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    Research 91–120 of 1000+

    1. Reclassification of Botryococcus braunii chemical races into separate species based on a comparative genomics analysis PLoS ONE · 2024 · 8 citations
    2. De novo assembly and annotation of Asiatic lion (<i>Panthera leo persica</i>) genome bioRxiv (Cold Spring Harbor Laboratory) · 2019 · 2 citations
    3. Whole-genome sequencing of eight goat populations for the detection of selection signatures underlying production and adaptive traits Scientific Reports · 2016 · 92 citations
    4. Mechanisms and cell lineages in lymphatic vascular development Angiogenesis · 2021 · 43 citations
    5. Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep Genes · 2026
    6. Rare Gli1+ perivascular fibroblasts promote skin wound repair bioRxiv (Cold Spring Harbor Laboratory) · 2022 · 2 citations
    7. Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds BMC Veterinary Research · 2021 · 55 citations
    8. Predicting Human Appearance from DNA for Forensic Investigations Security science and technology · 2016 · 5 citations
    9. Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review Egyptian Journal of Medical Human Genetics · 2019 · 49 citations
    10. Ehlers-Danlos syndrome: From bedside to bench Frontiers research topics · 2024
    11. Essential resources and best practices for laboratory mouse research Molecules and Cells · 2025 · 4 citations
    12. Host-microbiome interactions and recent progress into understanding the biology of acne vulgaris Microbiome · 2018 · 194 citations
    13. 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
    14. Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism Meta Gene · 2018
    15. Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome Genes · 2019 · 20 citations
    16. The first 20 years of skin of color dermatology: An era of advancements in skin, hair, and nail disorders JAAD reviews. · 2025 · 1 citations
    17. Under‐Explored Species, Breeds and Cell Types With Potential for Cultivated Meat Production Food Bioengineering · 2026
    18. Tackling underrepresentation to aid understanding of Parkinson’s disease: Progress and further opportunities Physiology News · 2021
    19. Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family 2002 · 48 citations
    20. Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat Animals · 2024 · 15 citations
    21. Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks Genes · 2022 · 9 citations
    22. A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome Journal of The European Academy of Dermatology and Venereology · 2009 · 8 citations
    23. A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia Archives of Dermatological Research · 2015 · 2 citations
    24. Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep Animals · 2025 · 1 citations
    25. Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia DOAJ (DOAJ: Directory of Open Access Journals) · 2011 · 1 citations
    26. Determination of TG5 gene polymorphism and its influence on productivity traits of beef cattle reared in Lithuania Lithuanian University of Health Sciences · 2023
    27. Tackling underrepresentation to aid understanding of Parkinson’s disease: Progress and further opportunities Physiology News · 2021
    28. Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13 Journal of Biological Chemistry · 2004 · 47 citations
    29. Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene Yonsei Medical Journal · 2018 · 13 citations
    30. The Organizer and Beyond Cell · 2001 · 9 citations