Kim JY, Song M, Kim MS, et al. An atlas of associations between 14 micronutrients and 22 cancer outcomes: Mendelian randomization analyses. BMC medicine. 2023;21(1):316. doi:10.1186/s12916-023-03018-y
Publications
Babadi M, Fu JM, Lee SK, et al. GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data. Nature genetics. 2023. doi:10.1038/s41588-023-01449-0
Gheinani AH, Kim J, You S, Adam RM. Bioinformatics in urology - molecular characterization of pathophysiology and response to treatment. Nature reviews. Urology. 2023. doi:10.1038/s41585-023-00805-3
Garcia EM, Lue NZ, Liang JK, et al. Base Editor Scanning Reveals Activating Mutations of DNMT3A. ACS chemical biology. 2023. doi:10.1021/acschembio.3c00257
Knudsen MD, Wang K, Wang L, et al. Development and validation of a risk prediction model for post-polypectomy colorectal cancer in the USA: a prospective cohort study. EClinicalMedicine. 2023;62:102139. doi:10.1016/j.eclinm.2023.102139
Ekdahl L, Arrizabalaga AL, Ali Z, Cafaro C, Portilla AL de L, Nilsson B. AliGater: a framework for the development of bioinformatic pipelines for large-scale, high-dimensional cytometry data. Bioinformatics advances. 2023;3(1):vbad103. doi:10.1093/bioadv/vbad103
Surakka I, Wu KH, Hornsby W, et al. Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries. Cell genomics. 2023;3(8):100345. doi:10.1016/j.xgen.2023.100345
Surakka I, Wu KH, Hornsby W, et al. Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries. Cell genomics. 2023;3(8):100345. doi:10.1016/j.xgen.2023.100345
Maury EA, Sherman MA, Genovese G, et al. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent and disruptions. Cell genomics. 2023;3(8):100356. doi:10.1016/j.xgen.2023.100356
Maury EA, Sherman MA, Genovese G, et al. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent and disruptions. Cell genomics. 2023;3(8):100356. doi:10.1016/j.xgen.2023.100356