1. Lu, Chuncheng, Zhang, Yan, Qin, Yufeng, Wang, Xinru, Xia, Yankai. 2020. Human X chromosome exome sequencing identifies BCORL1 as contributor to spermatogenesis. In Journal of medical genetics, 58, 56-65. doi:10.1136/jmedgenet-2019-106598. https://pubmed.ncbi.nlm.nih.gov/32376790/
2. Chang, Ya-Sian, Huang, Hsien-Da, Yeh, Kun-Tu, Chang, Jan-Gowth. 2017. Identification of novel mutations in endometrial cancer patients by whole-exome sequencing. In International journal of oncology, 50, 1778-1784. doi:10.3892/ijo.2017.3919. https://pubmed.ncbi.nlm.nih.gov/28339086/
3. Rajalingam, Aruna, Sekar, Kanagaraj, Ganjiwale, Anjali. . Identification of Potential Genes and Critical Pathways in Postoperative Recurrence of Crohn's Disease by Machine Learning And WGCNA Network Analysis. In Current genomics, 24, 84-99. doi:10.2174/1389202924666230601122334. https://pubmed.ncbi.nlm.nih.gov/37994325/
4. Zhang, Baojian, Li, Biao, Sun, Chao, Xiao, Yichao, Liu, Qiming. 2021. Identification of key gene modules and pathways of human platelet transcriptome in acute myocardial infarction patients through co-expression network. In American journal of translational research, 13, 3890-3905. doi:. https://pubmed.ncbi.nlm.nih.gov/34017580/
5. Yang, Yeran, Liu, Wei, Jin, Yaqiong, Zhang, Jie, Ni, Xin. 2021. Identification of potential pathogenic mutations in Chinese children with first branchial cleft anomalies detected by whole-exome sequencing. In Pediatric investigation, 5, 211-216. doi:10.1002/ped4.12263. https://pubmed.ncbi.nlm.nih.gov/34589676/