalian Genome · 2022
    13. Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans Journal of Interferon & Cytokine Research · 2014 · 22 citations
    14. Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep Gene · 2012 · 51 citations
    15. A mechanism-informed deep neural network enables prioritization of regulators that drive cell state transitions Nature Communications · 2025 · 13 citations
    16. Androgen receptor CAG repeat length is associated with ovarian reserve but not with ovarian response Reproductive Biomedicine Online · 2014 · 7 citations
    17. Sex dependent influence of a functional polymorphism in steroid 5‐α‐reductase type 2 (<i>SRD5A2</i>) on post‐traumatic stress symptoms American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2013 · 35 citations
    18. Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women Human Reproduction · 2006 · 25 citations
    19. Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults F1000Research · 2021 · 5 citations
    20. Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults F1000Research · 2021 · 2 citations
    21. MTHFR C677T Polymorphism and Serum Homocysteine Level as Risk Factors of Coronary Heart Disease in Patients with Androgenetic Alopecia: A Case Control Study The American Journal of the Medical Sciences · 2021
    22. Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes 2005 · 53 citations
    23. Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men Cancer Epidemiology, Biomarkers & Prevention · 2014 · 9 citations
    24. Supplementary Material for: Polymorphic CAG Repeat Numbers in the Androgen Receptor Gene of Female Pattern Hair Loss in a Han Chinese Population 2016
    25. Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia Journal of Dermatological Science · 2003 · 15 citations
    26. Variation in the ovine trichohyalin gene and its association with wool curvature Small Ruminant Research · 2017 · 8 citations
    27. Association Between Retinoid X Receptor Gene Variants and Dyslipidemia Risk in an Iranian Population Cureus · 2021 · 1 citations
    28. 034 Characterization of novel TMEM173 mutation causing a lupus- and SAVI-like phenotype, modified by polymorphisms in TMEM173 and IFIH1 2019
    29. Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse TSpace · 2009
    30. Cloning and Expression of Cellular Retinoic Acid Binding Protein I Gene in Inner Mongolian Cashmere Goats 2012 · 1 citations