1. Zhou, Hongfei, Diao, Mengyuan, Zhang, Mingyue. 2016. The Association between ANXA11 Gene Polymorphisms and Sarcoidosis: a Meta-Analysis and systematic review. In Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 33, 102-11. doi:. https://pubmed.ncbi.nlm.nih.gov/27537711/
2. Snyder, Allison, Ryan, Veronica H, Hawrot, James, Cookson, Mark R, Ward, Michael E. 2024. An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndrome. In Alzheimer's & dementia : the journal of the Alzheimer's Association, 20, 5220-5235. doi:10.1002/alz.13915. https://pubmed.ncbi.nlm.nih.gov/38923692/
3. Liu, Xiangyi, Wu, Chujun, He, Ji, Zhang, Nan, Fan, Dongsheng. 2018. Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis. In Neurobiology of aging, 74, 235.e9-235.e12. doi:10.1016/j.neurobiolaging.2018.09.020. https://pubmed.ncbi.nlm.nih.gov/30337194/
4. Nahm, Minyeop, Lim, Su Min, Kim, Young-Eun, Ki, Chang-Seok, Kim, Seung Hyun. . ANXA11 mutations in ALS cause dysregulation of calcium homeostasis and stress granule dynamics. In Science translational medicine, 12, . doi:10.1126/scitranslmed.aax3993. https://pubmed.ncbi.nlm.nih.gov/33087501/
5. Snyder, Allison, Ryan, Veronica H, Hawrot, James, Cookson, Mark R, Ward, Michael E. 2023. An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndrome. In Research square, , . doi:10.21203/rs.3.rs-3462973/v1. https://pubmed.ncbi.nlm.nih.gov/37886540/