@article{3a49f84546904aa28b3e3df8c8a2272d,
title = "Genomic information for clinicians in the electronic health record: Lessons learned from the clinical genome resource project and the electronic medical records and genomics network",
abstract = "Genomic knowledge is being translated into clinical care. To fully realize the value, it is critical to place credible information in the hands of clinicians in time to support clinical decision making. The electronic health record is an essential component of clinician workflow. Utilizing the electronic health record to present information to support the use of genomic medicine in clinical care to improve outcomes represents a tremendous opportunity. However, there are numerous barriers that prevent the effective use of the electronic health record for this purpose. The electronic health record working groups of the Electronic Medical Records and Genomics (eMERGE) Network and the Clinical Genome Resource (ClinGen) project, along with other groups, have been defining these barriers, to allow the development of solutions that can be tested using implementation pilots. In this paper, we present “lessons learned” from these efforts to inform future efforts leading to the development of effective and sustainable solutions that will support the realization of genomic medicine.",
keywords = "Clinical decision support, Education, Electronic health record, Genomics, Implementation, Infobutton, Interoperability, Knowledge synthesis",
author = "Williams, {Marc S.} and Taylor, {Casey Overby} and Walton, {Nephi A.} and Goehringer, {Scott R.} and Samuel Aronson and Freimuth, {Robert R.} and Rasmussen, {Luke V.} and Hall, {Eric S.} and Prows, {Cynthia A.} and Chung, {Wendy K.} and Alexander Fedotov and Jordan Nestor and Chunhua Weng and Rowley, {Robb K.} and Wiesner, {Georgia L.} and Jarvik, {Gail P.} and Fiol, {Guilherme Del}",
note = "Funding Information: Brigham and Women{\textquoteright}s Hospital: U01HG8685 (eMERGE); Cincinnati Children{\textquoteright}s Hospital Medical Center: U01HG8666 (eMERGE); Columbia University: U01HG008680 (eMERGE); Geisinger Clinic: U01HG8679 (eMERGE) and U41HG009650 (ClinGen); Group Health Cooperative/University of Washington: U01HG8657 (eMERGE); Mayo Clinic: U01HG063798 (eMERGE) and U41HG068345 (ClinGen); Northwestern University: U01HG8673 (eMERGE); Partners HealthCare/Broad Institute: U01HG8676 (eMERGE); Vanderbilt University Medical Center: U01HG8672 (eMERGE). The authors wish to recognize the contributions of other members of the eMERGE network who have contributed to work reported in this paper. Dr. Hakon Hakonarson (Children{\textquoteright}s Hospital of Philadelphia), Sheethal Jose (National Human Genome Research Institute), Dr. Josh Peterson and Dr. Ellen Wright Clayton (Vanderbilt University). Funding Information: The work was done in two large research projects funded by the National Human Genome Research Institute (NHGRI). Publisher Copyright: {\textcopyright} 2019 Williams, Taylor, Walton, Goehringer, Aronson, Freimuth, Rasmussen, Hall, Prows, Chung, Fedotov, Nestor, Weng, Rowley, Wiesner, Jarvik and Del Fiol.",
year = "2019",
doi = "10.3389/fgene.2019.01059",
language = "English (US)",
volume = "10",
journal = "Frontiers in Genetics",
issn = "1664-8021",
publisher = "Frontiers Media S. A.",
number = "OCT",
}