1. Wang, Qiming, Chen, Shaopeng, Wang, Gang, Zhang, Tielong, Gao, Yulong. 2024. Integrated mendelian randomization analyses highlight AFF3 as a novel eQTL-mediated susceptibility gene in renal cancer and its potential mechanisms. In BMC cancer, 24, 739. doi:10.1186/s12885-024-12513-1. https://pubmed.ncbi.nlm.nih.gov/38886730/
2. Ali, Yasir, Khan, Suleman, Chen, Yangchao, Jamal, Muhsin, Jalil, Fazal. 2021. Association of AFF3 Gene Polymorphism rs10865035 with Rheumatoid Arthritis: A Population-Based Case-Control Study on a Pakistani Cohort. In Genetics research, 2021, 5544198. doi:10.1155/2021/5544198. https://pubmed.ncbi.nlm.nih.gov/34104118/
3. Bassani, Sissy, Chrast, Jacqueline, Ambrosini, Giovanna, Guex, Nicolas, Reymond, Alexandre. 2024. Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles. In Genome medicine, 16, 72. doi:10.1186/s13073-024-01339-y. https://pubmed.ncbi.nlm.nih.gov/38811945/
4. Sun, Difan, Du, Xinyu, Su, Peng. 2024. Molecular evolution of transcription factors AF4/FMR2 family member (AFF) gene family and the role of lamprey AFF3 in cell proliferation. In Development genes and evolution, 234, 45-53. doi:10.1007/s00427-024-00717-1. https://pubmed.ncbi.nlm.nih.gov/38733410/
5. Moore, Justin M, Oliver, Peter L, Finelli, Mattéa J, Molnár, Zoltán, Davies, Kay E. 2014. Laf4/Aff3, a gene involved in intellectual disability, is required for cellular migration in the mouse cerebral cortex. In PloS one, 9, e105933. doi:10.1371/journal.pone.0105933. https://pubmed.ncbi.nlm.nih.gov/25162227/
6. Tsukumo, Shin-Ichi, Subramani, Poorani Ganesh, Seija, Noé, Di Noia, Javier M, Yasutomo, Koji. 2022. AFF3, a susceptibility factor for autoimmune diseases, is a molecular facilitator of immunoglobulin class switch recombination. In Science advances, 8, eabq0008. doi:10.1126/sciadv.abq0008. https://pubmed.ncbi.nlm.nih.gov/36001653/
7. Jadhav, Bharati, Garg, Paras, van Vugt, Joke J F A, Tucci, Arianna, Sharp, Andrew J. 2024. A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability. In Nature genetics, 56, 2322-2332. doi:10.1038/s41588-024-01917-1. https://pubmed.ncbi.nlm.nih.gov/39313615/
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