Daenekas B, Pérez E, Boniolo F, et al. Conumee 2.0: Enhanced copy-number variation analysis from DNA methylation arrays for humans and mice. Bioinformatics (Oxford, England). 2024. doi:10.1093/bioinformatics/btae029
Publications
Mei H, Simino J, Li L, et al. Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance. Alzheimer’s research & therapy. 2024;16(1):14. doi:10.1186/s13195-023-01376-6
Kang J, Park J, Lee M, et al. National Trends and Prevalence of Atopic Dermatitis and Pandemic-Related Factors among Korean Adults, 2007-2021. International archives of allergy and immunology. 2024:1-14. doi:10.1159/000535666
Hosang GM, Shakoor S, King N, et al. Interplay between polygenic risk for mood disorders and stressful life events in bipolar disorder. Journal of affective disorders. 2024. doi:10.1016/j.jad.2024.01.167
Nystuen KL, McNamee SM, Akula M, Holton KM, DeAngelis MM, Haider NB. Alzheimer’s Disease: Models and Molecular Mechanisms Informing Disease and Treatments. Bioengineering (Basel, Switzerland). 2024;11(1). doi:10.3390/bioengineering11010045
Schirmer M, Stražar M, Avila-Pacheco J, et al. Linking microbial genes to plasma and stool metabolites uncovers host-microbial interactions underlying ulcerative colitis disease course. Cell host & microbe. 2024. doi:10.1016/j.chom.2023.12.013
Meisel JD, Miranda M, Skinner OS, et al. Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism. Cell. 2024. doi:10.1016/j.cell.2023.12.010
Tegtmeyer M, Arora J, Asgari S, et al. High-dimensional phenotyping to define the genetic basis of cellular morphology. Nature communications. 2024;15(1):347. doi:10.1038/s41467-023-44045-w
Taraszka K, Groha S, King D, et al. A comprehensive analysis of clinical and polygenic germline influences on somatic mutational burden. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2023.12.010
Artomov M, Loboda AA, Artyomov MN, Daly MJ. Public platform with 39,472 exome control samples enables association studies without genotype sharing. Nature genetics. 2024. doi:10.1038/s41588-023-01637-y