1. Wang, Huiqing, Dou, Shanshan, Wang, Chunmei, Cheng, Baohua, Yan, Fuling. 2023. Identification and Experimental Validation of Parkinson's Disease with Major Depressive Disorder Common Genes. In Molecular neurobiology, 60, 6092-6108. doi:10.1007/s12035-023-03451-3. https://pubmed.ncbi.nlm.nih.gov/37418066/
2. Leclercq, Bastien, Weiner, Allon, Zola, Marta, Zhao, Min, Behar-Cohen, Francine. 2023. The choroidal nervous system: a link between mineralocorticoid receptor and pachychoroid. In Acta neuropathologica, 146, 747-766. doi:10.1007/s00401-023-02628-3. https://pubmed.ncbi.nlm.nih.gov/37682293/
3. Barzasi, Marta, Spinola, Alessio, Costa, Alex, DiLuca, Monica, Gardoni, Fabrizio. 2025. Arg209Lys and Gln508His missense variants in Rabphilin 3A cause pre- and post-synaptic dysfunctions at excitatory glutamatergic synapses. In Scientific reports, 15, 8698. doi:10.1038/s41598-025-93403-9. https://pubmed.ncbi.nlm.nih.gov/40082528/
4. Maselli, Ricardo A, Vázquez, Jessica, Schrumpf, Leah, Wollmann, Robert L, Ferns, Michael. 2018. Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A. In Molecular genetics & genomic medicine, 6, 434-440. doi:10.1002/mgg3.370. https://pubmed.ncbi.nlm.nih.gov/29441694/
5. Yang, Ming-Chun, Wu, Di, Sun, Hui, Wang, Lian-Kun, Chen, Xiao-Feng. 2022. A Metabolic Plasticity-Based Signature for Molecular Classification and Prognosis of Lower-Grade Glioma. In Brain sciences, 12, . doi:10.3390/brainsci12091138. https://pubmed.ncbi.nlm.nih.gov/36138874/
智鼠故事 
