1. Chen, Ying, Li, Bingxun, Xu, Hongxuan, Wu, Lin. 2024. Causal gene identification using mitochondria-associated genome-wide mendelian randomization in atrial fibrillation. In Frontiers in pharmacology, 15, 1439816. doi:10.3389/fphar.2024.1439816. https://pubmed.ncbi.nlm.nih.gov/39135799/
2. Wu, Jihao, Chen, Xiong, Li, Ruijun, Li, Yanbing, Huang, Yinong. 2024. Identifying genetic determinants of sarcopenia-related traits: a Mendelian randomization study of druggable genes. In Metabolism: clinical and experimental, 160, 155994. doi:10.1016/j.metabol.2024.155994. https://pubmed.ncbi.nlm.nih.gov/39117060/
3. Gumus, Evren, Temiz, Ebru, Sarikaya, Baran, Sipahioglu, Serkan, Gonel, Ataman. 2020. The Association Between BMP-2, UQCC1 and CX3CR1 Polymorphisms and the Risk of Developmental Dysplasia of the Hip. In Indian journal of orthopaedics, 55, 169-175. doi:10.1007/s43465-020-00235-y. https://pubmed.ncbi.nlm.nih.gov/33569111/
4. Yang, Aruhan, Zhu, Xiaoxue, Zhang, Lei, Ding, Yanhua, Lv, Guoyue. 2022. Non-invasive evaluation of NAFLD and the contribution of genes: an MRI-PDFF-based cross-sectional study. In Hepatology international, 16, 1035-1051. doi:10.1007/s12072-022-10355-2. https://pubmed.ncbi.nlm.nih.gov/35829866/
5. Mullin, Benjamin H, Zhu, Kun, Brown, Suzanne J, Xu, Jiake, Wilson, Scott G. . Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis. In Genetics, 225, . doi:10.1093/genetics/iyad150. https://pubmed.ncbi.nlm.nih.gov/37579195/
智鼠故事 
