1. Hill, Holly A, Qi, Xinyue, Jain, Preetesh, Zhou, Shouhao, Wang, Michael L. . Genetic mutations and features of mantle cell lymphoma: a systematic review and meta-analysis. In Blood advances, 4, 2927-2938. doi:10.1182/bloodadvances.2019001350. https://pubmed.ncbi.nlm.nih.gov/32598477/
2. Li, Xuan, Cai, Du, Huang, Yaoyi, Yu, Huichuan, Wang, Xiaolin. 2023. Aberrant methylation in neurofunctional gene serves as a hallmark of tumorigenesis and progression in colorectal cancer. In BMC cancer, 23, 315. doi:10.1186/s12885-023-10765-x. https://pubmed.ncbi.nlm.nih.gov/37020199/
3. Snyder, Kara, Dixon, C Edward, Henchir, Jeremy, Kochanek, Patrick M, Jackson, Travis C. 2024. Gene knockout of RNA binding motif 5 in the brain alters RIMS2 protein homeostasis in the cerebellum and Hippocampus and exacerbates behavioral deficits after a TBI in mice. In Experimental neurology, 374, 114690. doi:10.1016/j.expneurol.2024.114690. https://pubmed.ncbi.nlm.nih.gov/38218585/
4. Wang, Xiong, Xie, Jiazhao, Tan, Lu, Li, Xiaoguang, Cheng, Liming. 2023. N6-methyladenosine-modified circRIMS2 mediates synaptic and memory impairments by activating GluN2B ubiquitination in Alzheimer's disease. In Translational neurodegeneration, 12, 53. doi:10.1186/s40035-023-00386-6. https://pubmed.ncbi.nlm.nih.gov/38012808/
5. Siddiq, Mustafa M, Toro, Carlos A, Johnson, Nicholas P, Cardozo, Christopher P, Iyengar, Ravi. 2023. Spinal cord injury regulates circular RNA expression in axons. In Frontiers in molecular neuroscience, 16, 1183315. doi:10.3389/fnmol.2023.1183315. https://pubmed.ncbi.nlm.nih.gov/37692100/
6. Mechaussier, Sabrina, Almoallem, Basamat, Zeitz, Christina, De Baere, Elfride, Perrault, Isabelle. 2020. Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement. In American journal of human genetics, 106, 859-871. doi:10.1016/j.ajhg.2020.04.018. https://pubmed.ncbi.nlm.nih.gov/32470375/