1. Liu, Yansong, Fu, Xiaoqian, Tang, Zhen, Zhou, Deyi, Zhu, Chunming. 2019. Altered expression of the CSMD1 gene in the peripheral blood of schizophrenia patients. In BMC psychiatry, 19, 113. doi:10.1186/s12888-019-2089-4. https://pubmed.ncbi.nlm.nih.gov/30987620/
2. Werren, Elizabeth A, Peirent, Emily R, Jantti, Henna, Srivastava, Anshika, Bielas, Stephanie L. 2024. Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations. In Cell death & disease, 15, 379. doi:10.1038/s41419-024-06768-6. https://pubmed.ncbi.nlm.nih.gov/38816421/
3. Bai, Xinling, Jin, Jianing, Li, Shanshan, Wang, Huimin, Xie, Anmu. 2021. CUB and Sushi Multiple Domains (CSMD1) Gene Polymorphisms and Susceptibilities to Idiopathic Parkinson's Disease in Northern Chinese Han Population: A Case-Control Study. In Parkinson's disease, 2021, 6661162. doi:10.1155/2021/6661162. https://pubmed.ncbi.nlm.nih.gov/33628416/
4. Wang, Xing, Chen, Xinwei, Liu, Yuanyuan, Sun, Zhenfeng, Chen, Lixiao. 2022. CSMD1 suppresses cancer progression by inhibiting proliferation, epithelial-mesenchymal transition, chemotherapy-resistance and inducing immunosuppression in esophageal squamous cell carcinoma. In Experimental cell research, 417, 113220. doi:10.1016/j.yexcr.2022.113220. https://pubmed.ncbi.nlm.nih.gov/35623420/
5. Damena, Delesa, Barry, Amadou, Morrison, Robert, Duffy, Patrick, Fried, Michal. 2024. A novel locus in CSMD1 gene is associated with increased susceptibility to severe malaria in Malian children. In Frontiers in genetics, 15, 1390786. doi:10.3389/fgene.2024.1390786. https://pubmed.ncbi.nlm.nih.gov/38854427/
6. Lee, Arthur S, Rusch, Jannette, Lima, Ana C, O'Bryan, Moira K, Conrad, Donald F. 2019. Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility. In Nature communications, 10, 4626. doi:10.1038/s41467-019-12522-w. https://pubmed.ncbi.nlm.nih.gov/31604923/