1. Jacher, Joseph E, Innis, Jeffrey W. 2018. Interstitial microdeletion of the 1p34.3p34.2 region. In Molecular genetics & genomic medicine, 6, 673-7. doi:10.1002/mgg3.409. https://pubmed.ncbi.nlm.nih.gov/29726122/
2. Kumar, Ravinesh A, Sudi, Jyotsna, Babatz, Timothy D, Christian, Susan L, Dobyns, William B. 2009. A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. In Journal of medical genetics, 47, 81-90. doi:10.1136/jmg.2008.065821. https://pubmed.ncbi.nlm.nih.gov/19546099/
3. Tang, Jiezhang, Wu, Xuechen, Cheng, Bo, Lu, Yajie. 2023. Identification of a polyamine-related signature and six novel prognostic biomarkers in oral squamous cell carcinoma. In Frontiers in molecular biosciences, 10, 1073770. doi:10.3389/fmolb.2023.1073770. https://pubmed.ncbi.nlm.nih.gov/36733434/
4. Deng, Heng, Chen, Shuo, Yuan, Xiancang, Zhang, Jun. 2022. Transcriptome Sequencing Analysis of the Effect of β-Elemene on Colorectal Cancer from the lncRNA-miRNA-mRNA Perspective. In Genetics research, 2022, 5896296. doi:10.1155/2022/5896296. https://pubmed.ncbi.nlm.nih.gov/36160034/
5. Weidenhofer, Judith, Scott, Rodney J, Tooney, Paul A. 2008. Investigation of the expression of genes affecting cytomatrix active zone function in the amygdala in schizophrenia: effects of antipsychotic drugs. In Journal of psychiatric research, 43, 282-90. doi:10.1016/j.jpsychires.2008.04.001. https://pubmed.ncbi.nlm.nih.gov/18490030/
6. Chandrasekaran, Sreedevi, Bonchev, Danail. 2013. A network view on Parkinson's disease. In Computational and structural biotechnology journal, 7, e201304004. doi:10.5936/csbj.201304004. https://pubmed.ncbi.nlm.nih.gov/24688734/
7. Stielow, Bastian, Krüger, Imme, Diezko, Rolf, Philipsen, Sjaak, Suske, Guntram. 2010. Epigenetic silencing of spermatocyte-specific and neuronal genes by SUMO modification of the transcription factor Sp3. In PLoS genetics, 6, e1001203. doi:10.1371/journal.pgen.1001203. https://pubmed.ncbi.nlm.nih.gov/21085687/
8. Huang, Xiu-Feng, Mao, Jian-Yang, Huang, Zhi-Qin, Wang, Qing-Feng, Jin, Zi-Bing. . Genome-Wide Detection of Copy Number Variations in Unsolved Inherited Retinal Disease. In Investigative ophthalmology & visual science, 58, 424-429. doi:10.1167/iovs.16-20705. https://pubmed.ncbi.nlm.nih.gov/28118666/
智鼠故事 
