Dalin S, Webster S, Sugawara N, et al. Mutations and structural variants arising during double-strand break repair. Proceedings of the National Academy of Sciences of the United States of America. 2026;123(6):e2504584123. doi:10.1073/pnas.2504584123
Publications
Lynce F, Graham N, Kochupurakkal BS, et al. A Phase Ib Study of Sapacitabine and Olaparib in Patients with BRCA1/2-Mutated Metastatic Breast Cancer. Clinical cancer research : an official journal of the American Association for Cancer Research. 2026;32(3):489-500. doi:10.1158/1078-0432.CCR-25-0571
Li MM, Reis BY, Rodman A, et al. Scaling medical AI across clinical contexts. Nature medicine. 2026. doi:10.1038/s41591-025-04184-7
Strom NI, Verhulst B, Bacanu SA, et al. Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling. Nature genetics. 2026. doi:10.1038/s41588-025-02485-8
Cooper E, Posner DA, Lee CYC, et al. Childhood brain tumors instruct cranial hematopoiesis and immunotolerance. Nature genetics. 2026. doi:10.1038/s41588-025-02499-2
Schwabl P, Amaya-Romero JE, Kelley KA, et al. SIMPLseq: a high-sensitivity Plasmodium falciparum genotyping and PCR contamination tracking tool. Malaria journal. 2026. doi:10.1186/s12936-026-05796-1
Lim SH, An M, Heo YJ, et al. Distinct Spatially Resolved Tumor Microenvironment Trajectories Define Benefit from Ramucirumab plus Pembrolizumab in Refractory PD-L1+ Gastric Cancer. Cancer immunology research. 2026;14(2):307-317. doi:10.1158/2326-6066.CIR-25-0625
PMCID
PMC12767546
Pini V, Catapano F, Bonaccorso R, Weisburd B, Previtali SC, Muntoni F. Muscle transcriptome profiling reveals novel molecular pathways and biomarkers in laminin-α2 deficient patients. Acta neuropathologica communications. 2026. doi:10.1186/s40478-026-02227-9
Tchio C, Maher M, Moth C, et al. Circadian Ser107Pro variant bridges difficulty awakening in the morning and adiposity. iScience. 2026;29(2):114587. doi:10.1016/j.isci.2025.114587
PMCID
PMC12860998
Liu E, Zhang J, Uhler C. Learning genetic perturbation effects with variational causal inference. PLoS computational biology. 2026;22(2):e1013194. doi:10.1371/journal.pcbi.1013194