ArticleScience translational medicine2014
Biobanks and electronic medical records: enabling cost-effective research.
Article in Science translational medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05277116 (The Electronic Medical Records and GEnomics), which is not on this map. Cited by 98 papers, 2 of them syntheses that pooled it.
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.
The Electronic Medical Records and GEnomics (eMERGE) Network Genomic Risk Assessment
Who cites it
98 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- A systematic literature review of machine learning in online personal health data.Journal of the American Medical Informatics Association : JAMIA · 2019Pooled it
- Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.The Lancet. Respiratory medicine · 2019Pooled it
- Inclusion bias affects common variant discovery and replication in a health-system linked biobank.American journal of human genetics · 2026Article
- Impact of CYP2D6 Metabolizer Status on Ondansetron Efficacy in Early Pregnancy Induced Nausea and Vomiting: A Case Control Study.Clinical and translational science · 2026Article
- Expanding scope of genetic studies in the era of biobanks.Human molecular genetics · 2025Article
- Pharmacogenetics: Opportunities for theAnnual review of pharmacology and toxicology · 2025Review
- Artificial intelligence-assisted automated heart failure detection and classification from electronic health records.ESC heart failure · 2024Article
- Genetics and precision genomics approaches to pulmonary hypertension.The European respiratory journal · 2024Review
- Using electronic health records for clinical pharmacology research: Challenges and considerations.Clinical and translational science · 2024Review
- Phenomewide Association Study of Health Outcomes Associated With the Genetic Correlates of 25 Hydroxyvitamin D Concentration and Vitamin D Binding Protein Concentration.Twin research and human genetics : the official journal of the International Society for Twin Studies · 2024Article
- Composite CYP3A (CYP3A4 and CYP3A5) phenotypes and influence on tacrolimus dose adjusted concentrations in adult heart transplant recipients.The pharmacogenomics journal · 2024Article
- Revolutionizing Cancer Research: The Impact of Artificial Intelligence in Digital Biobanking.Journal of personalized medicine · 2023Review
- Pharmacogenomics: current status and future perspectives.Nature reviews. Genetics · 2023Review
- Evaluating resources composing the PheMAP knowledge base to enhance high-throughput phenotyping.Journal of the American Medical Informatics Association : JAMIA · 2023Article
- Is there a civic duty to support medical AI development by sharing electronic health records?BMC medical ethics · 2022Article
- Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease.Cell genomics · 2022Article
- Article
- Novel Analysis Methods to Mine Immune-Mediated Phenotypes and Find Genetic Variation Within the Electronic Health Record (Roadmap for Phenotype to Genotype: Immunogenomics).The journal of allergy and clinical immunology. In practice · 2022Review
- Influence of CYP2D6 genetic variation on adverse events with propafenone in the pediatric and young adult population.Clinical and translational science · 2022Article
- Accuracy of identifying hospital acquired venous thromboembolism by administrative coding: implications for big data and machine learning research.Journal of clinical monitoring and computing · 2022Article
38 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
16 authors.
Funding
Abstract
The use of electronic medical record data linked to biological specimens in health care settings is expected to enable cost-effective and rapid genomic analyses. Here, we present a model that highlights potential advantages for genomic discovery and describe the operational infrastructure that facilitated multiple simultaneous discovery efforts.
Indexed as
Identifiers
What OpenQuestion holds
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.