Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper.
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Ethical and practical issues associated with aggregating databasesThe SAIL Databank: building a national architecture for e-health research and evaluationMaking big data useful for health care: a summary of the inaugural MIT critical data conferenceA systematic review of barriers to data sharing in public healthBuilding a robust, scalable and standards-driven infrastructure for secondary use of EHR data: the SHARPn projectThe future state of clinical data capture and documentation: a report from AMIA's 2011 Policy MeetingDesigning a patient-centered user interface for access decisions about EHR data: implications from patient interviewsUsing patient lists to add value to integrated data repositoriesEstablishing the role of honest broker: bridging the gap between protecting personal health data and clinical research efficiencyOverview of the American Society for Radiation Oncology-National Institutes of Health-American Association of Physicists in Medicine Workshop 2015: Exploring Opportunities for Radiation Oncology in the Era of Big DataAn integrated, ontology-driven approach to constructing observational databases for researchSecondary use of clinical data: the Vanderbilt approachBeyond information retrieval and electronic health record use: competencies in clinical informatics for medical educationQuantifying the Correctness, Computational Complexity, and Security of Privacy-Preserving String Comparators for Record LinkageGrid-enabled measures: using Science 2.0 to standardize measures and share dataConsortium for oral health-related informatics: improving dental research, education, and treatmentNever too old for anonymity: a statistical standard for demographic data sharing via the HIPAA Privacy RuleEvaluating re-identification risks with respect to the HIPAA privacy rulecaTIES: a grid based system for coding and retrieval of surgical pathology reports and tissue specimens in support of translational researchThe population health record: concepts, definition, design, and implementationPeople and organizational issues in research systems implementationTowards a data sharing culture: recommendations for leadership from academic health centersIdentifying data sharing in biomedical literatureMethods and dimensions of electronic health record data quality assessment: enabling reuse for clinical researchOntology-based data integration between clinical and research systemsUsing Informatics to Improve the Care of Patients Susceptible to Malignant Hyperthermia.Acceptability of a personally controlled health record in a community-based setting: implications for policy and designAdjusting for unmeasured confounding in non-randomised longitudinal studies: a methodological review.Review and evaluation of electronic health records-driven phenotype algorithm authoring tools for clinical and translational research.Reuse of clinical data.Health data use, stewardship, and governance: ongoing gaps and challenges: a report from AMIA's 2012 Health Policy Meeting.Data for cancer comparative effectiveness research: past, present, and future potential.A framework for understanding cancer comparative effectiveness research data needsPROTEMPA: a method for specifying and identifying temporal sequences in retrospective data for patient selection.Transparent reporting of data quality in distributed data networks.Orchestrating differential data access for translational research: a pilot implementation.HIS-based Kaplan-Meier plots--a single source approach for documenting and reusing routine survival information.Barriers to retrieving patient information from electronic health record data: failure analysis from the TREC Medical Records Track.Evaluation of data completeness in the electronic health record for the purpose of patient recruitment into clinical trials: a retrospective analysis of element presence.Caveats for the use of operational electronic health record data in comparative effectiveness research.
P2860
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P2860
Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper.
description
2006 nî lūn-bûn
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2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հոտեմբերին հրատարակված գիտական հոդված
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2006年の論文
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2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Toward a national framework fo ...... atics Association White Paper.
@ast
Toward a national framework fo ...... atics Association White Paper.
@en
type
label
Toward a national framework fo ...... atics Association White Paper.
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Toward a national framework fo ...... atics Association White Paper.
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prefLabel
Toward a national framework fo ...... atics Association White Paper.
@ast
Toward a national framework fo ...... atics Association White Paper.
@en
P2093
P356
P1476
Toward a national framework fo ...... atics Association White Paper.
@en
P2093
Charles Safran
Don E Detmer
Expert Panel
Meryl Bloomrosen
Paul C Tang
Steven Labkoff
Suzanne Markel-Fox
W Edward Hammond
P356
10.1197/JAMIA.M2273
P577
2006-10-31T00:00:00Z