1. Barbier, Mathieu, Camuzat, Agnès, Hachimi, Khalid El, Brice, Alexis, Le Ber, Isabelle. . SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration. In Brain : a journal of neurology, 144, 2798-2811. doi:10.1093/brain/awab171. https://pubmed.ncbi.nlm.nih.gov/34687211/
2. Zhu, Huiqiong, Xiong, Hailin, Guo, Xuli, Liao, Haojie, Zhang, Shuyi. 2024. SLITRK2 as a prognostic and immunological biomarker in gastric cancer. In Discover oncology, 15, 667. doi:10.1007/s12672-024-01534-8. https://pubmed.ncbi.nlm.nih.gov/39550447/
3. Afsar, Tayyaba, Fu, Hongxia, Khan, Hammal, Razak, Suhail, Umair, Muhammad. 2024. Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder. In Frontiers in genetics, 14, 1308116. doi:10.3389/fgene.2023.1308116. https://pubmed.ncbi.nlm.nih.gov/38283150/
4. Ma, Shengchao, Long, Li, Huang, Xixia, Wu, Cuiling, Zhao, Zhiwen. 2023. Transcriptome analysis reveals genes associated with wool fineness in merinos. In PeerJ, 11, e15327. doi:10.7717/peerj.15327. https://pubmed.ncbi.nlm.nih.gov/37250719/
5. Salesse, Charleen, Charest, Julien, Doucet-Beaupré, Hélène, De Koninck, Paul, Lévesque, Martin. . Opposite Control of Excitatory and Inhibitory Synapse Formation by Slitrk2 and Slitrk5 on Dopamine Neurons Modulates Hyperactivity Behavior. In Cell reports, 30, 2374-2386.e5. doi:10.1016/j.celrep.2020.01.084. https://pubmed.ncbi.nlm.nih.gov/32075770/
6. Fazeli, Zahra, Ghaderian, Sayyed Mohammad Hossein, Najmabadi, Hossein, Omrani, Mir Davood. 2022. Understanding the Molecular Basis of Fragile X Syndrome Using Differentiated Mesenchymal Stem Cells. In Iranian journal of child neurology, 16, 85-95. doi:10.22037/ijcn.v15i4.22070. https://pubmed.ncbi.nlm.nih.gov/35222660/
7. Aruga, Jun, Mikoshiba, Katsuhiko. . Identification and characterization of Slitrk, a novel neuronal transmembrane protein family controlling neurite outgrowth. In Molecular and cellular neurosciences, 24, 117-29. doi:. https://pubmed.ncbi.nlm.nih.gov/14550773/