Genome Medicine View Homepage


Ontology type: schema:Periodical      Open Access: True


Journal Info

START YEAR

2009

PUBLISHER

BioMed Central

LANGUAGE

en

HOMEPAGE

http://genomemedicine.biomedcentral.com

Recent publications latest 20 shown

  • 2019-12 De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
  • 2019-12 A decade of Genome Medicine: toward precision medicine
  • 2019-12 Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium
  • 2019-12 Translating insights into tumor evolution to clinical practice: promises and challenges
  • 2019-12 Reconstruction of full-length circular RNAs enables isoform-level quantification
  • 2019-12 From genome integrity to cancer
  • 2019-12 Prioritizing putative influential genes in cardiovascular disease susceptibility by applying tissue-specific Mendelian randomization
  • 2019-12 Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
  • 2019-12 Ten years of Genome Medicine
  • 2019-12 Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
  • 2019-12 Translating genomic medicine to the clinic: challenges and opportunities
  • 2019-12 Correction to: NSAID use and somatic exomic mutations in Barrett’s esophagus
  • 2019-12 Encircling the regions of the pharmacogenomic landscape that determine drug response
  • 2019-12 Single-cell analysis reveals congruence between kidney organoids and human fetal kidney
  • 2019-12 Next Generation-Targeted Amplicon Sequencing (NG-TAS): an optimised protocol and computational pipeline for cost-effective profiling of circulating tumour DNA
  • 2019-12 BAP1 haploinsufficiency predicts a distinct immunogenic class of malignant peritoneal mesothelioma
  • 2019-12 Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
  • 2019-12 Circular RNAs as promising biomarkers in cancer: detection, function, and beyond
  • 2019-12 Loss of BAP1 as a candidate predictive biomarker for immunotherapy of mesothelioma
  • 2019-12 Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data
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