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    Research 121–150 of 1000+

    1. Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families ˜The œjournal of gene medicine · 2020 · 3 citations
    2. Genetic and hormonal influence on SARS-CoV-2-infection susceptibility Annals of Oncology · 2020 · 2 citations
    3. Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi Animal Genetics · 2024 · 1 citations
    4. Does Complement Have a Role in the Pathogenesis of Alopecia Areata? Skin appendage disorders · 2018 · 1 citations
    5. Trichodystrophies: A hair-raising differential diagnosis Clinics in Dermatology · 2015 · 1 citations
    6. XX/XY chimerism in tortoiseshell tomcats – a new case and review of the literature Sexual Development · 2026
    7. Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging Journal of Investigative Dermatology · 2024
    8. The First Visit: Consult and Workup Before Sperm Banking Springer eBooks · 2017
    9. A Clinical Study of 50 Cases of Female Pattern Hair Loss Journal of Diagnosis and Therapy on Dermato-venereology · 2011
    10. A Study of the androgen receptor gene polymorphism and the level of expression of the androgen receptor in androgenetic alopecia among Egyptians Egyptian Journal of Medical Human Genetics · 2009
    11. DNA phenotyping: current application in forensic science Research and reports in forensic medical science · 2019 · 11 citations
    12. Simultaneous Typing of Erythrocyte Acid Phosphatase, Adenylate Kinase and Adenosine Deaminase in Human Hair Root Sheaths Journal of the Forensic Science Society · 1986 · 1 citations
    13. From the Microscopic Sweat Gland to Large Datasets: The Power of Quantitative Traits in Dermatology Journal of Investigative Dermatology · 2024
    14. PEDL-XAI: A Hybrid Probabilistic Ensemble Deep Learning Approach for Hair Disorder Diagnosis International Journal of Engineering Research and Science & Technology · 2026
    15. 606 Connecting signaling dynamics with cell fates in live mice Journal of Investigative Dermatology · 2021
    16. Uncombable hair syndrome and beyond Acta dermatovenerologica Alpina, Pannonica et Adriatica (Tiskana izd.) · 2022
    17. Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases PLOS Genetics · 2012 · 87 citations
    18. Combing the genome for the root cause of baldness Nature Genetics · 2008 · 7 citations
    19. Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1 Journal of Dermatological Science · 2010 · 4 citations
    20. Genomic Analysis of Trichotillomania medRxiv · 2025 · 1 citations
    21. Comprehensive whole-genome resequencing unveils genetic diversity and selective signatures of the Xiangdong black goat Frontiers in genetics · 2024
    22. Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits International journal of molecular sciences · 2024
    23. ANALYSIS OF CTLA 4 GENE +49A/G AND CT60 A/G POLYMORPHISMS IN ALOPECIA AREATA PATIENTS Sabuncuoglu Serefeddin Health Sciences · 2023
    24. Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination Frontiers in Genetics · 2025 · 2 citations
    25. The genetic basis of dermatophytosis skin infection susceptibility Nature Communications · 2026
    26. Regulatory pathway analysis of coat color genes in Mongolian horses Hereditas · 2017 · 14 citations
    27. Prioritizing Susceptibility Genes for the Prognosis of Male-pattern Baldness with Transcriptome-wide Association Study Research Square (Research Square) · 2024
    28. Exome-wide age-of-onset analysis reveals exonic variants in ERN1, TACR3 and SPPL2C associated with Alzheimer’s disease bioRxiv (Cold Spring Harbor Laboratory) · 2020
    29. Past, Present and Future Perspectives of Forensic Genetics Biomolecules · 2025 · 8 citations
    30. Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease Translational Psychiatry · 2021 · 12 citations