McGarrity S, Ziehr DR, Austin-Tse CA, Wein MN, Chivukula RR, Oldham WM. Exercise Intolerance and Low Cardiac Filling Pressures in a Woman With a Novel eNOS Mutation. Circulation. Genomic and precision medicine. 2024:e004741. doi:10.1161/CIRCGEN.124.004741
Publications
Kany S, Al-Alusi MA, Rämö JT, et al. Associations of "Weekend Warrior" Physical Activity With Incident Disease and Cardiometabolic Health. Circulation. 2024. doi:10.1161/CIRCULATIONAHA.124.068669
Jeong M, Pazokitoroudi A, Liu Z, Sankararaman S. Scalable summary-statistics-based heritability estimation method with individual genotype level accuracy. Genome research. 2024. doi:10.1101/gr.279207.124
He Y, Lu W, Jee YH, et al. Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.08.25.24312558
Thomas CE, Lin Y, Kim M, et al. Characterization of additive gene-environment interactions for colorectal cancer risk. Epidemiology (Cambridge, Mass.). 2024. doi:10.1097/EDE.0000000000001795
Weitzman ER, . Social complexity of a fentanyl vaccine to prevent opioid overdose conference proceedings: Radcliffe institute for advanced study conference proceedings. Vaccine. 2024:126324. doi:10.1016/j.vaccine.2024.126324
Wang QS, Hasegawa T, Namkoong H, et al. Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevance. Nature genetics. 2024. doi:10.1038/s41588-024-01896-3
Schiffman JS, D’Avino AR, Prieto T, et al. Defining heritability, plasticity, and transition dynamics of cellular phenotypes in somatic evolution. Nature genetics. 2024. doi:10.1038/s41588-024-01920-6
Joseph J, Baby HM, Quintero JR, et al. Toward a Radically Simple Multi-Modal Nasal Spray for Preventing Respiratory Infections. Advanced materials (Deerfield Beach, Fla.). 2024:e2406348. doi:10.1002/adma.202406348
Silverstein S, Orbach R, Syeda S, et al. Differential inclusion of NEB exons 143 and 144 provides insight into NEB-related myopathy variant interpretation and disease manifestation. HGG advances. 2024:100354. doi:10.1016/j.xhgg.2024.100354