Strom NI, Gerring ZF, Galimberti M, et al. Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. Nature genetics. 2025;57(6):1389-1401. doi:10.1038/s41588-025-02189-z
Publications
Zhang X, Tseo Y, Bai Y, Chen F, Uhler C. Prediction of protein subcellular localization in single cells. Nature methods. 2025;22(6):1265-1275. doi:10.1038/s41592-025-02696-1
Choksi D, Gutiérrez-MartÃnez L, Rist PM, et al. Use of the Brain Care Score to Estimate the Risk of Incident Cerebrovascular Events in Middle-Aged Women. Neurology. 2025;104(11):e213674. doi:10.1212/WNL.0000000000213674
Horsdal HT, Albiñana C, Zhu Z, et al. Convergent evidence linking neonatal vitamin D status and risk of neurodevelopmental disorders: a Danish case-cohort study. The lancet. Psychiatry. 2025;12(6):410-420. doi:10.1016/S2215-0366(25)00099-9
Nava C, Cogne B, Santini A, et al. Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption. Nature genetics. 2025;57(6):1374-1388. doi:10.1038/s41588-025-02184-4
Zhang Y, Sakaue S, Morris S, et al. The contribution of gametic phase disequilibrium to the heritability of complex traits. Nature genetics. 2025;57(6):1418-1425. doi:10.1038/s41588-025-02192-4
Braun F, Mandel AM, Blomberg L, et al. Loss of genome maintenance is linked to mTOR complex 1 signaling and accelerates podocyte damage. JCI insight. 2025;10(12). doi:10.1172/jci.insight.172370
Alberge JB, Dutta AK, Poletti A, et al. Genomic landscape of multiple myeloma and its precursor conditions. Nature genetics. 2025;57(6):1493-1503. doi:10.1038/s41588-025-02196-0
Lammi V, Nakanishi T, Jones SE, et al. Genome-wide association study of long COVID. Nature genetics. 2025;57(6):1402-1417. doi:10.1038/s41588-025-02100-w
Yuan WC, Earl AS, Ma S, et al. HBO1 functions as an epigenetic barrier to hepatocyte plasticity and reprogramming during liver injury. Cell stem cell. 2025;32(6):990-1005.e8. doi:10.1016/j.stem.2025.04.010