Kelley ME, Berman AY, Stirling DR, et al. High-content microscopy reveals a morphological signature of bortezomib resistance. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.05.02.539137
Publications
Gazestani V, Kamath T, Nadaf NM, et al. Early Alzheimer’s disease pathology in human cortex is associated with a transient phase of distinct cell states. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.06.03.543569
Huang Y, Durall T, Luong NM, et al. EZH2 synergizes with BRD4-NUT to drive NUT carcinoma growth through silencing of key tumor suppressor genes. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.08.15.553204
Szczerbiński L, Florez JC. Precision medicine of obesity as an integral part of type 2 diabetes management - past, present, and future. The lancet. Diabetes & endocrinology. 2023. doi:10.1016/S2213-8587(23)00232-2
Franks PW, Cefalu WT, Dennis J, et al. Precision medicine for cardiometabolic disease: a framework for clinical translation. The lancet. Diabetes & endocrinology. 2023. doi:10.1016/S2213-8587(23)00165-1
Xiao Q, Mears J, Nathan A, et al. Immunosuppression causes dynamic changes in expression QTLs in psoriatic skin. Nature communications. 2023;14(1):6268. doi:10.1038/s41467-023-41984-2
Barner LAE, Gao G, Reddi DM, et al. AI-Triaged 3D Pathology to Improve Detection of Esophageal Neoplasia While Reducing Pathologist Workloads. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 2023;36(12):100322. doi:10.1016/j.modpat.2023.100322
Mekbib KY, Muñoz W, Allington G, et al. Human genetics and molecular genomics of Chiari malformation type 1. Trends in molecular medicine. 2023. doi:10.1016/j.molmed.2023.08.013
Wang Y, Selvaraj MS, Li X, et al. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. American journal of human genetics. 2023;110(10):1704-1717. doi:10.1016/j.ajhg.2023.09.003
Shi X, Lu C, Corman A, et al. Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction. American journal of human genetics. 2023;110(10):1750-1768. doi:10.1016/j.ajhg.2023.09.004