Murray H. Brilliant
University of Wisconsin–Madison(US)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Retinal Diseases and Treatments, Glaucoma and retinal disorders, Genomics and Rare Diseases, Ethics in Clinical Research
Most-Cited Works
- → Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data(2013)1,111 cited
- → The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future(2013)734 cited
- → Implementing genomic medicine in the clinic: the future is here(2013)563 cited
- → Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries(2021)466 cited
- → Comparison of RNA-seq and microarray-based models for clinical endpoint prediction(2015)426 cited
- → PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study(2016)384 cited
- → Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between(2014)375 cited
- → The All of Us Research Program: Data quality, utility, and diversity(2022)314 cited
- → Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US(2017)253 cited
- → Design and Anticipated Outcomes of the eMERGE-PGx Project: A Multicenter Pilot for Preemptive Pharmacogenomics in Electronic Health Record Systems(2014)242 cited