1. Suri, Fatemeh, Yazdani, Shahin, Chapi, Marjan, Turk, Casey, Elahi, Elahe. . COL18A1 is a candidate eye iridocorneal angle-closure gene in humans. In Human molecular genetics, 27, 3772-3786. doi:10.1093/hmg/ddy256. https://pubmed.ncbi.nlm.nih.gov/30007336/
2. Zhang, Sheng, Xie, Yuanlong, Yan, Feifei, Cai, Lin, Deng, Zhouming. 2021. Negative pressure wound therapy improves bone regeneration by promoting osteogenic differentiation via the AMPK-ULK1-autophagy axis. In Autophagy, 18, 2229-2245. doi:10.1080/15548627.2021.2016231. https://pubmed.ncbi.nlm.nih.gov/34964701/
3. Jiang, Zixuan, Sun, Wenmin, Zhang, Qingjiong, Wang, Panfeng. 2023. Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1. In Stem cell research, 70, 103131. doi:10.1016/j.scr.2023.103131. https://pubmed.ncbi.nlm.nih.gov/37269665/
4. Irene Díez García-Prieto, I, Lopez-Martín, Sara, Albert, Jacobo, Izzi, Valerio, Fernández-Jaén, Alberto. 2022. Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findings. In Neurocase, 28, 11-18. doi:10.1080/13554794.2021.1928228. https://pubmed.ncbi.nlm.nih.gov/35253627/