Byrne SR, DeMott MS, Yuan Y, et al. Temporal dynamics and metagenomics of phosphorothioate epigenomes in the human gut microbiome. Microbiome. 2025;13(1):81. doi:10.1186/s40168-025-02071-4
Publications
Jeong S, Lin L, Leone AP, Hsu YH. Type 2 diabetes and late-onset Alzheimer’s disease and related dementia: A longitudinal cohort study integrating polygenic risk score. Journal of Alzheimer’s disease : JAD. 2025:13872877251326107. doi:10.1177/13872877251326107
Khirallah J, Bloomer H, Wich D, et al. base editing of Angptl3 via lipid nanoparticles to treat cardiovascular disease. Molecular therapy. Nucleic acids. 2025;36(2):102486. doi:10.1016/j.omtn.2025.102486
Islam MM, Tamlander M, Hlushchenko I, Ripatti S, Pfisterer SG. Large-Scale Functional Characterization of Low-Density Lipoprotein Receptor Gene Variants Improves Risk Assessment in Cardiovascular Disease. JACC. Basic to translational science. 2025;10(2):170-183. doi:10.1016/j.jacbts.2024.10.006
Acera-Mateos M, Adiconis X, Li JK, et al. Systematic evaluation of single-cell multimodal data integration for comprehensive human reference atlas. bioRxiv : the preprint server for biology. 2025. doi:10.1101/2025.03.06.637075
Sarto F, Fry CS, Narici M V, Rubin L, Price FD. Potential of synergist ablation to study mechanisms of skeletal muscle hypertrophy in rodent disease models. American journal of physiology. Cell physiology. 2025. doi:10.1152/ajpcell.00076.2025
Fernandes TAA, Tourville A, Ciss I, et al. Oxytetracycline and its Non-Antibiotic Derivative DOT Protect Midbrain Dopamine Neurons from Iron-Driven Oxidative Damage. Neurotoxicity research. 2025;43(2):16. doi:10.1007/s12640-025-00742-6
Georgakis MK, Malik R, Bounkari OE, et al. Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk. Genome medicine. 2025;17(1):27. doi:10.1186/s13073-025-01456-2
Do C, Jiang G, Cova G, et al. Binding domain mutations provide insight into CTCF’s relationship with chromatin and its contribution to gene regulation. Cell genomics. 2025:100813. doi:10.1016/j.xgen.2025.100813
Schwartzman WE, Hujoel MLA, Channaoui N, Lee-Kim V, Loh PR, Gupta RM. Interpreting MYH11 Copy Number Variation in Thoracic Aortic Aneurysm and Dissection: Insights From the Misannotation of Variants in Clinical Genetic Tests. JACC. Case reports. 2025;30(6 Pt 1):102973. doi:10.1016/j.jaccas.2024.102973