Chalitsios C V, Markozannes G, Papagiannopoulos C, et al. Waist Circumference, a Body Shape Index, and Molecular Subtypes of Colorectal Cancer: A Pooled Analysis of Four Cohort Studies. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2025;34(4):568-577. doi:10.1158/1055-9965.EPI-24-1534
Publications
Kreienkamp RJ, Deutsch AJ, Huerta-Chagoya A, et al. Type 1 Diabetes Polygenic Scores Improve Diagnostic Accuracy in Pediatric Diabetes Care. medRxiv : the preprint server for health sciences. 2025. doi:10.1101/2025.03.06.25323229
Perugino CA, Liu H, Feldman J, et al. Two distinct durable human class-switched memory B cell populations are induced by vaccination and infection. Cell reports. 2025;44(4):115472. doi:10.1016/j.celrep.2025.115472
Kany S, Rämö JT, Playford D, et al. New Threshold for Defining Mild Aortic Stenosis Derived From Velocity-Encoded MRI in 60,000 Individuals. Journal of the American College of Cardiology. 2025;85(13):1387-1399. doi:10.1016/j.jacc.2025.01.035
Waterbury AL, Caroli J, Zhang O, et al. Covalent adduct Grob fragmentation underlies LSD1 demethylase-specific inhibitor mechanism of action and resistance. Nature communications. 2025;16(1):3156. doi:10.1038/s41467-025-57477-3
Schuermans A, Honigberg MC. Clonal haematopoiesis in cardiovascular disease: prognostic role and novel therapeutic target. Nature reviews. Cardiology. 2025. doi:10.1038/s41569-025-01148-9
Bruxel EM, Rovaris DL, Belangero SI, et al. Psychiatric genetics in the diverse landscape of Latin American populations. Nature genetics. 2025. doi:10.1038/s41588-025-02127-z
Daya FA, Mandigo T, Ober L, et al. Identifying novel links between cardiovascular disease and insomnia by Drosophila modeling of genes from a pleiotropic GWAS locus. Disease models & mechanisms. 2025. doi:10.1242/dmm.052139
D’Gama AM, Phillips HW, Wang Y, et al. Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants. Brain communications. 2025;7(2):fcaf113. doi:10.1093/braincomms/fcaf113
Foley R, Bolduc V, Guirguis F, et al. Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T. Brain : a journal of neurology. 2025. doi:10.1093/brain/awaf116