Pașca SP, Arlotta P, Bateup HS, et al. A framework for neural organoids, assembloids and transplantation studies. Nature. 2024. doi:10.1038/s41586-024-08487-6
Publications
Wong F, Omori S, Li A, et al. An explainable deep learning platform for molecular discovery. Nature protocols. 2024. doi:10.1038/s41596-024-01084-x
Camp SY, He MX, Cuoco MS, et al. Single-cell epigenetic profiling reveals an interferon response-high program associated with deficiency in kidney cancer. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.11.15.623837
Rominger MC, Gupta S, Moorthi S, et al. Mutant RIT1 cooperates with YAP to drive an EMT-like lung cancer state. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.11.11.623044
Corridon TL, O’Moore J, Lian Y, et al. PrP turnover in vivo and the time to effect of prion disease therapeutics. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.11.12.623215
Fan Y, Chen J, Fan Z, et al. Mapping rare protein-coding variants on multi-organ imaging traits. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.11.16.24317443
Bennett G, Karbassi I, Chen W, et al. Distinct rates of VUS reclassification are observed when subclassifying VUS by evidence level. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.11.13.24317242
Ma R, Conley SD, Kosicki M, et al. Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heart. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.11.20.24317557
Broeren E, Gitau V, Byrne A, et al. The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.11.19.24317561
Amrute JM, Lee PC, Eres I, et al. Single cell variant to enhancer to gene map for coronary artery disease. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.11.13.24317257