1. Chiereghin, Chiara, Robusto, Michela, Mauri, Lucia, Asselta, Rosanna, Soldà, Giulia. 2021. SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa. In Frontiers in genetics, 12, 606630. doi:10.3389/fgene.2021.606630. https://pubmed.ncbi.nlm.nih.gov/33643381/
2. Ren, Tian-li, Han, Zhi-jun, Yang, Cheng-jian, Ji, Xiao-Jing, Zhou, Fan-fan. 2014. Association of SLC22A4 gene polymorphism with Rheumatoid arthritis in the Chinese population. In Journal of biochemical and molecular toxicology, 28, 206-10. doi:10.1002/jbt.21554. https://pubmed.ncbi.nlm.nih.gov/24599653/
3. Lu, Dading, Cai, Heng, Li, Yugang, Xiao, Xiong, Li, Zhiqing. 2023. Investigating the ID3/SLC22A4 as immune-related signatures in ischemic stroke. In Aging, 15, 14803-14829. doi:10.18632/aging.205308. https://pubmed.ncbi.nlm.nih.gov/38112574/
4. Feng, Yun, Zheng, Ping, Zhao, Hang, Wu, Kai. . SLC22A4 and SLC22A5 gene polymorphisms and Crohn's disease in the Chinese Han population. In Journal of digestive diseases, 10, 181-7. doi:10.1111/j.1751-2980.2009.00383.x. https://pubmed.ncbi.nlm.nih.gov/19659785/
5. Yamada, Ryo, Tokuhiro, Shinya, Chang, Xiotian, Yamamoto, Kazuhiko. 2004. SLC22A4 and RUNX1: identification of RA susceptible genes. In Journal of molecular medicine (Berlin, Germany), 82, 558-64. doi:. https://pubmed.ncbi.nlm.nih.gov/15184985/
6. Yang, Lun-Zhe, Yang, Yong, Hong, Chuan, Liu, Yi-Lin, Chen, Guang-Zhong. 2024. Systematic Mendelian Randomization Exploring Druggable Genes for Hemorrhagic Strokes. In Molecular neurobiology, 62, 1359-1372. doi:10.1007/s12035-024-04336-9. https://pubmed.ncbi.nlm.nih.gov/38977622/