1. Hechmi, Meriem, Dallali, Hamza, Gharbi, Meriem, Barakat, Abdelhamid, Kefi, Rym. . Association of rs662799 variant and APOA5 gene haplotypes with metabolic syndrome and its components: a meta-analysis in North Africa. In Bioscience reports, 40, . doi:10.1042/BSR20200706. https://pubmed.ncbi.nlm.nih.gov/32725151/
2. Lin, Yen-Chun, Nunez, Veronica, Johns, Robin, Shiao, S Pamela K. . APOA5 Gene Polymorphisms and Cardiovascular Diseases: Metaprediction in Global Populations. In Nursing research, 66, 164-174. doi:10.1097/NNR.0000000000000207. https://pubmed.ncbi.nlm.nih.gov/28252576/
3. Au, Anthony, Griffiths, Lyn R, Irene, Looi, Kooi, Cheah Wee, Wei, Loo Keat. 2017. The impact of APOA5, APOB, APOC3 and ABCA1 gene polymorphisms on ischemic stroke: Evidence from a meta-analysis. In Atherosclerosis, 265, 60-70. doi:10.1016/j.atherosclerosis.2017.08.003. https://pubmed.ncbi.nlm.nih.gov/28865324/
4. Guo, Jiabao, Miao, Guolin, Zhang, Wenxi, Huang, Wei, Xian, Xunde. 2024. Depletion of ApoA5 aggravates spontaneous and diet-induced nonalcoholic fatty liver disease by reducing hepatic NR1D1 in hamsters. In Theranostics, 14, 2036-2057. doi:10.7150/thno.91084. https://pubmed.ncbi.nlm.nih.gov/38505614/
5. Pu, Na, Yang, Qi, Shi, Xiao-Lei, Li, Wei-Qin, Li, Jie-Shou. 2020. Gene-environment interaction between APOA5 c.553G>T and pregnancy in hypertriglyceridemia-induced acute pancreatitis. In Journal of clinical lipidology, 14, 498-506. doi:10.1016/j.jacl.2020.05.003. https://pubmed.ncbi.nlm.nih.gov/32561169/
6. Do, Ron, Stitziel, Nathan O, Won, Hong-Hee, Gabriel, Stacey, Kathiresan, Sekar. 2014. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. In Nature, 518, 102-6. doi:10.1038/nature13917. https://pubmed.ncbi.nlm.nih.gov/25487149/
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