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    1. Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot Human Genome Variation · 2026
    2. Polymorphisms in the promoter regions of the CXCL1 and CXCL2 genes contribute to increased risk of alopecia areata in the Korean population Genetics and Molecular Research · 2015 · 8 citations
    3. Correlation and regression analysis of the <i>KRT27</i> and <i>ELOVL4</i> genes in cashmere fineness and other production performances in Liaoning cashmere goats 2025
    4. The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women Journal of Assisted Reproduction and Genetics · 2014 · 28 citations
    5. Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness Human Genetics · 2009 · 42 citations
    6. Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia Gene · 2020 · 9 citations
    7. Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA bioRxiv (Cold Spring Harbor Laboratory) · 2018 · 6 citations
    8. Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study Clinical Cosmetic and Investigational Dermatology · 2024 · 2 citations
    9. COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine Mayo Clinic Proceedings · 2020 · 58 citations
    10. Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA eLife · 2019 · 49 citations
    11. Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep Genes · 2024
    12. Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases Molecular Neurodegeneration · 2024 · 26 citations
    13. <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome Journal of Clinical Laboratory Analysis · 2024 · 6 citations
    14. Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes BMC Genomics · 2024 · 13 citations
    15. DKK4 as a novel candidate marker for Zhexi Angora rabbit wool quality World Rabbit Science · 2026
    16. Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders Frontiers in Immunology · 2020 · 20 citations
    17. Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population The Application of Clinical Genetics · 2021 · 3 citations
    18. Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement Genes · 2024
    19. Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review Journal of Obstetrics and Gynaecology Research · 2017 · 36 citations
    20. Topische Immuntherapie mit Diphenylcyclopropenon bei verschiedenen Typen der Alpecia areata: Assoziation zu klinischen Parametern und einem funktionellen Genpolymorphismus des Interleukin-6-Promotors Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · 2005
    21. Genome-Wide Association Study of Fiber Diameter in Alpacas Animals · 2023 · 1 citations
    22. IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep Small Ruminant Research · 2026
    23. Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research Animals · 2024 · 10 citations
    24. The Telomerase Reverse Transcriptase (TERT) Gene Molecular Characterization in Sheep and the Association of Its Variation with Wool Traits Animals · 2026
    25. The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism Scientific Reports · 2022
    26. Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency Journal of Investigative Dermatology · 2014 · 24 citations
    27. The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle Animal Genetics · 2007 · 51 citations
    28. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis Nature Genetics · 2009 · 181 citations
    29. The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications Forensic Sciences · 2024
    30. Episodic Neuropathic-Like Musculoskeletal Pain Associated With Ritlecitinib Therapy in Alopecia Universalis: A Case Report Cureus · 2025 · 1 citations