1. Sayed, Jamal, Gamal, Ahmed, Theyab, Abdulrahman, Algahtani, Mohamed, Aldaadi, Banan Bakheet. 2023. Neonatal rhizomelic chondrodysplasia punctata type 2 caused by a novel homozygous variant in the GNPAT gene. In Clinical case reports, 11, e7504. doi:10.1002/ccr3.7504. https://pubmed.ncbi.nlm.nih.gov/37323250/
2. Gu, Li, Zhu, Yahui, Lin, Xi, Prochownik, Edward V, Li, Youjun. 2018. Amplification of Glyceronephosphate O-Acyltransferase and Recruitment of USP30 Stabilize DRP1 to Promote Hepatocarcinogenesis. In Cancer research, 78, 5808-5819. doi:10.1158/0008-5472.CAN-18-0340. https://pubmed.ncbi.nlm.nih.gov/30143522/
3. Levstik, Alexander, Stuart, Alan, Adams, Paul C. . GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis. In Annals of hepatology, 15, 907-910. doi:. https://pubmed.ncbi.nlm.nih.gov/27740525/
4. Rishi, Gautam, Secondes, Eriza S, Asplett, Kiran, Berger, Johannes, Subramaniam, V Nathan. . Dysregulated hepcidin response to dietary iron in male mice with reduced Gnpat expression. In Bioscience reports, 40, . doi:10.1042/BSR20201508. https://pubmed.ncbi.nlm.nih.gov/32766721/
5. Yang, Zhaohui, Bai, Caijuan, Pu, Youwei, Qi, Xuebin, Su, Bing. 2022. Genetic adaptation of skin pigmentation in highland Tibetans. In Proceedings of the National Academy of Sciences of the United States of America, 119, e2200421119. doi:10.1073/pnas.2200421119. https://pubmed.ncbi.nlm.nih.gov/36161951/
6. McLaren, Christine E, Emond, Mary J, Subramaniam, V Nathan, Anderson, Gregory J, McLaren, Gordon D. 2015. Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload. In Hepatology (Baltimore, Md.), 62, 429-39. doi:10.1002/hep.27711. https://pubmed.ncbi.nlm.nih.gov/25605615/
7. Jang, Jung Eun, Park, Han-Sol, Yoo, Hyun Ju, Koh, Eun Hee, Lee, Ki-Up. 2017. Protective role of endogenous plasmalogens against hepatic steatosis and steatohepatitis in mice. In Hepatology (Baltimore, Md.), 66, 416-431. doi:10.1002/hep.29039. https://pubmed.ncbi.nlm.nih.gov/28073164/
8. Zhang, Qi-Hao, Zhang, Yan, He, Rui-Xuan, Guo, Han-Ming, Wang, Xin-Guang. 2022. Anatomical characteristics and potential gene mutation sites of a familial recurrent patellar dislocation. In BMC medical genomics, 15, 176. doi:10.1186/s12920-022-01330-9. https://pubmed.ncbi.nlm.nih.gov/35934709/
9. Liu, Yu-Li, Fann, Cathy Shen-Jang, Liu, Chih-Min, Lee, Sandy F C, Hwu, Hai-Gwo. . A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention. In Biological psychiatry, 60, 554-62. doi:. https://pubmed.ncbi.nlm.nih.gov/16997000/
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