Zou T, Zhou M, Gupta A, et al. deletion induces PKR-dependent cell lethality in interferon-activated cancer cells. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.08.01.551488
Publications
Ilia K, Shakiba N, Bingham T, et al. Synthetic genetic circuits to uncover and enforce the OCT4 trajectories of successful reprogramming of human fibroblasts. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.01.25.525529
Lassen FH, Venkatesh SS, Baya N, et al. Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.29.23291992
Stenton SL, O’Leary M, Lemire G, et al. Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.08.02.23293212
Mead BE, Kummerlowe C, Liu N, et al. Compressed phenotypic screens for complex multicellular models and high-content assays. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.01.23.525189
Rämö JT, Kany S, Hou CR, et al. The Cardiovascular Impact and Genetics of Pericardial Adiposity. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.07.16.23292729
Nameki RA, Chang H, Yu P, et al. Rewiring of master transcription factor cistromes during high-grade serous ovarian cancer development. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.04.11.536378
Kentistou KA, Kaisinger LR, Stankovic S, et al. Understanding the genetic complexity of puberty timing across the allele frequency spectrum. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.06.14.23291322
Tadros R, Zheng SL, Grace C, et al. Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.01.28.23285147
Georgeson P, Steinfelder RS, Harrison TA, et al. Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.03.10.23287127