Zhou Y, Ahsan FM, Emans SW, Soukas AA. The nuclear pore complex connects energy sensing to transcriptional plasticity in longevity. Molecular cell. 2025. doi:10.1016/j.molcel.2025.08.035
Publications
Siddiqui SM, Welch NL, Nguyen TG, et al. Bead-based approaches for increased sensitivity and multiplexing of CRISPR diagnostics. Nature biomedical engineering. 2025. doi:10.1038/s41551-025-01498-2
Li Z, Patel ZM, Song D, et al. Systematic benchmarking of computational methods to identify spatially variable genes. Genome biology. 2025;26(1):285. doi:10.1186/s13059-025-03731-2
Arriaga TM, Mendez R, Ungar RA, et al. Transcriptome-wide outlier approach identifies individuals with minor spliceopathies. American journal of human genetics. 2025. doi:10.1016/j.ajhg.2025.08.018
Knudsen NH, Escobar G, Korell F, et al. In vivo CRISPR screens identify modifiers of CAR T cell function in myeloma. Nature. 2025. doi:10.1038/s41586-025-09489-8
Steinicke TL, Benfatto S, Capilla-Guerra MR, et al. Rapid epigenomic classification of acute leukemia. Nature genetics. 2025. doi:10.1038/s41588-025-02321-z
Xu J, Kong L, Creasey EA, et al. Autoimmune disease risk gene ANKRD55 promotes TH17 effector function through metabolic modulation. The Journal of experimental medicine. 2025;222(11). doi:10.1084/jem.20250185
Jurgens SJ, Melloni GEM, Kany S, et al. Pathogenic Cardiomyopathy-Associated Gene Variants and Prognosis in Atrial Fibrillation: Results in 18,000 Clinical Trial Participants. Journal of the American College of Cardiology. 2025;86(10):738-753. doi:10.1016/j.jacc.2025.06.052
Roh H, Shen S, Hu Y, et al. Coupling CRISPR scanning with targeted chromatin accessibility profiling using a double-stranded DNA deaminase. Nature methods. 2025. doi:10.1038/s41592-025-02811-2
Karczewski K, Gupta R, Kanai M, et al. Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effects. Nature genetics. 2025. doi:10.1038/s41588-025-02335-7