Maamari DJ, Abou-Karam R, Fahed AC. Polygenic Risk Scores in Human Disease. Clinical chemistry. 2025;71(1):69-76. doi:10.1093/clinchem/hvae190
Publications
Rehm HL. Overcoming Barriers to Genomic Medicine Implementation. Clinical chemistry. 2025;71(1):4-9. doi:10.1093/clinchem/hvae147
Giersch ABS, Morton CC. Newborn Screening for Deafness/Hard of Hearing in the Genomic Era. Clinical chemistry. 2025;71(1):54-60. doi:10.1093/clinchem/hvae193
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
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