1. Teunissen, Mariel W A, Kamsteeg, Erik-Jan, Sallevelt, Suzanne C E H, Vermeulen, R Jeroen, Nicolai, Joost. 2021. Biallelic Variants in the COLGALT1 Gene Causes Severe Congenital Porencephaly: A Case Report. In Neurology. Genetics, 7, e564. doi:10.1212/NXG.0000000000000564. https://pubmed.ncbi.nlm.nih.gov/33709034/
2. Miyatake, Satoko, Schneeberger, Sacha, Koyama, Norihisa, Hennet, Thierry, Matsumoto, Naomichi. 2018. Biallelic COLGALT1 variants are associated with cerebral small vessel disease. In Annals of neurology, 84, 843-853. doi:10.1002/ana.25367. https://pubmed.ncbi.nlm.nih.gov/30412317/
3. Geister, Krista A, Lopez-Jimenez, Alberto Jose, Houghtaling, Scott, Vanacore, Roberto, Beier, David R. 2019. Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects. In Disease models & mechanisms, 12, . doi:10.1242/dmm.037176. https://pubmed.ncbi.nlm.nih.gov/31101663/
4. Brazier, Jon, Antrobus, Mark R, Herbert, Adam J, Pitsiladis, Yannis P, Williams, Alun G. 2022. Gene variants previously associated with reduced soft tissue injury risk: Part 1 - independent associations with elite status in rugby. In European journal of sport science, 23, 726-735. doi:10.1080/17461391.2022.2053752. https://pubmed.ncbi.nlm.nih.gov/35293840/
5. Ai, Xiaoshun, Shen, Hong, Wang, Yangyanqiu, Niu, Furong, Zhou, Qing. 2022. Developing a Diagnostic Model to Predict the Risk of Asthma Based on Ten Macrophage-Related Gene Signatures. In BioMed research international, 2022, 3439010. doi:10.1155/2022/3439010. https://pubmed.ncbi.nlm.nih.gov/36467876/
6. Fan, Wei, Chen, Xiaoyun, Li, Ruiping, Wang, Yunyun, Guo, Yuzhen. 2022. A prognostic risk model for ovarian cancer based on gene expression profiles from gene expression omnibus database. In Biochemical genetics, 61, 138-150. doi:10.1007/s10528-022-10232-5. https://pubmed.ncbi.nlm.nih.gov/35761155/
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