Genome Medicine
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Publication Venue For
- Correction to: Family history assessment significantly enhances delivery of precision medicine in the genomics era.. 13:109. 2021
- The host transcriptional response to Candidemia is dominated by neutrophil activation and heme biosynthesis and supports novel diagnostic approaches.. 13:108. 2021
- An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility.. 13:83. 2021
- Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci.. 13:74. 2021
- Family history assessment significantly enhances delivery of precision medicine in the genomics era.. 13:3. 2021
- DNA methylation and body mass index from birth to adolescence: meta-analyses of epigenome-wide association studies.. 12:105. 2020
- Wnt-regulated lncRNA discovery enhanced by in vivo identification and CRISPRi functional validation.. 12:89. 2020
- A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder.. 9:99. 2017
- Breathing new life into an old target: pulmonary disease drugs for Parkinson's disease therapy.. 9:88. 2017
- Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits.. 9:29. 2017
- Microbiomic differences in tumor and paired-normal tissue in head and neck squamous cell carcinomas.. 9:14. 2017
- Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance.. 7:98. 2015
- How behavioral economics can help to avoid 'The last mile problem' in whole genome sequencing.. 7:3. 2015
- Mutation signatures implicate aristolochic acid in bladder cancer development 2015
- Mutation signatures implicate aristolochic acid in bladder cancer development.. 7:38. 2015
- Patient engagement as a risk factor in personalized health care: A systematic review of the literature on chronic disease. 6. 2014
- An integrated transcriptome and expressed variant analysis of sepsis survival and death.. 6:111. 2014
- Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding.. 6:58. 2014
- Mutation signatures of carcinogen exposure: genome-wide detection and new opportunities for cancer prevention.. 6:24. 2014
- Patient engagement as a risk factor in personalized health care: a systematic review of the literature on chronic disease.. 6:16. 2014
- Incremental value of rare genetic variants for the prediction of multifactorial diseases.. 5:76. 2013
- H3K4me3 inversely correlates with DNA methylation at a large class of non-CpG-island-containing start sites.. 4:47. 2012