1. Sirokha, Dmytro, Rayevsky, Alexey, Gorodna, Olexandra, Kusz-Zamelczyk, Kamila, Livshits, Ludmila. 2024. Mutations in STARD8 (DLC3) May Cause 46,XY Gonadal Dysgenesis. In Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation, 17, 181-189. doi:10.1159/000537877. https://pubmed.ncbi.nlm.nih.gov/38447543/
2. Mo, Ha Yoon, Moon, Seong Won, An, Chang Hyeok, Lee, Sug Hyung. 2023. Regional bias of tumor suppressor gene mutations of STARD8 and WNK2 in colon cancers. In Pathology, research and practice, 253, 155000. doi:10.1016/j.prp.2023.155000. https://pubmed.ncbi.nlm.nih.gov/38091885/
3. Zhang, Shuanglong, Chang, Xiaojing, Ma, Jinguo, Li, Zhenhua, Dai, Dongqiu. 2018. Downregulation of STARD8 in gastric cancer and its involvement in gastric cancer progression. In OncoTargets and therapy, 11, 2955-2961. doi:10.2147/OTT.S154524. https://pubmed.ncbi.nlm.nih.gov/29849465/
4. Błoch, Michal, Gasperowicz, Piotr, Gerus, Sylwester, Karpiński, Pawel, Śmigiel, Robert. 2023. Epigenetic Findings in Twins with Esophageal Atresia. In Genes, 14, . doi:10.3390/genes14091822. https://pubmed.ncbi.nlm.nih.gov/37761962/
5. Li, Jun, Zong, Suyu, Wan, Yang, Zhang, Yingchi, Zhu, Xiaofan. 2023. Integration of Transcriptomic Features to Improve Prognosis Prediction of Pediatric Acute Myeloid Leukemia With KMT2A Rearrangement. In HemaSphere, 7, e979. doi:10.1097/HS9.0000000000000979. https://pubmed.ncbi.nlm.nih.gov/38026790/
6. Xu, Liyan, Yang, Kaili, Zhu, Meng, Pang, Chenjiu, Ren, Shengwei. 2022. Trio-based exome sequencing broaden the genetic spectrum in keratoconus. In Experimental eye research, 226, 109342. doi:10.1016/j.exer.2022.109342. https://pubmed.ncbi.nlm.nih.gov/36502923/