Integration of genomics into the electronic health record: mapping terra incognita.

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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

1. Machine Learning and Pharmacogenomics at the Time of Precision Psychiatry.Current neuropharmacology · 2023
   Pooled it
2. Service Outcomes for Germline Test Delivery for Patients With Metastatic Prostate Cancer.JAMA network open · 2026
   Article
3. New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects.Journal of Taibah University Medical Sciences · 2023
   Article
4. Leveraging a pharmacogenomics knowledgebase to formulate a drug response phenotype terminology for genomic medicine.Bioinformatics (Oxford, England) · 2022
   Article
5. Deep learning in pharmacogenomics: from gene regulation to patient stratification.Pharmacogenomics · 2018
   Review
6. Mouse Injury Model of Polytrauma and Shock.Methods in molecular biology (Clifton, N.J.) · 2018
   Review
7. Assessing the readiness of precision medicine interoperabilty: An exploratory study of the National Institutes of Health genetic testing registry.Journal of innovation in health informatics · 2017
   Article
8. -Omic and Electronic Health Record Big Data Analytics for Precision Medicine.IEEE transactions on bio-medical engineering · 2017
   Review
9. Large-Scale Discovery of Disease-Disease and Disease-Gene Associations.Scientific reports · 2016
   Article
10. Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).Journal of the American Medical Informatics Association : JAMIA · 2016
    Article
11. Integrating "big data" into surgical practice.Surgery · 2016
    Review
12. The future of murine sepsis and trauma research models.Journal of leukocyte biology · 2015
    Review
13. CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.Journal of the American Medical Informatics Association : JAMIA · 2015
    Article
14. Contemporary Considerations for Constructing a Genetic Risk Score: An Empirical Approach.Genetic epidemiology · 2015
    Article
15. Cancer biomarker discovery and validation.Translational cancer research · 2015
    Article
16. Supporting interoperability of genetic data with LOINC.Journal of the American Medical Informatics Association : JAMIA · 2015
    Article
17. The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2014
    Article
18. Return of results in the genomic medicine projects of the eMERGE network.Frontiers in genetics · 2014
    Article
19. Making Personalized Health Care Even More Personalized: Insights From Activities of the IOM Genomics Roundtable.Annals of family medicine
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

2 authors.

Funding

Abstract

PubMed holds no abstract for this paper.

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