1. The mitochondrial DNA 4977‐bp deletion and copy number alteration in Han Chinese samples with uterine fibroids
   Yong Luo et al, 2019, Annals of Human Genetics CrossRef
2. Novel TRERF1 mutations in Chinese patients with ovarian endometriosis
   Bianna Cao et al, 2018, Molecular Medicine Reports CrossRef
3. The presence of KRAS, PPP2R1A and ARID1A mutations in 101 Chinese samples with ovarian endometriosis
   Yang Zou et al, 2018, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis CrossRef
4. Mediator Kinase Disruption in MED12-Mutant Uterine Fibroids From Hispanic Women of South Texas
   Min Ju Park et al, 2018, The Journal of Clinical Endocrinology & Metabolism CrossRef
5. Variants in exon 2 of MED12 gene causes uterine leiomyoma’s through over-expression of MMP-9 of ECM pathway
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6. The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review
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7. Novel MYH8 mutations in 152 Han Chinese samples with ovarian endometriosis
   Jun Lou et al, 2020, Gynecological Endocrinology CrossRef
8. Stem Cell Growth and Differentiation in Organ Culture: New Insights for Uterine Fibroid Treatment
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9. Identification of a novel ESR1 mutation in a Chinese PCOS woman with estrogen insensitivity in IVF treatment
   Faying Liu et al, 2022, Reproductive Biology and Endocrinology CrossRef
10. MED12 is frequently mutated in ovarian and other adnexal leiomyomas
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11. Frequency of MED12 Mutation in Relation to Tumor and Patient’s Clinical Characteristics: a Meta-analysis
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12. Novel CTCF mutations in Chinese patients with ovarian endometriosis
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13. Understanding Obesity as a Risk Factor for Uterine Tumors Using Drosophila
    Xiao Li et al, 2019, The Drosophila Model in Cancer CrossRef