1. Greiner, Alexander M, Mehdi, Haider, Cevan, Chloe, Gutmann, Rebecca, London, Barry. 2024. The role of GPD1L, a sodium channel interacting gene, in the pathogenesis of Brugada Syndrome. In Frontiers in medicine, 10, 1159586. doi:10.3389/fmed.2023.1159586. https://pubmed.ncbi.nlm.nih.gov/38962240/
2. Leung, Philip K H, Das, Bibek, Cheng, Xiaoyu, Tarazi, Munir. 2023. Prognostic and Predictive Utility of GPD1L in Human Hepatocellular Carcinoma. In International journal of molecular sciences, 24, . doi:10.3390/ijms241713113. https://pubmed.ncbi.nlm.nih.gov/37685919/
3. Shrestha, Ketan, Onasanya, Adepeju Esther, Eisenberg, Iris, Meidan, Rina, Imbar, Tal. 2018. miR-210 and GPD1L regulate EDN2 in primary and immortalized human granulosa-lutein cells. In Reproduction (Cambridge, England), 155, 197-205. doi:10.1530/REP-17-0574. https://pubmed.ncbi.nlm.nih.gov/29301980/
4. Hao, Hongting, Yan, Sen, Zhao, Xinbo, Yuan, Yue, Li, Yue. 2022. Atrial myocyte-derived exosomal microRNA contributes to atrial fibrosis in atrial fibrillation. In Journal of translational medicine, 20, 407. doi:10.1186/s12967-022-03617-y. https://pubmed.ncbi.nlm.nih.gov/36064558/
5. Valdivia, Carmen R, Ueda, Kazuo, Ackerman, Michael J, Makielski, Jonathan C. 2009. GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A. In American journal of physiology. Heart and circulatory physiology, 297, H1446-52. doi:10.1152/ajpheart.00513.2009. https://pubmed.ncbi.nlm.nih.gov/19666841/
6. Yuan, Meng, Guo, Yi, Xia, Hong, Deng, Hao, Yuan, Lamei. 2021. Novel SCN5A and GPD1L Variants Identified in Two Unrelated Han-Chinese Patients With Clinically Suspected Brugada Syndrome. In Frontiers in cardiovascular medicine, 8, 758903. doi:10.3389/fcvm.2021.758903. https://pubmed.ncbi.nlm.nih.gov/34957250/