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  • Single-cell RNA sequencing distinctly characterizes the wide heterogeneity in pediatric mixed phenotype acute leukemia
  • Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity
  • A community-driven resource for genomic epidemiology and antimicrobial resistance prediction of Neisseria gonorrhoeae at Pathogenwatch
  • Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes
  • Advancing precision public health using human genomics: examples from the field and future research opportunities
  • Highly elevated polygenic risk scores are better predictors of myocardial infarction risk early in life than later
  • Multi-tissue neocortical transcriptome-wide association study implicates 8 genes across 6 genomic loci in Alzheimer’s disease
  • Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age
  • Disease-specific regulation of gene expression in a comparative analysis of juvenile idiopathic arthritis and inflammatory bowel disease
  • BALDR: a computational pipeline for paired heavy and light chain immunoglobulin reconstruction in single-cell RNA-seq data