1. Chen, Chun-Wei, Zhang, Linda, Dutta, Ravi, Sperling, Adam S, Goodell, Margaret A. 2023. SRCAP mutations drive clonal hematopoiesis through epigenetic and DNA repair dysregulation. In Cell stem cell, 30, 1503-1519.e8. doi:10.1016/j.stem.2023.09.011. https://pubmed.ncbi.nlm.nih.gov/37863054/
2. Rots, Dmitrijs, Chater-Diehl, Eric, Dingemans, Alexander J M, Koolen, David A, Weksberg, Rosanna. 2021. Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature. In American journal of human genetics, 108, 1053-1068. doi:10.1016/j.ajhg.2021.04.008. https://pubmed.ncbi.nlm.nih.gov/33909990/
3. Zhang, Huixia, Li, Shasha, Zhou, Runxin, Yang, Xiang-Ping, Sun, Shuguo. 2024. SRCAP complex promotes lung cancer progression by reprograming the oncogenic transcription of Hippo-YAP/TAZ signaling pathway. In Cancer letters, 585, 216667. doi:10.1016/j.canlet.2024.216667. https://pubmed.ncbi.nlm.nih.gov/38280479/
4. Ding, Chaodong, Zhou, Wei, Shi, Yuhan, Li, Fei, Qiu, Zilong. 2024. Srcap haploinsufficiency induced autistic-like behaviors in mice through disruption of Satb2 expression. In Cell reports, 43, 114231. doi:10.1016/j.celrep.2024.114231. https://pubmed.ncbi.nlm.nih.gov/38733588/
5. Välimäki, Niko, Jokinen, Vilja, Cajuso, Tatiana, Aaltonen, Lauri A, Karhu, Auli. 2023. Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas. In American journal of human genetics, 110, 460-474. doi:10.1016/j.ajhg.2023.01.009. https://pubmed.ncbi.nlm.nih.gov/36773604/
6. Mouradov, Dmitri, Sloggett, Clare, Jorissen, Robert N, Mariadason, John M, Sieber, Oliver M. 2014. Colorectal cancer cell lines are representative models of the main molecular subtypes of primary cancer. In Cancer research, 74, 3238-47. doi:10.1158/0008-5472.CAN-14-0013. https://pubmed.ncbi.nlm.nih.gov/24755471/