1. Sasaki, Hidenao, Emi, Mitsuru, Iijima, Hiroshi, Utsumi, Jun, Matsubara, Kenichi. 2011. Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy. In Molecular brain, 4, 24. doi:10.1186/1756-6606-4-24. https://pubmed.ncbi.nlm.nih.gov/21658278/
2. Wang, Xuejiao, Yang, Guang, Li, Jun, Meng, Chao, Xue, Zengming. 2024. Dynamic molecular signatures of acute myocardial infarction based on transcriptomics and metabolomics. In Scientific reports, 14, 10175. doi:10.1038/s41598-024-60945-3. https://pubmed.ncbi.nlm.nih.gov/38702356/
3. Ferician, Adela Maria, Ferician, Ovidiu Catalin, Cumpanas, Andrei Dragos, Barmayoun, Ariana, Cimpean, Anca Maria. . Heterogeneity of Platelet Derived Growth Factor Pathway Gene Expression Profile Defines Three Distinct Subgroups of Renal Cell Carcinomas. In Cancer genomics & proteomics, 19, 477-489. doi:10.21873/cgp.20334. https://pubmed.ncbi.nlm.nih.gov/35732321/
4. Cardenas, Ryan, Prinsley, Peter, Philpott, Carl, Brewer, Daniel S, Jennings, Barbara A. 2023. Whole exome sequencing study identifies candidate loss of function variants and locus heterogeneity in familial cholesteatoma. In PloS one, 18, e0272174. doi:10.1371/journal.pone.0272174. https://pubmed.ncbi.nlm.nih.gov/36920900/