1. Allach El Khattabi, Laïla, Heide, Solveig, Caberg, Jean-Hubert, Benzacken, Brigitte, Pipiras, Eva. 2018. 16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlations. In Journal of medical genetics, 57, 301-307. doi:10.1136/jmedgenet-2018-105389. https://pubmed.ncbi.nlm.nih.gov/30287593/
2. Chomiak, Alison A, Guo, Yan, Kopsidas, Caroline A, Doughty, Martin L, Feng, Yuanyi. 2022. Nde1 is required for heterochromatin compaction and stability in neocortical neurons. In iScience, 25, 104354. doi:10.1016/j.isci.2022.104354. https://pubmed.ncbi.nlm.nih.gov/35601919/
3. Soto-Perez, Jaseph, Baumgartner, Marybeth, Kanadia, Rahul N. 2020. Role of NDE1 in the Development and Evolution of the Gyrified Cortex. In Frontiers in neuroscience, 14, 617513. doi:10.3389/fnins.2020.617513. https://pubmed.ncbi.nlm.nih.gov/33390896/
4. Bradshaw, Nicholas J, Ukkola-Vuoti, Liisa, Pankakoski, Maiju, Haukka, Jari, Hennah, William. . The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to microRNA-484. In Open biology, 7, . doi:10.1098/rsob.170153. https://pubmed.ncbi.nlm.nih.gov/29142105/
5. Tan, Li, Bi, Bo, Zhao, Peiwei, Shao, Jianbo, He, Xuelian. 2017. Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review. In BMC medical genetics, 18, 141. doi:10.1186/s12881-017-0501-9. https://pubmed.ncbi.nlm.nih.gov/29191162/
6. Bradshaw, Nicholas J, Hayashi, Mirian A F. 2016. NDE1 and NDEL1 from genes to (mal)functions: parallel but distinct roles impacting on neurodevelopmental disorders and psychiatric illness. In Cellular and molecular life sciences : CMLS, 74, 1191-1210. doi:10.1007/s00018-016-2395-7. https://pubmed.ncbi.nlm.nih.gov/27742926/