1. Barish, Scott, Barakat, Tahsin Stefan, Michel, Brittany C, Scott, Daryl A, Bellen, Hugo J. 2020. BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. In American journal of human genetics, 107, 1096-1112. doi:10.1016/j.ajhg.2020.11.003. https://pubmed.ncbi.nlm.nih.gov/33232675/
2. Schmetz, Ariane, Lüdecke, Hermann-Josef, Surowy, Harald, Bramswig, Nuria C, Wieczorek, Dagmar. 2023. Delineation of the adult phenotype of Coffin-Siris syndrome in 35 individuals. In Human genetics, 143, 71-84. doi:10.1007/s00439-023-02622-5. https://pubmed.ncbi.nlm.nih.gov/38117302/
3. Sun, Ying, Li, Zhuojie, Li, Wenzhe, Xue, Lei. 2021. Loss of Bicra impairs Drosophila learning and choice abilities. In Neuroscience letters, 769, 136432. doi:10.1016/j.neulet.2021.136432. https://pubmed.ncbi.nlm.nih.gov/34974109/
4. Tu, Youquan, Fang, Chunyan, Xu, Jian, Liang, Mengmeng, Yang, Zuozhen. 2023. A de novo variant of BICRA results in Coffin-Siris syndrome 12. In Molecular genetics & genomic medicine, 11, e2250. doi:10.1002/mgg3.2250. https://pubmed.ncbi.nlm.nih.gov/37485815/
5. Asadauskaitė, Greta, Morkūnienė, Aušra, Utkus, Algirdas, Burnytė, Birutė. 2022. Identification of a novel BICRA variant leading to the newly described Coffin-Siris syndrome 12. In Brain & development, 45, 185-190. doi:10.1016/j.braindev.2022.11.003. https://pubmed.ncbi.nlm.nih.gov/36437209/
6. Mullin, Benjamin H, Zhu, Kun, Brown, Suzanne J, Xu, Jiake, Wilson, Scott G. . Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis. In Genetics, 225, . doi:10.1093/genetics/iyad150. https://pubmed.ncbi.nlm.nih.gov/37579195/
7. Schrier Vergano, Samantha A. 2024. ARID2, a milder cause of Coffin-Siris Syndrome? Broadening the phenotype with 17 additional individuals. In American journal of medical genetics. Part A, 194, e63540. doi:10.1002/ajmg.a.63540. https://pubmed.ncbi.nlm.nih.gov/38243407/