1. Wang, Ya, Tan, Jie, Liu, Dan, Yang, Yameng, Wu, Hongyan. 2019. The Association of UNC13B Gene Polymorphisms and Diabetic Kidney Disease in a Chinese Han Population. In Medical science monitor : international medical journal of experimental and clinical research, 25, 8527-8533. doi:10.12659/MSM.919930. https://pubmed.ncbi.nlm.nih.gov/31713534/
2. Wang, Jie, Qiao, Jing-Da, Liu, Xiao-Rong, Gu, Wei-Yue, Liao, Wei-Ping. . UNC13B variants associated with partial epilepsy with favourable outcome. In Brain : a journal of neurology, 144, 3050-3060. doi:10.1093/brain/awab164. https://pubmed.ncbi.nlm.nih.gov/33876820/
3. Trégouet, David-Alexandre, Groop, Per-Henrik, McGinn, Steven, Lathrop, Mark, Vionnet, Nathalie. 2008. G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes. In Diabetes, 57, 2843-50. doi:10.2337/db08-0073. https://pubmed.ncbi.nlm.nih.gov/18633107/
4. Egawa, Jun, Hoya, Satoshi, Watanabe, Yuichiro, Iwata, Nakao, Someya, Toshiyuki. 2016. Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study. In American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 171, 797-805. doi:10.1002/ajmg.b.32444. https://pubmed.ncbi.nlm.nih.gov/26990377/
5. Xu, Dafeng, Wang, Yu, Liu, Xiangmei, Chen, Liang, Zheng, Jinfang. 2020. Development and clinical validation of a novel 9-gene prognostic model based on multi-omics in pancreatic adenocarcinoma. In Pharmacological research, 164, 105370. doi:10.1016/j.phrs.2020.105370. https://pubmed.ncbi.nlm.nih.gov/33316381/
6. Lauterbach, Edward C. 2012. Psychotropic drug effects on gene transcriptomics relevant to Parkinson's disease. In Progress in neuro-psychopharmacology & biological psychiatry, 38, 107-15. doi:10.1016/j.pnpbp.2012.03.011. https://pubmed.ncbi.nlm.nih.gov/22507762/
7. Jenny Zhou, Huanjiao, Qin, Lingfeng, Zhang, Haifeng, Wu, Dianqing, Min, Wang. 2016. Endothelial exocytosis of angiopoietin-2 resulting from CCM3 deficiency contributes to cerebral cavernous malformation. In Nature medicine, 22, 1033-1042. doi:10.1038/nm.4169. https://pubmed.ncbi.nlm.nih.gov/27548575/
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