Urbut SM, Koyama S, Hornsby W, et al. Bayesian multivariate genetic analysis improves translational insights. iScience. 2023;26(10):107854. doi:10.1016/j.isci.2023.107854
Publications
Kamphuis P, van Zeventer IA, de Graaf AO, et al. Clonal Hematopoiesis Defined by Somatic Mutations Infrequently Co-occurs With Mosaic Loss of the Y Chromosome in a Population-based Cohort. HemaSphere. 2023;7(10):e956. doi:10.1097/HS9.0000000000000956
Kamphuis P, van Zeventer IA, de Graaf AO, et al. Clonal Hematopoiesis Defined by Somatic Mutations Infrequently Co-occurs With Mosaic Loss of the Y Chromosome in a Population-based Cohort. HemaSphere. 2023;7(10):e956. doi:10.1097/HS9.0000000000000956
Ibrahim MK, Wilechansky RM, Challa PK, et al. The empirical dietary inflammatory pattern score and the risk of nonalcoholic fatty liver disease and cirrhosis. Hepatology communications. 2023;7(10). doi:10.1097/HC9.0000000000000263
Maisat W, Yuki K. Volatile anesthetic isoflurane exposure facilitates Enterococcus biofilm infection. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2023;37(10):e23186. doi:10.1096/fj.202301128R
Gold JI, Madhavan S, Park J, et al. Phenotypes of undiagnosed adults with actionable and variants. HGG advances. 2023;4(4):100226. doi:10.1016/j.xhgg.2023.100226
Collier JL, Pauken KE, Lee CAA, et al. Single-cell profiling reveals unique features of diabetogenic T cells in anti-PD-1-induced type 1 diabetes mice. The Journal of experimental medicine. 2023;220(10). doi:10.1084/jem.20221920
Mourtzi N, Charisis S, Tsapanou A, et al. Genetic propensity for cerebral amyloidosis and risk of mild cognitive impairment and Alzheimer’s disease within a cognitive reserve framework. Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 2023;19(9):3794-3805. doi:10.1002/alz.12980
Manning A, Sevilla-Gonzalez M, Smith K, et al. Heterogeneous effects on type 2 diabetes and cardiovascular outcomes of genetic variants and traits associated with fasting insulin. Research square. 2023. doi:10.21203/rs.3.rs-3317661/v1
Rauch PJ, Gopakumar J, Silver AJ, et al. Loss-of-function mutations in Dnmt3a and Tet2 lead to accelerated atherosclerosis and concordant macrophage phenotypes. Nature cardiovascular research. 2023;2(9):805-818. doi:10.1038/s44161-023-00326-7