EMERGE

  • DNA helix with a piece cut off and set to the side

    Studies combine genetic testing, electronic health records to find undiagnosed diseases

    Combining genetic testing with information from electronic health records revealed undiagnosed heart rhythm disorders and new conditions associated with inherited cancer gene mutations. Read More

    Apr 28, 2022

  • Genomic analysis visualization. Dna genomes sequencing, deoxyribonucleic acid genetic map and genome sequence analyse. Bioinformatics forensics data or dna radiographic testing vector concept (Genomic analysis visualization

    Probing statin-associated diseases with genetics

    Vanderbilt researchers used genetics tools and biobanks with linked electronic health records to explore the associations between statins and noncardiovascular diseases. Read More

    Jul 12, 2021

  • Vanderbilt University

    VUMC-led network to focus on polygenic risk for common diseases

    With the aid of a $75 million, five-year grant renewal, the Electronic Medical Records and Genomics Network (eMERGE) will venture beyond its current focus on monogenic disease to scoring research participants relative risk for complex heritable diseases such as cardiovascular disease, chronic kidney disease and type 2 diabetes. Read More

    Jul 1, 2020

  • discarded clothing size tags

    Getting the goods on obesity

    Obesity and two post-operative complications linked with it have associated genetic variants in common, suggesting that obesity may be the culprit. Read More

    Nov 19, 2019

  • genetic sequence

    Grants spur effort to add genetic data to EMR

    Vanderbilt University researchers have received two major federal grants — totaling $7.6 million over four years — to support groundbreaking research aimed at making genetic information a routine part of patients’ electronic medical records. Read More

    Sep 10, 2015

  • Deciphering DNA code

    First-ever study uses EMRs to spot new disease associations

    Vanderbilt University Medical Center researchers and co-authors from four other U.S. institutions from the Electronic Medical Records and Genomics (eMERGE) Network are repurposing genetic data and electronic medical records to perform the first large-scale phenome-wide association study (PheWAS), released today in Nature Biotechnology. Read More

    Dec 5, 2013

  • Deciphering DNA code

    Study applies random genotype sets to new disease

    A new study in the American Journal of Human Genetics, led by Vanderbilt researchers Josh Denny, M.D., M.S., and Dana Crawford, Ph.D., takes random volumes of human genotypes and matches them with data siphoned from de-identified medical records and sheds new light on the genetic basis of the common… Read More

    Jan 5, 2012