1. Kose, Engin, Besci, Ozge, Gudeloglu, Elif, Ozen, Selime, Isguder, Rana. . Transcobalamin II deficiency in twins with a novel variant in the TCN2 gene: case report and review of literature. In Journal of pediatric endocrinology & metabolism : JPEM, 33, 1487-1499. doi:10.1515/jpem-2020-0096. https://pubmed.ncbi.nlm.nih.gov/32841161/
2. Sun, Hong, Li, Ling, Yan, Jingchao, Huang, Taomin. 2024. Prioritization of drug targets for thyroid cancer: a multi-omics Mendelian randomization study. In Endocrine, 86, 732-743. doi:10.1007/s12020-024-03933-x. https://pubmed.ncbi.nlm.nih.gov/38896366/
3. Ge, Yi-Jun, Chen, Shi-Dong, Wu, Bang-Sheng, Jia, Jian-Ping, Yu, Jin-Tai. 2024. Genome-wide meta-analysis identifies ancestry-specific loci for Alzheimer's disease. In Alzheimer's & dementia : the journal of the Alzheimer's Association, 20, 6243-6256. doi:10.1002/alz.14121. https://pubmed.ncbi.nlm.nih.gov/39023044/
4. Grarup, Niels, Sulem, Patrick, Sandholt, Camilla H, Stefánsson, Kari, Pedersen, Oluf. 2013. Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. In PLoS genetics, 9, e1003530. doi:10.1371/journal.pgen.1003530. https://pubmed.ncbi.nlm.nih.gov/23754956/
5. Lanktree, Matthew B, Perrot, Nicolas, Smyth, Andrew, Yusuf, Salim, Paré, Guillaume. 2023. A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulation. In Kidney international, 104, 1170-1184. doi:10.1016/j.kint.2023.08.025. https://pubmed.ncbi.nlm.nih.gov/37774922/
6. Luo, Juan, Guo, Hongxi, Feng, Lifang, Yao, Hui, Chen, Xiaohong. 2022. Case report: Novel compound-heterozygous mutations in the TCN2 gene identified in a chinese girl with transcobalamin deficiency. In Frontiers in genetics, 13, 951007. doi:10.3389/fgene.2022.951007. https://pubmed.ncbi.nlm.nih.gov/36035190/
7. Liu, Shan, Liu, Mengwei, Li, Qian, Nie, Fangfang, Liu, Wanyang. . Association of single nucleotide polymorphisms of MTHFR, TCN2, RNF213 with susceptibility to hypertension and blood pressure. In Bioscience reports, 39, . doi:10.1042/BSR20191454. https://pubmed.ncbi.nlm.nih.gov/31815282/
8. Zhan, Shihong, Cheng, Fangfang, He, Hailong, Hu, Shaoyan, Feng, Xing. 2020. Identification of transcobalamin deficiency with two novel mutations in the TCN2 gene in a Chinese girl with abnormal immunity: a case report. In BMC pediatrics, 20, 460. doi:10.1186/s12887-020-02357-6. https://pubmed.ncbi.nlm.nih.gov/33023511/
智鼠故事 
