1. Weishaupt, Holger, Čančer, Matko, Rosén, Gabriela, Ameur, Adam, Swartling, Fredrik J. . Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas. In Neuro-oncology, 25, 97-107. doi:10.1093/neuonc/noac158. https://pubmed.ncbi.nlm.nih.gov/35738865/
2. Dong, Caihua, Li, Xinying, Yang, Jiao, Fu, Peng, Sun, Minxuan. 2021. PPFIBP1 induces glioma cell migration and invasion through FAK/Src/JNK signaling pathway. In Cell death & disease, 12, 827. doi:10.1038/s41419-021-04107-7. https://pubmed.ncbi.nlm.nih.gov/34480020/
3. Waqas, Ahmed, Liaqat, Romana, Shaheen, Sidrah, Umair, Muhammad, Abbas, Safdar. 2022. A novel homozygous truncating variant in PPFIBP1 further delineates PPFIBP1-associated neurodevelopmental disorder. In International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 83, 191-200. doi:10.1002/jdn.10247. https://pubmed.ncbi.nlm.nih.gov/36527195/
4. Gao, Qichang, Ma, Yiming, Shao, Tuo, Gu, Jiaao, Yu, Zhange. 2024. Development and Validation of Diagnostic Models for Transcriptomic Signature Genes for Multiple Tissues in Osteoarthritis. In Journal of inflammation research, 17, 5113-5127. doi:10.2147/JIR.S472118. https://pubmed.ncbi.nlm.nih.gov/39099665/
5. Takeuchi, Kengo, Soda, Manabu, Togashi, Yuki, Mano, Hiroyuki, Ishikawa, Yuichi. 2011. Pulmonary inflammatory myofibroblastic tumor expressing a novel fusion, PPFIBP1-ALK: reappraisal of anti-ALK immunohistochemistry as a tool for novel ALK fusion identification. In Clinical cancer research : an official journal of the American Association for Cancer Research, 17, 3341-8. doi:10.1158/1078-0432.CCR-11-0063. https://pubmed.ncbi.nlm.nih.gov/21430068/
6. Dickson, Brendan C, Swanson, David, Charames, George S, Fletcher, Christopher Dm, Hornick, Jason L. 2018. Epithelioid fibrous histiocytoma: molecular characterization of ALK fusion partners in 23 cases. In Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 31, 753-762. doi:10.1038/modpathol.2017.191. https://pubmed.ncbi.nlm.nih.gov/29327718/
7. Ben-Mahmoud, Afif, Kishikawa, Shotaro, Gupta, Vijay, Layman, Lawrence C, Kim, Hyung-Goo. 2023. A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome. In Scientific reports, 13, 12984. doi:10.1038/s41598-023-40037-4. https://pubmed.ncbi.nlm.nih.gov/37563198/