Hongjie Yuan
Affiliations: | Pharmacology | Rollins Research Center, Emory University |
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| Montanucci L, Brünger T, Bhattarai N, et al. (2024) Distances from ligands as main predictive features for pathogenicity and functional effect of variants in NMDA receptors. Medrxiv : the Preprint Server For Health Sciences |
| Xu Y, Song R, Perszyk RE, et al. (2024) De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor. Cellular and Molecular Life Sciences : Cmls. 81: 153 |
| Allen JP, Garber KB, Perszyk R, et al. (2023) Clinical features, functional consequences, and rescue pharmacology of missense GRID1 and GRID2 human variants. Human Molecular Genetics |
| XiangWei W, Perszyk RE, Liu N, et al. (2023) Clinical and functional consequences of GRIA variants in patients with neurological diseases. Cellular and Molecular Life Sciences : Cmls. 80: 345 |
| Camp CR, Vlachos A, Klöckner C, et al. (2023) Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons. Communications Biology. 6: 952 |
| Song R, Zhang J, Perszyk RE, et al. (2023) Differential responses of disease-related GRIN variants located in pore-forming M2 domain of N-methyl-D-aspartate receptor to FDA-approved inhibitors. Journal of Neurochemistry |
| Liu N, Li J, Gao K, et al. (2023) De novo CLPTM1 variants with reduced GABA R current response in patients with epilepsy. Epilepsia |
| D'Erasmo MP, Akins NS, Ma P, et al. (2023) Development of a Dihydroquinoline-Pyrazoline GluN2C/2D-Selective Negative Allosteric Modulator of the -Methyl-d-aspartate Receptor. Acs Chemical Neuroscience |
| Hanson JE, Yuan H, Perszyk RE, et al. (2023) Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology |
| Myers SJ, Yuan H, Perszyk RE, et al. (2023) Classification of missense variants in the N-methyl-D-aspartate receptor GRIN gene family as gain- or loss-of-function. Human Molecular Genetics |