Paull JS, Petros BA, Brock-Fisher TM, et al. Optimisation and evaluation of viral genomic sequencing of SARS-CoV-2 rapid diagnostic tests: a laboratory and cohort-based study. The Lancet. Microbe. 2024. doi:10.1016/S2666-5247(23)00399-3DOIGoogle ScholarPubMed
Publications
Postek W, Staśkiewicz K, Lilja E, Wacław B. Substrate geometry affects population dynamics in a bacterial biofilm. Proceedings of the National Academy of Sciences of the United States of America. 2024;121(17):e2315361121. doi:10.1073/pnas.2315361121DOIGoogle ScholarPubMed
Lee LJ, Bungart B, Wainger B, Gorky J, So A, Wang J. Transient Acute Diplopia as a Rare Side Effect of Hydromorphone: A Case Report. A&A practice. 2024;18(4):e01780. doi:10.1213/XAA.0000000000001780PubMedDOIGoogle Scholar
Strayer N, Vessels T, Choi K, et al. Interoperability of phenome-wide multimorbidity patterns: a comparative study of two large-scale EHR systems. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.03.28.24305045PubMedDOIGoogle Scholar
Tse MW, Zhu M, Peters B, et al. Massively parallel combination screen reveals small molecule sensitization of antibiotic-resistant Gram-negative ESKAPE pathogens. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.26.586803DOIGoogle ScholarPubMed
Silverstein S, Orbach R, Syeda S, et al. Differential inclusion of exons 143 and 144 provides insight into -related myopathy variant interpretation and disease manifestation. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.03.25.24304535PubMedDOIGoogle Scholar
Foley R, Bolduc V, Guirguis F, et al. The recurrent deep intronic pseudoexon-inducing variant c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.03.29.24304673DOIGoogle ScholarPubMed
Jayne L, Lavin-Peter A, Roessler J, et al. A torpor-like state (TLS) in mice slows blood epigenetic aging and prolongs healthspan. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.20.585828PubMedDOIGoogle Scholar
Clauwaert J, McVey Z, Gupta R, Yannuzzi I, Menschaert G, Prensner JR. Deep learning to decode sites of RNA translation in normal and cancerous tissues. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.21.586110PubMedDOIGoogle Scholar
Marin MG, Wippel C, Quinones-Olvera N, et al. Analysis of the limited accessory genome reveals potential pitfalls of pan-genome analysis approaches. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.03.21.586149DOIGoogle ScholarPubMed