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Research 10 of 18

1. Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2 Journal of Dermatological Science · 2015
2. Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population Frontiers in Genetics · 2024
3. The importance of basonuclin 2 in adult mice and its relation to basonuclin 1 Mechanisms of Development · 2016 · 14 citations
4. Genome-wide association study of skin complex diseases Journal of Dermatological Science · 2012 · 25 citations
5. Genetics of Diabetes in Childhood Springer eBooks · 2003
6. Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family Frontiers in genetics · 2021 · 1 citations
7. Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia PLOS ONE · 2019 · 3 citations
8. Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods” Canadian journal of neurological sciences · 2021 · 1 citations
9. Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review Frontiers in endocrinology · 2024
10. Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia Frontiers in Medicine · 2023

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