Blokland GAM, Maleki N, Jovicich J, et al. MIR137 polygenic risk for schizophrenia and ephrin-regulated pathway: Role in lateral ventricles and corpus callosum volume. International journal of clinical and health psychology : IJCHP. 2024;24(2):100458. doi:10.1016/j.ijchp.2024.100458DOIGoogle ScholarPubMed
Publications
Wigdor EM, Samocha KE, Eberhardt RY, et al. Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders. Scientific reports. 2024;14(1):8708. doi:10.1038/s41598-024-58894-yDOIGoogle ScholarPubMed
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
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.0000000000001780DOIGoogle ScholarPubMed
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:10.1101/2024.03.28.24305045DOIGoogle ScholarPubMed
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:10.1101/2024.03.25.24304535DOIGoogle ScholarPubMed
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:10.1101/2024.03.20.585828DOIGoogle ScholarPubMed