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2. Aishwarya, Richa, Abdullah, Chowdhury S, Morshed, Mahboob, Remex, Naznin Sultana, Bhuiyan, Md Shenuarin. 2021. Sigmar1's Molecular, Cellular, and Biological Functions in Regulating Cellular Pathophysiology. In Frontiers in physiology, 12, 705575. doi:10.3389/fphys.2021.705575. https://pubmed.ncbi.nlm.nih.gov/34305655/
3. Che, Xiang-Qian, Lin, Guo-Zhen, Liu, Xiao-Hong, Zhao, Qian-Hua, Ren, Ru-Jing. . Genetic and Neuroimaging Analysis of SIGMAR1 for Frontotemporal Dementia. In Journal of Alzheimer's disease : JAD, 95, 469-475. doi:10.3233/JAD-221195. https://pubmed.ncbi.nlm.nih.gov/37545231/
4. Ohi, Kazutaka, Hashimoto, Ryota, Yasuda, Yuka, Kasai, Kiyoto, Takeda, Masatoshi. 2011. The SIGMAR1 gene is associated with a risk of schizophrenia and activation of the prefrontal cortex. In Progress in neuro-psychopharmacology & biological psychiatry, 35, 1309-15. doi:10.1016/j.pnpbp.2011.04.008. https://pubmed.ncbi.nlm.nih.gov/21549171/
5. Chen, Yu-Jie, Knupp, Jeffrey, Wang, Emily, Arvan, Peter, Tsai, Billy. 2024. SIGMAR1/Sigma-1 receptor: a key regulator in stabilizing and translating LC3B mRNA for autophagosome formation. In Autophagy, 20, 2843-2845. doi:10.1080/15548627.2024.2413313. https://pubmed.ncbi.nlm.nih.gov/39369298/
6. Ganassi, Massimo, Zammit, Peter S. 2022. Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies. In European journal of translational myology, 32, . doi:10.4081/ejtm.2022.10064. https://pubmed.ncbi.nlm.nih.gov/35302338/
7. Horga, Alejandro, Tomaselli, Pedro J, Gonzalez, Michael A, Züchner, Stephan, Reilly, Mary M. 2016. SIGMAR1 mutation associated with autosomal recessive Silver-like syndrome. In Neurology, 87, 1607-1612. doi:. https://pubmed.ncbi.nlm.nih.gov/27629094/
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