1. Harrison, Paul J, Bannerman, David M. 2023. GRIN2A (NR2A): a gene contributing to glutamatergic involvement in schizophrenia. In Molecular psychiatry, 28, 3568-3572. doi:10.1038/s41380-023-02265-y. https://pubmed.ncbi.nlm.nih.gov/37736757/
2. Symonds, Joseph D, Zuberi, Sameer M, Johnson, Michael R. . Advances in epilepsy gene discovery and implications for epilepsy diagnosis and treatment. In Current opinion in neurology, 30, 193-199. doi:10.1097/WCO.0000000000000433. https://pubmed.ncbi.nlm.nih.gov/28212175/
3. Trubetskoy, Vassily, Pardiñas, Antonio F, Qi, Ting, Walters, James T R, O'Donovan, Michael C. 2022. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. In Nature, 604, 502-508. doi:10.1038/s41586-022-04434-5. https://pubmed.ncbi.nlm.nih.gov/35396580/
4. Farsi, Zohreh, Nicolella, Ally, Simmons, Sean K, Levin, Joshua Z, Sheng, Morgan. 2023. Brain-region-specific changes in neurons and glia and dysregulation of dopamine signaling in Grin2a mutant mice. In Neuron, 111, 3378-3396.e9. doi:10.1016/j.neuron.2023.08.004. https://pubmed.ncbi.nlm.nih.gov/37657442/
5. Turner, Samantha J, Mayes, Angela K, Verhoeven, Andrea, Morgan, Angela T, Scheffer, Ingrid E. 2015. GRIN2A: an aptly named gene for speech dysfunction. In Neurology, 84, 586-93. doi:10.1212/WNL.0000000000001228. https://pubmed.ncbi.nlm.nih.gov/25596506/
6. Luo, Xian, Yang, Kaiming, Jiang, Meiling, Lai, Liangxue, Zou, Qingjian. 2023. Generation of a homozygous GRIN2A gene knockout human embryonic stem cell line using CRISPR/Cas9 system. In Stem cell research, 69, 103121. doi:10.1016/j.scr.2023.103121. https://pubmed.ncbi.nlm.nih.gov/37182381/
7. Bobbili, Dheeraj R, Lal, Dennis, May, Patrick, Lerche, Holger, Neubauer, Bernd A. 2018. Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. In European journal of human genetics : EJHG, 26, 258-264. doi:10.1038/s41431-017-0034-x. https://pubmed.ncbi.nlm.nih.gov/29358611/