Adams S, Trocki OM, Miller C, et al. Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions. Clinical chemistry. 2025;71(1):129-140. doi:10.1093/clinchem/hvae189
Publications
van Dijk LR, Manson AL, Earl AM, Garimella K V, Abeel T. Fast exact gap-affine partial order alignment with POASTA. Bioinformatics (Oxford, England). 2025. doi:10.1093/bioinformatics/btae757
van Dijk LR, Manson AL, Earl AM, Garimella K V, Abeel T. Fast exact gap-affine partial order alignment with POASTA. Bioinformatics (Oxford, England). 2025. doi:10.1093/bioinformatics/btae757
Frazier ZJ, Kilic S, Osika H, et al. Novel Phenotypes and Genotype-Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome. Clinical genetics. 2025. doi:10.1111/cge.14697
Mundy J, Hall ASM, Agerbo E, et al. Genetic Confounding of the Association Between Age at First Hormonal Contraception and Depression. Acta psychiatrica Scandinavica. 2025. doi:10.1111/acps.13774
Mishra A, Huang SB, Dubash T, et al. Tumor cell-based liquid biopsy using high-throughput microfluidic enrichment of entire leukapheresis product. Nature communications. 2025;16(1):32. doi:10.1038/s41467-024-55140-x
Strober BJ, Zhang MJ, Amariuta T, Rossen J, Price AL. Fine-mapping causal tissues and genes at disease-associated loci. Nature genetics. 2025. doi:10.1038/s41588-024-01994-2
Kim S, Ko H, Myung W, et al. Association between genetically predicted leisure and social activities and cardiovascular disease and other health outcomes. Nature cardiovascular research. 2025. doi:10.1038/s44161-024-00581-2
Kim S, Ko H, Myung W, et al. Association between genetically predicted leisure and social activities and cardiovascular disease and other health outcomes. Nature cardiovascular research. 2025. doi:10.1038/s44161-024-00581-2
Weng LC, Rämö JT, Jurgens SJ, et al. The impact of common and rare genetic variants on bradyarrhythmia development. Nature genetics. 2025. doi:10.1038/s41588-024-01978-2