1. Lin, Wei-De, Tsai, Fuu-Jen, Chou, I-Ching. 2022. Current understanding of the genetics of tourette syndrome. In Biomedical journal, 45, 271-279. doi:10.1016/j.bj.2022.01.008. https://pubmed.ncbi.nlm.nih.gov/35042017/
2. Hatayama, Minoru, Katayama, Kei-Ichi, Kawahara, Yukie, Yoshikawa, Takeo, Aruga, Jun. 2022. SLITRK1-mediated noradrenergic projection suppression in the neonatal prefrontal cortex. In Communications biology, 5, 935. doi:10.1038/s42003-022-03891-y. https://pubmed.ncbi.nlm.nih.gov/36085162/
3. Du, Jung-Chieh, Chang, Man-Hsin, Yeh, Chen-Jiun, Chuang, Shu-Hui, Chiou, Lih-Chu. 2023. Pivotal Role of Slitrk1 in Adult Striatal Cholinergic Neurons in Mice: Implication in Tourette Syndrome. In Annals of neurology, , . doi:10.1002/ana.26805. https://pubmed.ncbi.nlm.nih.gov/37776102/
4. Melo-Felippe, Fernanda B, Fontenelle, Leonardo F, Kohlrausch, Fabiana B. 2018. Gene variations in PBX1, LMX1A and SLITRK1 are associated with obsessive-compulsive disorder and its clinical features. In Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 61, 180-185. doi:10.1016/j.jocn.2018.10.042. https://pubmed.ncbi.nlm.nih.gov/30377043/
5. Miranda, Debora M, Wigg, Karen, Kabia, E Mameisia, Sandor, Paul, Barr, Cathy L. . Association of SLITRK1 to Gilles de la Tourette Syndrome. In American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 150B, 483-6. doi:10.1002/ajmg.b.30840. https://pubmed.ncbi.nlm.nih.gov/18698576/