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- Articles by: Allison Dennis
Allison Dennis's Latest Blog Posts
Allison Dennis | August 11, 2021
Each year since 2018, new Leading Edge Acceleration Projects (LEAP) in Health IT awardees join an entrepreneurial group dedicated to developing and scaling technological breakthroughs. Together, these awardees bring forth solutions to advance research capabilities and improve care delivery. This year is no exception. The University of Texas at Austin (UT Austin) and DARTNet Institute are the newest awardees under ONC’s LEAP in Health IT funding opportunity.Read Full Post.
Allison Dennis | April 21, 2021
Today, ONC is pleased to announce two demonstration sites selected for Sync for Genes Phase 4. Since its launch in 2017, the ONC Sync for Genes project has advanced the standardized sharing of genomic information between laboratories, providers, patients, and researchers. Sync for Genes uses the Health Level 7 (HL7®) International FHIR® standard to enable the electronic sharing of genomic data.Read Full Post.
Allison Dennis | March 2, 2021
Today’s health information ecosystem is broadening in terms of participants and data availability. The data sources that exist to inform clinical and biomedical research are more diverse than ever, drawing from electronic health records (EHRs), genomic tests, recordings from wearable devices, and patient surveys, to name a few. The insights that can be drawn from these require effective data collection, aggregation, and sharing in addition to health IT infrastructure capable of supporting research goals. To address some of these requirements,Read Full Post.
Allison Dennis | January 26, 2021
Does the neighborhood I live in affect my health? How am I going to be able to see the specialist without a car? Can I share blood pressure and blood sugar readings I take at home with my doctor so she can monitor how I’m doing? These critical questions have helped to drive precision medicine research as well as improving care management and coordination.Read Full Post.
Allison Dennis | January 7, 2021
The use of genetic testing is becoming increasingly routine in patient care. For example, tests are available to check newborns for genetic disorders, screen would-be parents for carrier status, inform cancer care, and evaluate potential pharmacogenetic associations. However, the laboratories that perform these tests face many challenges that keep them from being able to return clinical genomic results in a standardized way and fully leverage a patient’s electronic health record. This also affects healthcare professionals’ ability to deliver precision medicine and conduct precision medicine research.Read Full Post.