1. Cerdán-Vélez, Daniel, Tress, Michael Liam. 2024. The T2T-CHM13 reference assembly uncovers essential WASH1 and GPRIN2 paralogues. In Bioinformatics advances, 4, vbae029. doi:10.1093/bioadv/vbae029. https://pubmed.ncbi.nlm.nih.gov/38464973/
2. Liu, Ming, Wu, Shaoxian, Wu, Haoyu, Zhu, Dawei, Jiang, Jingting. 2024. Ferredoxin 1: a gatekeeper in halting lung adenocarcinoma progression through activation of the GPRIN2 signaling pathway. In Journal of translational medicine, 22, 510. doi:10.1186/s12967-024-05277-6. https://pubmed.ncbi.nlm.nih.gov/38802900/
3. Khalilipour, Narjes, Baranova, Ancha, Jebelli, Amir, Bruskin, Sergey, Abbaszadegan, Mohammad Reza. 2017. Familial Esophageal Squamous Cell Carcinoma with damaging rare/germline mutations in KCNJ12/KCNJ18 and GPRIN2 genes. In Cancer genetics, 221, 46-52. doi:10.1016/j.cancergen.2017.11.011. https://pubmed.ncbi.nlm.nih.gov/29405996/
4. Qiu, Xue, Lin, Jinyan, Chen, Yanbing, Liang, Bixiao, Li, Lang. 2021. Identification of Hub Genes Associated with Abnormal Endothelial Function in Early Coronary Atherosclerosis. In Biochemical genetics, 60, 1189-1204. doi:10.1007/s10528-021-10139-7. https://pubmed.ncbi.nlm.nih.gov/34800203/
5. Crisafulli, Concetta, Chiesa, Alberto, Han, Changsu, Pae, Chi-Un, Serretti, Alessandro. 2011. Case-control association study for 10 genes in patients with schizophrenia: influence of 5HTR1A variation rs10042486 on schizophrenia and response to antipsychotics. In European archives of psychiatry and clinical neuroscience, 262, 199-205. doi:10.1007/s00406-011-0278-3. https://pubmed.ncbi.nlm.nih.gov/22120873/
6. Lee, Ning Yuan, Hum, Melissa, Amali, Aseervatham Anusha, Lee, Soo-Chin, Lee, Ann S G. 2022. Whole-exome sequencing of BRCA-negative breast cancer patients and case-control analyses identify variants associated with breast cancer susceptibility. In Human genomics, 16, 61. doi:10.1186/s40246-022-00435-7. https://pubmed.ncbi.nlm.nih.gov/36424660/