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    1. Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity. UNC Libraries · 2020 · 32 citations
    2. Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness 2022
    3. Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness eLife · 2022 · 16 citations
    4. Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness bioRxiv (Cold Spring Harbor Laboratory) · 2021 · 2 citations
    5. Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness 2022
    6. Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak BMC genomics · 2022
    7. A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities Archives of Dermatological Research · 2012 · 6 citations
    8. Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia Human Genetics · 2007 · 60 citations
    9. Cloning and sequence analysis of KAP 6.1 gene in Xinjiang fine-wool sheep Heilongjiang xumu shouyi · 2013
    10. Molecular characterisation of keratin-associated protein-7 (KRTAP7) gene for hair quality in Indian Dromedary Camel 2024
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