1. Tang, Jue, Liu, Wei, Zhu, Jinhong, Xia, Huimin, He, Jing. 2018. RSRC1 and CPZ gene polymorphisms with neuroblastoma susceptibility in Chinese children. In Gene, 662, 83-87. doi:10.1016/j.gene.2018.04.015. https://pubmed.ncbi.nlm.nih.gov/29653227/
2. Potkin, Steven G, Macciardi, Fabio, Guffanti, Guia, Vawter, Marquis P, Xie, Xiaohui. 2010. Identifying gene regulatory networks in schizophrenia. In NeuroImage, 53, 839-47. doi:10.1016/j.neuroimage.2010.06.036. https://pubmed.ncbi.nlm.nih.gov/20600988/
3. Yu, Shijun, Gautam, Nishim, Quan, Ming, Gao, Yong. 2019. RSRC1 suppresses gastric cancer cell proliferation and migration by regulating PTEN expression. In Molecular medicine reports, 20, 1747-1753. doi:10.3892/mmr.2019.10409. https://pubmed.ncbi.nlm.nih.gov/31257492/
4. Perez, Yonatan, Menascu, Shay, Cohen, Idan, Yeger-Lotem, Esti, Birk, Ohad S. . RSRC1 mutation affects intellect and behaviour through aberrant splicing and transcription, downregulating IGFBP3. In Brain : a journal of neurology, 141, 961-970. doi:10.1093/brain/awy045. https://pubmed.ncbi.nlm.nih.gov/29522154/
5. Xia, Jingjing, Chen, Sheng, Zhang, Zhujian, Wang, Jipeng. 2023. Identification of a novel RSRC1-ALK (R6: A20) fusion using next-generation sequencing technique. In Cancer genetics, 278-279, 18-23. doi:10.1016/j.cancergen.2023.08.003. https://pubmed.ncbi.nlm.nih.gov/37572583/
6. Scala, Marcello, Mojarrad, Majid, Riazuddin, Saima, Houlden, Henry, Maroofian, Reza. . RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability. In Brain : a journal of neurology, 143, e31. doi:10.1093/brain/awaa070. https://pubmed.ncbi.nlm.nih.gov/32227164/
7. Potkin, S G, Turner, J A, Fallon, J A, Guffanti, G, Macciardi, F. 2008. Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia. In Molecular psychiatry, 14, 416-28. doi:10.1038/mp.2008.127. https://pubmed.ncbi.nlm.nih.gov/19065146/
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