1. Kazeminasab, Somayeh, Taskiran, Ibrahim Ihsan, Fattahi, Zohreh, Najmabadi, Hossein, Kahrizi, Kimia. 2018. CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. In American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 177, 691-699. doi:10.1002/ajmg.b.32648. https://pubmed.ncbi.nlm.nih.gov/30450701/
2. Nishiyama, Kanako, Maekawa, Masashi, Nakagita, Tomoya, Takada, Yasutsugu, Higashiyama, Shigeki. 2021. CNKSR1 serves as a scaffold to activate an EGFR phosphatase via exclusive interaction with RhoB-GTP. In Life science alliance, 4, . doi:10.26508/lsa.202101095. https://pubmed.ncbi.nlm.nih.gov/34187934/
3. Wang, Lei, Liu, Xudong, Yue, Miao, Feng, Dayun, Song, Xinqiang. 2021. Identification of hub genes in bladder cancer based on weighted gene co-expression network analysis from TCGA database. In Cancer reports (Hoboken, N.J.), 5, e1557. doi:10.1002/cnr2.1557. https://pubmed.ncbi.nlm.nih.gov/34541834/
4. Chen, Junhong, Jin, Hengwei, Zhou, Hao, Hei, Xufei, Liu, Kai. 2023. Research into the characteristic molecules significantly affecting liver cancer immunotherapy. In Frontiers in immunology, 14, 1029427. doi:10.3389/fimmu.2023.1029427. https://pubmed.ncbi.nlm.nih.gov/36860864/
5. Zarei Ghobadi, Mohadeseh, Afsaneh, Elaheh, Emamzadeh, Rahman. 2023. Gene biomarkers and classifiers for various subtypes of HTLV-1-caused ATLL cancer identified by a combination of differential gene co‑expression and support vector machine algorithms. In Medical microbiology and immunology, 212, 263-270. doi:10.1007/s00430-023-00767-8. https://pubmed.ncbi.nlm.nih.gov/37222763/