Claussnitzer M, Parikh VN, Wagner AH, et al. Minimum information and guidelines for reporting a multiplexed assay of variant effect. Genome biology. 2024;25(1):100. doi:10.1186/s13059-024-03223-9
Baglaenko Y, Wagner C, Bhoj VG, et al. Making inroads to precision medicine for the treatment of autoimmune diseases: Harnessing genomic studies to better diagnose and treat complex disorders. Cambridge prisms. Precision medicine. 2023;1:e25. doi:10.1017/pcm.2023.14
Mendez KM, Begum S, Tiwari A, et al. Metabolite signatures associated with microRNA miR-143-3p serve as drivers of poor lung function trajectories in childhood asthma. EBioMedicine. 2024;102:105025. doi:10.1016/j.ebiom.2024.105025
Anderson JA, Lin D, Lea AJ, et al. DNA methylation signatures of early-life adversity are exposure-dependent in wild baboons. Proceedings of the National Academy of Sciences of the United States of America. 2024;121(11):e2309469121. doi:10.1073/pnas.2309469121
Schwartzman JA, Lebreton F, Salamzade R, et al. Global diversity of enterococci and description of 18 previously unknown species. Proceedings of the National Academy of Sciences of the United States of America. 2024;121(10):e2310852121. doi:10.1073/pnas.2310852121
Sud A, Parry EM, Wu CJ. The molecular map of CLL and Richter’s syndrome. Seminars in hematology. 2024. doi:10.1053/j.seminhematol.2024.01.009
Schuermans A, Vlasschaert C, Nauffal V, et al. Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias. European heart journal. 2023. doi:10.1093/eurheartj/ehad670
McClellan JM, Zoghbi AW, Buxbaum JD, et al. An evolutionary perspective on complex neuropsychiatric disease. Neuron. 2024;112(1):7-24. doi:10.1016/j.neuron.2023.10.037
Raghavan A, Pirruccello JP, Ellinor PT, Lindsay ME. Using Genomics to Identify Novel Therapeutic Targets for Aortic Disease. Arteriosclerosis, thrombosis, and vascular biology. 2023. doi:10.1161/ATVBAHA.123.318771
Seaby EG, Thomas S, Hunt D, et al. A Panel-Agnostic Strategy ’HiPPo’ Improves Diagnostic Efficiency in the UK Genomic Medicine Service. Healthcare (Basel, Switzerland). 2023;11(24). doi:10.3390/healthcare11243179