1. Grasberger, Helmut, Magis, Andrew T, Sheng, Elisa, Omenn, Gilbert S, Kao, John Y. . DUOX2 variants associate with preclinical disturbances in microbiota-immune homeostasis and increased inflammatory bowel disease risk. In The Journal of clinical investigation, 131, . doi:10.1172/JCI141676. https://pubmed.ncbi.nlm.nih.gov/33651715/
2. Wang, Fengqi, Zang, Yucui, Li, Miaomiao, Wang, Fang, Liu, Shiguo. 2020. DUOX2 and DUOXA2 Variants Confer Susceptibility to Thyroid Dysgenesis and Gland-in-situ With Congenital Hypothyroidism. In Frontiers in endocrinology, 11, 237. doi:10.3389/fendo.2020.00237. https://pubmed.ncbi.nlm.nih.gov/32425884/
3. Kostopoulou, Eirini, Miliordos, Konstantinos, Spiliotis, Bessie. 2021. Genetics of primary congenital hypothyroidism-a review. In Hormones (Athens, Greece), 20, 225-236. doi:10.1007/s42000-020-00267-x. https://pubmed.ncbi.nlm.nih.gov/33400193/
4. Vermot, Annelise, Petit-Härtlein, Isabelle, Smith, Susan M E, Fieschi, Franck. 2021. NADPH Oxidases (NOX): An Overview from Discovery, Molecular Mechanisms to Physiology and Pathology. In Antioxidants (Basel, Switzerland), 10, . doi:10.3390/antiox10060890. https://pubmed.ncbi.nlm.nih.gov/34205998/
5. Yang, Yuanming, Hua, Yiwei, Zheng, Huan, Qin, Shumin, Huang, Shaogang. 2023. Biomarkers prediction and immune landscape in ulcerative colitis: Findings based on bioinformatics and machine learning. In Computers in biology and medicine, 168, 107778. doi:10.1016/j.compbiomed.2023.107778. https://pubmed.ncbi.nlm.nih.gov/38070204/
6. Long, Wei, Guo, Fang, Yao, Ruen, Yu, Bin, Xue, Peng. 2021. Genetic and Phenotypic Characteristics of Congenital Hypothyroidism in a Chinese Cohort. In Frontiers in endocrinology, 12, 705773. doi:10.3389/fendo.2021.705773. https://pubmed.ncbi.nlm.nih.gov/34539567/
7. Zhou, Duo, Yang, Rulai, Huang, Xinwen, Yang, Jianbin, Zhao, Zhengyan. 2023. Results of neonatal screening for congenital hypothyroidism and hyperphenylalaninemia in Zhejiang province from 1999 to 2022. In Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 52, 683-692. doi:10.3724/zdxbyxb-2023-0473. https://pubmed.ncbi.nlm.nih.gov/38105685/
8. Kyodo, Reiko, Takeuchi, Ichiro, Narumi, Satoshi, Shimizu, Toshiaki, Arai, Katsuhiro. 2022. Novel biallelic mutations in the DUOX2 gene underlying very early-onset inflammatory bowel disease: A case report. In Clinical immunology (Orlando, Fla.), 238, 109015. doi:10.1016/j.clim.2022.109015. https://pubmed.ncbi.nlm.nih.gov/35429653/
9. Chen, Xi, Kong, Xiaohong, Zhu, Jie, Ding, Guifeng, Wang, Huijuan. 2018. Mutational Spectrum Analysis of Seven Genes Associated with Thyroid Dyshormonogenesis. In International journal of endocrinology, 2018, 8986475. doi:10.1155/2018/8986475. https://pubmed.ncbi.nlm.nih.gov/30154845/