1. Lyon, Gholson J, Vedaie, Marall, Beisheim, Travis, Marmorstein, Ronen, Herr-Israel, Ellen. 2023. Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome. In European journal of human genetics : EJHG, 31, 824-833. doi:10.1038/s41431-023-01368-y. https://pubmed.ncbi.nlm.nih.gov/37130971/
2. Yubero, Delia, Martorell, Loreto, Nunes, Tania, Lyon, Gholson J, Ortigoza-Escobar, Juan Darío. 2022. Neurodevelopmental Gene-Related Dystonia: A Pediatric Case with NAA15 Variant. In Movement disorders : official journal of the Movement Disorder Society, 37, 2320-2321. doi:10.1002/mds.29241. https://pubmed.ncbi.nlm.nih.gov/36221186/
3. Cheng, Hanyin, Dharmadhikari, Avinash V, Varland, Sylvia, Meng, Linyan, Lyon, Gholson J. 2018. Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. In American journal of human genetics, 102, 985-994. doi:10.1016/j.ajhg.2018.03.004. https://pubmed.ncbi.nlm.nih.gov/29656860/
4. Tian, Yu, Xie, Hua, Yang, Shenghai, Chen, Xiaoli, Wang, Lin. 2022. Possible Catch-Up Developmental Trajectories for Children with Mild Developmental Delay Caused by NAA15 Pathogenic Variants. In Genes, 13, . doi:10.3390/genes13030536. https://pubmed.ncbi.nlm.nih.gov/35328089/