1. Nijboer, Tanja C W, Hessel, Ellen V S, van Haaften, Gijs W, Brilstra, Eva H, Burbach, J Peter H. 2023. Identification of candidate genes for developmental colour agnosia in a single unique family. In PloS one, 18, e0290013. doi:10.1371/journal.pone.0290013. https://pubmed.ncbi.nlm.nih.gov/37672513/
2. Kajii, Takashi S, Oka, Akira, Saito, Fumio, Mitsui, Jun, Iida, Junichiro. 2019. Whole-exome sequencing in a Japanese pedigree implicates a rare non-synonymous single-nucleotide variant in BEST3 as a candidate for mandibular prognathism. In Bone, 122, 193-198. doi:10.1016/j.bone.2019.03.004. https://pubmed.ncbi.nlm.nih.gov/30849546/
3. Wu, Yingcheng, Wei, Jinhuan, Ming, Yue, Zhou, Guoxiong, Fan, Yihui. 2018. Orchestrating a biomarker panel with lncRNAs and mRNAs for predicting survival in pancreatic ductal adenocarcinoma. In Journal of cellular biochemistry, 119, 7696-7706. doi:10.1002/jcb.27119. https://pubmed.ncbi.nlm.nih.gov/29923223/
4. Lessard, Christopher J, Adrianto, Indra, Ice, John A, Montgomery, Courtney G, Moser, Kathy L. 2012. Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study. In American journal of human genetics, 90, 648-60. doi:10.1016/j.ajhg.2012.02.023. https://pubmed.ncbi.nlm.nih.gov/22464253/