Cui J, Yu Z, Oakes EG, et al. Clonal haematopoiesis and risk of incident rheumatoid arthritis: results from the UK biobank. Clinical and experimental rheumatology. 2026. doi:10.55563/clinexprheumatol/23hcbl
Publications
Spinks C, Selvaraj MS, Robinson C, et al. Management and Consequences of Genotype-Positive Familial Hypercholesterolemia. JAMA cardiology. 2026. doi:10.1001/jamacardio.2026.0006
Ohlstrom DJ, Pilcher WC, Michaud ME, et al. Longitudinal Profiling of Tumor and Immune Compartments Uncovers Patterns of Dysregulation and Associations with Response in Multiple Myeloma. Blood cancer discovery. 2026;7(2):266-286. doi:10.1158/2643-3230.BCD-25-0205
Rauch DE, Wang M, Hafiz MJH, et al. Assessment of In-Frame Indel Variants in an Unsolved Cohort of Inherited Retinal Diseases Using Machine Learning. Human mutation. 2026;2026:3902530. doi:10.1155/humu/3902530
PMCID
PMC12951207
Hong EP, Ha EJ, Youn DH, et al. Whole-Exome Sequencing Improves Risk Assessments of Adult Moyamoya Disease. Journal of clinical neurology (Seoul, Korea). 2026;22(2):160-172. doi:10.3988/jcn.2025.0482
Shi Y, Cheng KY, Thi TT, et al. GPR146 in adipose tissue drives adipose-liver crosstalk and promotes hepatic steatosis in mice. Nature communications. 2026. doi:10.1038/s41467-026-70136-5
Yu Q, Liu H, Shi H, et al. Uncovering evolutionarily remote and highly potent antimicrobial peptides with protein language models. Nature biomedical engineering. 2026. doi:10.1038/s41551-026-01630-w
Ayub-Ferreira SM, Avila MS, Wanderley MR de B, et al. Carvedilol for Prevention of Chemotherapy-Induced Cardiotoxicity: Final Results of the CECCY Trial. JACC. CardioOncology. 2026. doi:10.1016/j.jaccao.2025.12.009
Skinner OS, Miranda M, Dong F, et al. 4,5-dihydroxyhexanoic acid is a robust circulating and urine marker of mitochondrial disease and its severity. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.02.10.705117
PMCID
PMC12918946
Zangas P, Omarov M, Georgakis MK. Genetically Simulated GLP-1 Receptor Agonism and Cerebral Small Vessel Disease. Neurology. Genetics. 2026;12(2):e200359. doi:10.1212/NXG.0000000000200359
PMCID
PMC12947837