1. Su, Jun, Li, Yue, Liu, Qing, Qin, Chaoying, Li, Yang. 2022. Identification of SSBP1 as a ferroptosis-related biomarker of glioblastoma based on a novel mitochondria-related gene risk model and in vitro experiments. In Journal of translational medicine, 20, 440. doi:10.1186/s12967-022-03657-4. https://pubmed.ncbi.nlm.nih.gov/36180956/
2. Piro-Mégy, Camille, Sarzi, Emmanuelle, Tarrés-Solé, Aleix, Sola, Maria, Delettre, Cécile. . Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy. In The Journal of clinical investigation, 130, 143-156. doi:10.1172/JCI128513. https://pubmed.ncbi.nlm.nih.gov/31550237/
3. Li, Qiuchen, Qu, Falin, Li, Renli, Chen, Weigang, Zheng, Yong. 2017. A functional polymorphism of SSBP1 gene predicts prognosis and response to chemotherapy in resected gastric cancer patients. In Oncotarget, 8, 110861-110876. doi:10.18632/oncotarget.22864. https://pubmed.ncbi.nlm.nih.gov/29340022/
4. Zelinger, Lina, Swaroop, Anand. . SSBP1 faux pas in mitonuclear tango causes optic neuropathy. In The Journal of clinical investigation, 130, 62-64. doi:10.1172/JCI132532. https://pubmed.ncbi.nlm.nih.gov/31738184/
5. Huang, Jian, Xie, Zheng-Fu. . Identification of SSBP1 as a prognostic marker in human lung adenocarcinoma using bioinformatics approaches. In Mathematical biosciences and engineering : MBE, 19, 3022-3035. doi:10.3934/mbe.2022139. https://pubmed.ncbi.nlm.nih.gov/35240818/
6. Jurkute, Neringa, Leu, Costin, Pogoda, Hans-Martin, Yu-Wai-Man, Patrick, Votruba, Marcela. 2019. SSBP1 mutations in dominant optic atrophy with variable retinal degeneration. In Annals of neurology, 86, 368-383. doi:10.1002/ana.25550. https://pubmed.ncbi.nlm.nih.gov/31298765/