Toikumo S, Jennings M V, Pham BK, et al. Multi-ancestry meta-analysis of tobacco use disorder identifies 461 potential risk genes and reveals associations with multiple health outcomes. Nature human behaviour. 2024. doi:10.1038/s41562-024-01851-6DOIPubMedGoogle Scholar
Publications
Minikel EV, Painter JL, Dong CC, Nelson MR. Refining the impact of genetic evidence on clinical success. Nature. 2024. doi:10.1038/s41586-024-07316-0DOIPubMedGoogle Scholar
Minikel EV, Painter JL, Dong CC, Nelson MR. Refining the impact of genetic evidence on clinical success. Nature. 2024. doi:10.1038/s41586-024-07316-0DOIPubMedGoogle Scholar
Choi J, Lee EA. Analysis of REST binding sites with canonical and non-canonical motifs in human cell lines. BMC medical genomics. 2024;17(Suppl 1):92. doi:10.1186/s12920-024-01860-4DOIPubMedGoogle Scholar
Roh JD, Castro C, Yu A, et al. Placental senescence pathophysiology is shared between peripartum cardiomyopathy and preeclampsia in mouse and human. Science translational medicine. 2024;16(743):eadi0077. doi:10.1126/scitranslmed.adi0077DOIPubMedGoogle Scholar
Cacheiro P, Lawson S, Van den Veyver IB, et al. Lethal phenotypes in Mendelian disorders. Genetics in medicine : official journal of the American College of Medical Genetics. 2024:101141. doi:10.1016/j.gim.2024.101141DOIPubMedGoogle Scholar
Hayes TK, Aquilanti E, Persky NS, et al. Author Correction: Comprehensive mutational scanning of EGFR reveals TKI sensitivities of extracellular domain mutants. Nature communications. 2024;15(1):3273. doi:10.1038/s41467-024-47675-wDOIPubMedGoogle Scholar
Hivert MF, White F, Allard C, et al. Placental IGFBP1 levels during early pregnancy and the risk of insulin resistance and gestational diabetes. Nature medicine. 2024. doi:10.1038/s41591-024-02936-5DOIPubMedGoogle Scholar
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.2024.100458DOIPubMedGoogle Scholar
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-yDOIPubMedGoogle Scholar