ArticleJournal of the American Medical Informatics Association : JAMIA2018
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
Article in Journal of the American Medical Informatics Association : JAMIA, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
18 citing papers in PubMed.
- Advancing the science of genomic learning healthcare systems.Learning health systems · 2025Article
- Pharmacogenomic testing implementation: Tertiary care center experience and results of a pilot of 512 patients.Genetics in medicine open · 2025Article
- Paving the path for implementation of clinical genomic sequencing globally: Are we ready?Health affairs scholar · 2024Article
- Tracking updates in clinical databases increases efficiency for variant reanalysis.Genetics in medicine open · 2024Article
- Imaging genomics: data fusion in uncovering disease heritability.Trends in molecular medicine · 2023Review
- The roles of the US National Library of Medicine and Donald A.B. Lindberg in revolutionizing biomedical and health informatics.Journal of the American Medical Informatics Association : JAMIA · 2021Article
- Neptune: an environment for the delivery of genomic medicine.Genetics in medicine : official journal of the American College of Medical Genetics · 2021Article
- Facilitating Genetics Aware Clinical Decision Support: Putting the eMERGE Infrastructure into Practice.ACI open · 2021Article
- Genomic considerations for FHIR®; eMERGE implementation lessons.Journal of biomedical informatics · 2021Article
- The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System.JMIR research protocols · 2021Article
- Lessons learned from the eMERGE Network: balancing genomics in discovery and practice.HGG advances · 2021Review
- An electronic health record (EHR) log analysis shows limited clinician engagement with unsolicited genetic test results.JAMIA open · 2021Article
- Solutions for Unexpected Challenges Encountered when Integrating Research Genomics Results into the EHR.ACI open · 2020Article
- Calling on Primary Care to Prevent BRCA-Related Cancers.Journal of general internal medicine · 2020Article
- Integrating pharmacogenomics into the electronic health record by implementing genomic indicators.Journal of the American Medical Informatics Association : JAMIA · 2020Article
- ARBoR: an identity and security solution for clinical reporting.Journal of the American Medical Informatics Association : JAMIA · 2019Article
- Pathway analysis of genomic pathology tests for prognostic cancer subtyping.Journal of biomedical informatics · 2019Article
- Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.American journal of human genetics · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
25 authors.
Funding
Abstract
The eMERGE Network is establishing methods for electronic transmittal of patient genetic test results from laboratories to healthcare providers across organizational boundaries. We surveyed the capabilities and needs of different network participants, established a common transfer format, and implemented transfer mechanisms based on this format. The interfaces we created are examples of the connectivity that must be instantiated before electronic genetic and genomic clinical decision support can be effectively built at the point of care. This work serves as a case example for both standards bodies and other organizations working to build the infrastructure required to provide better electronic clinical decision support for clinicians.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.