Lu MY, Chen B, Williamson DFK, et al. A Multimodal Generative AI Copilot for Human Pathology. Nature. 2024. doi:10.1038/s41586-024-07618-3
Publications
Villamor-Payà M, Sanchiz-Calvo M, Smak J, et al. and mutations in a patient with a neurodevelopmental disorder and immunodeficiency. iScience. 2024;27(6):109984. doi:10.1016/j.isci.2024.109984
Lu MY, Chen B, Williamson DFK, et al. A Multimodal Generative AI Copilot for Human Pathology. Nature. 2024. doi:10.1038/s41586-024-07618-3
Razavi S, Wong F, Abubaker-Sharif B, et al. Synthetic control of actin polymerization and symmetry breaking in active protocells. Science advances. 2024;10(24):eadk9731. doi:10.1126/sciadv.adk9731
Satyal U, Valentine H, Liu D, et al. Urine Biopsy as Dynamic Biomarker to Enhance Clinical Staging of Bladder Cancer in Radical Cystectomy Candidates. JCO precision oncology. 2024;8:e2300362. doi:10.1200/PO.23.00362
Koenig Z, Yohannes MT, Nkambule LL, et al. A harmonized public resource of deeply sequenced diverse human genomes. Genome research. 2024. doi:10.1101/gr.278378.123
Vuoksimaa E, Saari TT, Aaltonen A, et al. TWINGEN: protocol for an observational clinical biobank recall and biomarker cohort study to identify Finnish individuals with high risk of Alzheimer’s disease. BMJ open. 2024;14(6):e081947. doi:10.1136/bmjopen-2023-081947
Chung M, Imanaka K, Huang Z, et al. Conditional knockout of Shank3 in the ventral CA1 by quantitative in vivo genome-editing impairs social memory in mice. Nature communications. 2024;15(1):4531. doi:10.1038/s41467-024-48430-x
Jermy B, Läll K, Wolford BN, et al. A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. Nature communications. 2024;15(1):5007. doi:10.1038/s41467-024-48938-2
Liu A, Genovese G, Zhao Y, et al. Genetic drivers and cellular selection of female mosaic X chromosome loss. Nature. 2024. doi:10.1038/s41586-024-07533-7