Journal of the American Medical Informatics Association : JAMIA
Journal
Overview
publication venue for
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Corrigendum to: Practice and market factors associated with provider volume of health information exchange.
2021
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Semi-supervised learning from small annotated data and large unlabeled data for fine-grained Participants, Intervention, Comparison, and Outcomes entity recognition.
2025
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A machine learning framework to adjust for learning effects in medical device safety evaluation.
2024
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Extracting social support and social isolation information from clinical psychiatry notes: comparing a rule-based natural language processing system and a large language model.
2024
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Toward a responsible future: recommendations for AI-enabled clinical decision support.
2024
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Model-based estimation of individual-level social determinants of health and its applications in All of Us.
2024
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Understanding enterprise data warehouses to support clinical and translational research: impact, sustainability, demand management, and accessibility.
2024
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Strengthening the use of artificial intelligence within healthcare delivery organizations: balancing regulatory compliance and patient safety.
2024
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Preparing for the bedside-optimizing a postpartum depression risk prediction model for clinical implementation in a health system.
2024
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A span-based model for extracting overlapping PICO entities from RCT publications.
2024
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Bridging the digital health divide-patient experiences with mobile integrated health and facilitated telehealth by community-level indicators of health disparity.
2024
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Confidence Score: A Data-Driven Measure for Inclusive Systematic Reviews Considering Unpublished Preprints.
2023
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A method to automate the discharge summary hospital course for neurology patients..
30.
2023
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Visualizing machine learning-based predictions of postpartum depression risk for lay audiences.
2023
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Do you want to promote recall, perceptions, or behavior? The best data visualization depends on the communication goal.
2023
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Impact of notification policy on patient-before-clinician review of immediately released test results.
2023
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De-black-boxing health AI: demonstrating reproducible machine learning computable phenotypes using the N3C-RECOVER Long COVID model in the All of Us data repository.
2023
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An NLP approach to identify SDoH-related circumstance and suicide crisis from death investigation narratives.
2023
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EvidenceMap: a three-level knowledge representation for medical evidence computation and comprehension.
2023
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Examining medication ordering errors using AHRQ network of patient safety databases.
2023
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Characterizing variability of electronic health record-driven phenotype definitions.
2022
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Assessing the impact of privacy-preserving record linkage on record overlap and patient demographic and clinical characteristics in PCORnet®, the National Patient-Centered Clinical Research Network.
2022
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Engaging the next generation of physician-informaticians through early exposure to the field: successes and challenges associated with starting a novel clinical informatics interest group.
2022
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Building trust in research through information and intent transparency with health information: representative cross-sectional survey of 502 US adults..
29.
2022
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Using CDS Hooks to increase SMART on FHIR app utilization: a cluster-randomized trial..
29.
2022
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Design and validation of a FHIR-based EHR-driven phenotyping toolbox.
2022
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An architecture for research computing in health to support clinical and translational investigators with electronic patient data..
29.
2022
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Synergies between centralized and federated approaches to data quality: a report from the national COVID cohort collaborative..
29.
2022
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Understanding enterprise data warehouses to support clinical and translational research: enterprise information technology relationships, data governance, workforce, and cloud computing..
29.
2022
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Improving suicide risk prediction via targeted data fusion: proof of concept using medical claims data..
29.
2022
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Design and evaluation of a Women in American Medical Informatics Association (AMIA) leadership program..
29.
2021
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Trust in AI: why we should be designing for APPROPRIATE reliance..
29.
2021
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Deep significance clustering: a novel approach for identifying risk-stratified and predictive patient subgroups..
28.
2021
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Guidance for publishing qualitative research in informatics..
28.
2021
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Practice and market factors associated with provider volume of health information exchange..
28.
2021
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Multimodal, multitask, multiattention (M3) deep learning detection of reticular pseudodrusen: Toward automated and accessible classification of age-related macular degeneration..
28.
2021
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Clinical informatics during the COVID-19 pandemic: Lessons learned and implications for emergency department and inpatient operations..
28.
2021
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The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment..
28.
2021
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Trends in user-initiated health information exchange in the inpatient, outpatient, and emergency settings..
28.
2021
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Understanding enterprise data warehouses to support clinical and translational research..
27.
2020
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"How did you get to this number?" Stakeholder needs for implementing predictive analytics: a pre-implementation qualitative study..
27.
2020
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Visual analogies, not graphs, increase patients' comprehension of changes in their health status..
27.
2020
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The complementary nature of query-based and directed health information exchange in primary care practice..
27.
2020
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ML-Net: multi-label classification of biomedical texts with deep neural networks..
26.
2019
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Health systems' use of enterprise health information exchange vs single electronic health record vendor environments and unplanned readmissions..
26.
2019
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Structured override reasons for drug-drug interaction alerts in electronic health records..
26.
2019
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Challenges with quality of race and ethnicity data in observational databases..
26.
2019
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Interventions to increase patient portal use in vulnerable populations: a systematic review..
26.
2019
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Underserved populations with missing race ethnicity data differ significantly from those with structured race/ethnicity documentation..
26.
2019
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Evaluating the effect of data standardization and validation on patient matching accuracy..
26.
2019
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Integrity of clinical information in computerized order requisitions for diagnostic imaging..
25.
2018
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Should parents see their teen's medical record? Asking about the effect on adolescent-doctor communication changes attitudes..
25.
2018
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A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments..
25.
2018
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Developing and maintaining clinical decision support using clinical knowledge and machine learning: the case of order sets..
25.
2018
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Efficacy and unintended consequences of hard-stop alerts in electronic health record systems: a systematic review..
25.
2018
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Hospitals' adoption of intra-system information exchange is negatively associated with inter-system information exchange..
25.
2018
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The benefits of health information exchange: an updated systematic review..
25.
2018
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Evaluation of a recommender app for apps for the treatment of depression and anxiety: an analysis of longitudinal user engagement..
25.
2018
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Variability in adolescent portal privacy features: how the unique privacy needs of the adolescent patient create a complex decision-making process..
25.
2018
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Assessing the capacity of social determinants of health data to augment predictive models identifying patients in need of wraparound social services..
25.
2018
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Effect of health information exchange on recognition of medication discrepancies is interrupted when data charges are introduced: results of a cluster-randomized controlled trial..
24.
2017
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The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations..
24.
2017
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Hospitalization event notifications and reductions in readmissions of Medicare fee-for-service beneficiaries in the Bronx, New York..
24.
2017
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Variation in high-priority drug-drug interaction alerts across institutions and electronic health records..
24.
2017
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The organization and content of informatics doctoral dissertations..
23.
2016
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Health information exchange in the wild: the association between organizational capability and perceived utility of clinical event notifications in ambulatory and community care..
24.
2016
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PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability..
23.
2016
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Automatic detection of social rhythms in bipolar disorder..
23.
2016
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Effects of an e-Prescribing interface redesign on rates of generic drug prescribing: exploiting default options..
23.
2016
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Modeling information flows in clinical decision support: key insights for enhancing system effectiveness..
23.
2016
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Desiderata for computable representations of electronic health records-driven phenotype algorithms..
22.
2015
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Sometimes more is more: iterative participatory design of infographics for engagement of community members with varying levels of health literacy..
23.
2015
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Center of excellence for mobile sensor data-to-knowledge (MD2K)..
22.
2015
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Associations between healthcare quality and use of electronic health record functions in ambulatory care..
22.
2015
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A needs assessment of health information technology for improving care coordination in three leading patient-centered medical homes..
22.
2015
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Electronic health records and health care quality over time in a federally qualified health center..
22.
2015
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The potential for community-based health information exchange systems to reduce hospital readmissions..
22.
2014
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How is the electronic health record being used? Use of EHR data to assess physician-level variability in technology use..
21.
2014
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Changing the research landscape: the New York City Clinical Data Research Network..
21.
2014
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PaTH: towards a learning health system in the Mid-Atlantic region..
21.
2014
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An electronic health record driven algorithm to identify incident antidepressant medication users..
21.
2014
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Paving the COWpath: data-driven design of pediatric order sets..
21.
2014
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Normalization and standardization of electronic health records for high-throughput phenotyping: the SHARPn consortium..
20.
2013
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Sociotechnical challenges to developing technologies for patient access to health information exchange data..
21.
2013
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Implementing health information exchange for public health reporting: a comparison of decision and risk management of three regional health information organizations in New York state..
21.
2013
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Use of computerized algorithm to identify individuals in need of testing for celiac disease..
20.
2013
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A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury..
20.
2013
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A long-term follow-up evaluation of electronic health record prescribing safety..
20.
2013
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When does adoption of health information technology by physician practices lead to use by physicians within the practice?.
20.
2013
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A system dynamics evaluation model: implementation of health information exchange for public health reporting..
20.
2013
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A semantic-web oriented representation of the clinical element model for secondary use of electronic health records data..
20.
2012
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Changes to the electronic health records market in light of health information technology certification and meaningful use..
20.
2012
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Consumer experience with and attitudes toward health information technology: a nationwide survey..
20.
2012
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Factors influencing use of an e-health website in a community sample of older adults..
20.
2012
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AMIA Board white paper: definition of biomedical informatics and specification of core competencies for graduate education in the discipline..
19.
2012
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Importance of multi-modal approaches to effectively identify cataract cases from electronic health records..
19.
2012
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Ambulatory prescribing errors among community-based providers in two states..
19.
2011
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Detecting pregnancy use of non-hormonal category X medications in electronic medical records..
18 Suppl 1.
2011
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President's column: subspecialty certification in clinical informatics..
18.
2011
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Transitioning between ambulatory EHRs: a study of practitioners' perspectives..
19.
2011
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The Triangle Model for evaluating the effect of health information technology on healthcare quality and safety..
19.
2011
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A global travelers' electronic health record template standard for personal health records..
19.
2011
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Evaluating health information technology in community-based settings: lessons learned..
18.
2011
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AMIA president's column: AMIA and HIT policy activities..
18.
2011
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Mapping clinical phenotype data elements to standardized metadata repositories and controlled terminologies: the eMERGE Network experience..
18.
2011
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Characteristics and effects of nurse dosing over-rides on computer-based intensive insulin therapy protocol performance..
18.
2011
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Use of electronic clinical documentation: time spent and team interactions..
18.
2011
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Factors motivating and affecting health information exchange usage..
18.
2011
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AMIA president's message..
18.
2011
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Anticipating and addressing the unintended consequences of health IT and policy: a report from the AMIA 2009 Health Policy Meeting..
18.
2011
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Leveraging informatics for genetic studies: use of the electronic medical record to enable a genome-wide association study of peripheral arterial disease..
17.
2010
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Analyzing categorical information in two publicly available drug terminologies: RxNorm and NDF-RT..
17.
2010
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Health information exchange: persistent challenges and new strategies..
17.
2010
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Quantifying clinical narrative redundancy in an electronic health record..
17.
2010
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Don E. Detmer and the American Medical Informatics Association: an appreciation..
16.
2009
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Presentation of the 2008 Morris F. Collen Award to Robert A. Greenes..
16.
2009
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Physicians' use of key functions in electronic health records from 2005 to 2007: a statewide survey..
16.
2009
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LexGrid: a framework for representing, storing, and querying biomedical terminologies from simple to sublime..
16.
2009
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Topological analysis of large-scale biomedical terminology structures..
14.
2007
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Discovering how to think about a hospital patient information system by struggling to evaluate it: a committee's journal..
14.
2007
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Evaluation of an online platform for cancer patient self-reporting of chemotherapy toxicities..
14.
2007
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Correlates of electronic health record adoption in office practices: a statewide survey..
14.
2006
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Human and automated coding of rehabilitation discharge summaries according to the International Classification of Functioning, Disability, and Health..
13.
2006
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Return on investment for a computerized physician order entry system..
13.
2006
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Training the next generation of informaticians: the impact of "BISTI" and bioinformatics--a report from the American College of Medical Informatics..
11.
2004
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The InterMed approach to sharable computer-interpretable guidelines: a review..
11.
2003
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Comparing computer-interpretable guideline models: a case-study approach..
10.
2003
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Design and applications of a multimodality image data warehouse framework..
9.
2002
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Training synergies between medical informatics and health services research: successes and challenges..
9.
2002
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Are medical informatics and nursing informatics distinct disciplines? The 1999 ACMI debate..
7.
2000
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Representing clinical guidelines in GLIF: individual and collaborative expertise..
5.
1998
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The guideline interchange format: a model for representing guidelines..
5.
1998
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A cryptologic based trust center for medical images..
3.
1996
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The federal role in the health information infrastructure: a debate of the pros and cons of government intervention..
3.
1996
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The PEN-Ivory project: exploring user-interface design for the selection of items from large controlled vocabularies of medicine..
3.
1996
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Ten principles for data sharing and commercialization..
28.
2021
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Further revamping VA's NDF-RT drug terminology for clinical research..
18.
2011
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Human Brain Program Research Progress in biomedical imaging/neuroscience, 2001..
8.
2001
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Informatics at NIH..
7.
2000
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Response to letter to the Editor on "Assessing the capacity of social determinants of health data to augment predictive models identifying patients in need of wraparound social services".
2018
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The potential value of social determinants of health in predicting health outcomes.
2018
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Large language models in biomedicine and health: current research landscape and future directions..
31.
2024
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Electronic health records-driven phenotyping: challenges, recent advances, and perspectives..
20.
2013
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AMIA president's message..
18.
2011
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Human brain program research progress in bioinformatics/ neuroinformatics..
8.
2001
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Dehumanization of patient care--are computers the problem or the solution?.
1.
1994
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The application of artificial intelligence and data integration in COVID-19 studies: a scoping review.
2021
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Measurement of clinical documentation burden among physicians and nurses using electronic health records: a scoping review.
2021
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Mapping scientific landscapes in UMLS research: a scientometric review.
2020
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Effects of health information technology on patient outcomes: a systematic review.
2015
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What should we measure? Conceptualizing usage in health information exchange.
2010
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