Martino D, Schultz N, Kaur R, et al. Respiratory infection- and asthma-prone, low vaccine responder children demonstrate distinct mononuclear cell DNA methylation pathways. Clinical epigenetics. 2024;16(1):85. doi:10.1186/s13148-024-01703-0
Publications
Karchin R, Radivojac P, O’Donnell-Luria A, Greenblatt MS, Tolstorukov MY, Sonkin D. Improving transparency of computational tools for variant effect prediction. Nature genetics. 2024. doi:10.1038/s41588-024-01821-8
Kentistou KA, Kaisinger LR, Stankovic S, et al. Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature genetics. 2024. doi:10.1038/s41588-024-01798-4
Kentistou KA, Kaisinger LR, Stankovic S, et al. Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature genetics. 2024. doi:10.1038/s41588-024-01798-4
Kivimaki M, Frank P, Pentti J, et al. Obesity and risk of diseases associated with hallmarks of cellular ageing: a multicohort study. The lancet. Healthy longevity. 2024;5(7):e454-e463. doi:10.1016/S2666-7568(24)00087-4
Kivimaki M, Frank P, Pentti J, et al. Obesity and risk of diseases associated with hallmarks of cellular ageing: a multicohort study. The lancet. Healthy longevity. 2024;5(7):e454-e463. doi:10.1016/S2666-7568(24)00087-4
Kivimaki M, Frank P, Pentti J, et al. Obesity and risk of diseases associated with hallmarks of cellular ageing: a multicohort study. The lancet. Healthy longevity. 2024;5(7):e454-e463. doi:10.1016/S2666-7568(24)00087-4
Petros BA. Identifying changes in viral fitness using population genetic structure. Proceedings of the National Academy of Sciences of the United States of America. 2024;121(28):e2410274121. doi:10.1073/pnas.2410274121
Gupta AA, Xue W, Harrison DJ, et al. Addition of temsirolimus to chemotherapy in children, adolescents, and young adults with intermediate-risk rhabdomyosarcoma (ARST1431): a randomised, open-label, phase 3 trial from the Children’s Oncology Group. The Lancet. Oncology. 2024;25(7):912-921. doi:10.1016/S1470-2045(24)00255-9
DeSpenza T, Singh A, Allington G, et al. Pathogenic variants in autism gene cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America. 2024;121(27):e2314702121. doi:10.1073/pnas.2314702121