1. Guo, Hui, Bettella, Elisa, Marcogliese, Paul C, Murgia, Alessandra, Eichler, Evan E. 2019. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. In Nature communications, 10, 4679. doi:10.1038/s41467-019-12435-8. https://pubmed.ncbi.nlm.nih.gov/31616000/
2. Huang, Kai, Wu, Hao, Xu, Xiangyang, Li, Qin, Han, Lin. 2023. Identification of TGF-β-related genes in cardiac hypertrophy and heart failure based on single cell RNA sequencing. In Aging, 15, 7187-7218. doi:10.18632/aging.204901. https://pubmed.ncbi.nlm.nih.gov/37498303/
3. Tassano, E, Accogli, A, Ronchetto, P, Malacarne, M, Coviello, D A. 2020. 17q23.3 de novo microdeletion involving only TANC2 gene: A new case. In European journal of medical genetics, 63, 104094. doi:10.1016/j.ejmg.2020.104094. https://pubmed.ncbi.nlm.nih.gov/33160097/
4. Chu, Manman, Xu, Dan, Xie, Jiayang, Wang, Junling, Jia, Tianming. . [Clinical and genetic analysis of two children with TANC2 gene variants and a literature review]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 41, 1195-1200. doi:10.3760/cma.j.cn511374-20240313-00171. https://pubmed.ncbi.nlm.nih.gov/39344613/
5. Long, Fei, Zheng, Jing, Zhou, Jiayi, Hu, Ping, Xiong, Bo. 2022. Knockout of tanc2 causes autism-like behavior and sleep disturbance in zebrafish. In Autism research : official journal of the International Society for Autism Research, 16, 524-534. doi:10.1002/aur.2880. https://pubmed.ncbi.nlm.nih.gov/36534563/
6. Garrett, Lillian, Da Silva-Buttkus, Patricia, Rathkolb, Birgit, Hölter, Sabine M, Hrabě de Angelis, Martin. 2022. Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk. In Disease models & mechanisms, 15, . doi:10.1242/dmm.049205. https://pubmed.ncbi.nlm.nih.gov/34964047/
7. Tian, Yang, Shi, Zhen, Hou, Chi, Li, Xiaojing, Chen, Wen-Xiong. 2021. Truncating mutation in TANC2 in a Chinese boy associated with Lennox-Gastaut syndrome: a case report. In BMC pediatrics, 21, 546. doi:10.1186/s12887-021-03021-3. https://pubmed.ncbi.nlm.nih.gov/34861844/
8. Li, Xueqian, Qi, Jiaqian, Song, Xiaofei, Yang, Jingyi, Han, Yue. 2022. DLC1 deficiency at diagnosis predicts poor prognosis in acute myeloid leukemia. In Experimental hematology & oncology, 11, 74. doi:10.1186/s40164-022-00335-5. https://pubmed.ncbi.nlm.nih.gov/36258263/
9. Mahmood, Sardar Faisal, Gruel, Nadège, Chapeaublanc, Elodie, Radvanyi, François, Bernard-Pierrot, Isabelle. 2013. A siRNA screen identifies RAD21, EIF3H, CHRAC1 and TANC2 as driver genes within the 8q23, 8q24.3 and 17q23 amplicons in breast cancer with effects on cell growth, survival and transformation. In Carcinogenesis, 35, 670-82. doi:10.1093/carcin/bgt351. https://pubmed.ncbi.nlm.nih.gov/24148822/