Information Dissemination
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Subject Areas on Research
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#VascularSurgery.
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A Balanced Data Archiving Policy for Long-Term Studies.
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A Cytometrist's Guide to Coordinating and Performing Effective COVID-19 Research.
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A Shared Vision for Machine Learning in Neuroscience.
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A kernel for the Tropical Disease Initiative.
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A new open-access platform for measuring and sharing mTBI data.
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A proteogenomic survey of the Medicago truncatula genome.
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A randomized controlled trial of health information exchange between human immunodeficiency virus institutions.
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A sea of standards for omics data: sink or swim?
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A theoretical framework for a virtual diabetes self-management community intervention.
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A web-based tool to engage stakeholders in informing research planning for future decisions on emerging materials.
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Accelerating the Evolution of Nonhuman Primate Neuroimaging.
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Access to patient-level data from GlaxoSmithKline clinical trials.
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Affiliate network members as force amplifiers of genomic medicine research.
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Aligning payment reform and delivery innovation in emergency care.
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American Society of Clinical Oncology clinical practice guidelines: opportunities and challenges.
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An Open Resource for Non-human Primate Imaging.
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An i2b2-based, generalizable, open source, self-scaling chronic disease registry.
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An informatics research agenda to support precision medicine: seven key areas.
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Any questions? A concise guide to navigating the Q&A session after a presentation.
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Application description and policy model in collaborative environment for sharing of information on epidemiological and clinical research data sets.
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Assessing the Effectiveness of Evidence-Based Medicine in Practice: A Case Study of First-Time Anterior Shoulder Dislocations.
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Association Between Public Knowledge About COVID-19, Trust in Information Sources, and Adherence to Social Distancing: Cross-Sectional Survey.
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Asthma dissemination around patient-centered treatments in North Carolina (ADAPT-NC): a cluster randomized control trial evaluating dissemination of an evidence-based shared decision-making intervention for asthma management.
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Attitudes of elderly patients and their families toward physician-assisted suicide.
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Audit of Data Sharing by Pharmaceutical Companies for Anticancer Medicines Approved by the US Food and Drug Administration.
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Benefits and Threats to Using Social Media for Presenting and Implementing Evidence.
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Best practices and lessons learned from reuse of 4 patient-derived metabolomics datasets in Alzheimer's disease.
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Beyond MRI: on the scientific value of combining non-human primate neuroimaging with metadata.
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Brief reports for disseminating systematic reviews to nurses.
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Building capacity for advances in tuberculosis research; proceedings of the third RePORT international meeting.
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Building evidence for practice: not without dissemination.
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Bumps and bridges on the road to responsible sharing of clinical trial data.
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COVID-19 interventional trials: Analysis of data sharing intentions during a time of pandemic.
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COVID-19 trials: declarations of data sharing intentions at trial registration and at publication.
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Can You Trust What You Watch? An Assessment of the Quality of Information in Aesthetic Surgery Videos on YouTube.
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Cancer pharmacogenomics and pharmacoepidemiology: setting a research agenda to accelerate translation.
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China's distinctive engagement in global health.
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Citation analysis of the maternal/child nursing literature.
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Collaboration for Alzheimer's Prevention: Principles to guide data and sample sharing in preclinical Alzheimer's disease trials.
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Comprehensive genomic studies: emerging regulatory, strategic, and quality assurance challenges for biorepositories.
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Conducting multisite research studies in nursing education: brief practice of CPR skills as an exemplar.
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Connecting information to improve health.
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Considering the Benefits and Risks of Research Participants' Access to Sequence Data.
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Conversion of cardiovascular conference abstracts to publications.
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Counteracting Health Misinformation: A Role for Medical Journals?
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Creating a transdisciplinary research center to reduce cardiovascular health disparities in Baltimore, Maryland: lessons learned.
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DATA ACCESS. Sharing by design: Data and decentralized commons.
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Data Harmonization for a Molecularly Driven Health System.
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Data Sharing From the Editors' Perspective: Our Hope With Limitations.
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Data Sharing and Embedded Research.
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Data Sharing and Reproducibility of Results-Does It Matter for HIV Nursing?
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Data Sharing at a Crossroads.
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Data Sharing of Imaging in an Evolving Health Care World: Report of the ACR Data Sharing Workgroup, Part 1: Data Ethics of Privacy, Consent, and Anonymization.
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Data Sharing of Imaging in an Evolving Health Care World: Report of the ACR Data Sharing Workgroup, Part 2: Annotation, Curation, and Contracting.
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Data sharing in the undiagnosed diseases network.
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Defining quality, disseminating evidence, and enforcing guidelines for cancer treatment.
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Disseminating trial results: We can have both faster and better.
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Dissemination of CPR video self-instruction materials to secondary trainees: Results from a hospital-based CPR education trial.
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Dissemination of Evidence-based Practice Center reports.
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Dissemination of evidence-based mental health interventions: importance to the trauma field.
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Dissemination of research in clinical nursing journals.
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Dissemination of research into clinical nursing literature.
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Does a controversial topic affect the quality of urologic information on the Internet?
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Does it pay to pay people to share information? Using financial incentives to promote peer referral for mammography among the underinsured.
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Early impact of guideline publication on angiotensin-receptor neprilysin inhibitor use among patients hospitalized for heart failure.
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Effectiveness of an intervention for disseminating Cochrane reviews to nurses.
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Elevator talk: observational study of inappropriate comments in a public space.
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Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
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Enhancing the value of clinical trials: the role of data sharing.
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Ethics challenges in sharing data from pragmatic clinical trials.
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Evaluating common data models for use with a longitudinal community registry.
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Examining the Use of a Social Media Campaign to Increase Engagement for the American Heart Association 2017 Resuscitation Science Symposium.
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Excluding the poor from accessing biomedical literature: a rights violation that impedes global health.
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Exit interview-consultation for research validation and dissemination.
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Extending Our Reach for Greater Impact.
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Face-to-face learning enhances the social transmission of information.
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Federated learning enables big data for rare cancer boundary detection.
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Finding Means to Fulfill the Societal and Academic Imperative for Open Data Access and Sharing.
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First Responder to Genomic Information: A Guide for Primary Care Providers.
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Food and beverage brands that market to children and adolescents on the internet: a content analysis of branded web sites.
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From theory to practice: translating research into health outcomes.
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Graphics for dissemination of meta-analyses to staff nurses.
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Grey literature in meta-analyses.
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Grid Binary LOgistic REgression (GLORE): building shared models without sharing data.
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Grid multi-category response logistic models.
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HIPAA and the Leak of "Deidentified" EHR Data.
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HRS White Paper on interoperability of data from cardiac implantable electronic devices (CIEDs).
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Hat, shade, long sleeves, or sunscreen? Rethinking US sun protection messages based on their relative effectiveness.
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Health data use, stewardship, and governance: ongoing gaps and challenges: a report from AMIA's 2012 Health Policy Meeting.
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Heart Failure Fake News: How Do We Distinguish the Truth?
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How academic physicians can benefit from social media.
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How can evolutionary and biological anthropologists engage broader audiences?
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How do doctors use information in real-time? A qualitative study of internal medicine resident precepting.
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How informatics can potentiate precompetitive open-source collaboration to jump-start drug discovery and development.
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IAEA experience in communicating radiation risks through the RPOP website.
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Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons
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Improving Medication Adherence in Cardiometabolic Disease: Practical and Regulatory Implications.
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Individual Patient Data from the Pivotal Randomized Controlled Trials of Non-Vitamin K Antagonist Oral Anticoagulants in Patients with Atrial Fibrillation (COMBINE AF): Design and Rationale: From the COMBINE AF (A Collaboration between Multiple institutions to Better Investigate Non-vitamin K antagonist oral anticoagulant use in Atrial Fibrillation) Investigators.
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Influence of the Angioplasty Revascularization Investigation National Heart, Lung, and Blood Institute Diabetic Clinical Alert on practice patterns: results from the National Cardiovascular Network Database.
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Infobuttons and classification models: a method for the automatic selection of on-line information resources to fulfill clinicians' information needs.
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Information exchange and decision making in the treatment of Latina and white women with ductal carcinoma in situ.
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Information sources for developing the nursing literature.
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Informed Consent for Electroconvulsive Therapy--Finding Balance.
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Integrating technology into palliative care research.
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Internet food marketing strategies aimed at children and adolescents: a content analysis of food and beverage brand web sites.
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Interpersonal communication as an indirect pathway for the effect of antismoking media content on smoking cessation.
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Introducing the Medical Physics Dataset Article.
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Issues affecting minority participation in research studies of Alzheimer disease.
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Knowledge translation of the American College of Emergency Physicians clinical policy on hypertension.
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LabKey Server NAb: a tool for analyzing, visualizing and sharing results from neutralizing antibody assays.
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Large-scale evaluation of automated clinical note de-identification and its impact on information extraction.
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Learning through the grapevine and the impact of the breadth and depth of social networks.
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Leveraging electronic health records for clinical research.
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Leveraging external data in the design and analysis of clinical trials in neuro-oncology.
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Living laboratory: whole-genome sequencing as a learning healthcare enterprise.
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Looking back and moving forward.
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Managing the risks of therapeutic products: proceedings of a workshop.
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Measuring health care performance now, not tomorrow: essential steps to support effective health reform.
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Medicare data transparency may confuse consumers comparing hospitals for total joint arthroplasty.
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Medicare part D information seeking: the role of recognition of need and patient activation.
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Metabolomics Standards Workshop and the development of international standards for reporting metabolomics experimental results.
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Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases Network.
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Monitoring the world's agriculture.
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NIH MICAD initiative and guest author program opportunities.
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NSF workshop report: discovering general principles of nervous system organization by comparing brain maps across species.
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New Thinking About Thinking, Part 3. Advice on preparing a successful manuscript for Alzheimer's & Dementia.
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Newspaper coverage of maternal health in Bangladesh, Rwanda and South Africa: a quantitative and qualitative content analysis.
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Online Social Media as a Curation Tool for Teaching.
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Open Access Platforms for Sharing Clinical Trial Data--Reply.
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Open Science to Address COVID-19: Sharing Data to Make Our Research Investment Go Further.
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Open access publishing: a disruptive innovation
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Open science: The open clinical trials data journey.
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Opportunities for selective reporting of harms in randomized clinical trials: Selection criteria for non-systematic adverse events.
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PCORnet® 2020: current state, accomplishments, and future directions.
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PEDSnet: a National Pediatric Learning Health System.
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Pan-cancer analysis of whole genomes.
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Partnership-driven Resources to Improve and Enhance Research (PRIMER): a survey of community-engaged researchers and creation of an online toolkit.
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Patient perspectives on the linkage of health data for research: Insights from an online patient community questionnaire.
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Pediatric urology and the internet--does an uncommon topic decrease content quality?
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Peer review: evolution or revolution?
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Practical steps for evidence-based practice: putting one foot in front of the other.
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Pragmatic clinical trials offer unique opportunities for disseminating, implementing, and sustaining evidence-based practices into clinical care: Proceedings of a workshop.
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Precision Medicine: From Science To Value.
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Presenting research to clinicians: strategies for writing about research findings.
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Principal/agent theory and decision making in health care.
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Priorities for autism spectrum disorder risk communication and ethics.
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Promises and pitfalls of data sharing in qualitative research.
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Protecting human security: proposals for the G7 Ise-Shima Summit in Japan.
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Public disclosure of clinical research.
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Public perspectives regarding data-sharing practices in genomics research.
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Publication Rates of Heart Failure Clinical Trials Remain Low.
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Qualitative analysis of Web-based refractive surgery information sessions.
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Radiation effects and risks: overview and a new risk perception index.
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Real-World Data: Policy Issues Regarding their Access and Use.
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Realizing the Full Potential of Precision Medicine in Health and Health Care.
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Recommendations for minimum information for publication of experimental pathology data: MINPEPA guidelines.
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Recommendations from the international stroke genetics consortium, part 2: biological sample collection and storage.
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Recruitment of rural and cognitively impaired older adults for dental research.
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Replicating dissemination and identifying mechanisms of implementation of an empirically supported treatment.
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Reply: Can You Trust What You Watch? An Assessment of the Quality of Information in Aesthetic Surgery Videos on YouTube.
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Reply: Can You Trust What You Watch? An Assessment of the Quality of Information in Aesthetic Surgery Videos on YouTube.
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Reproducible research in medical imaging.
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Research use of electronic health records: patients' perspectives on contact by researchers.
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Response to Watson R (2011) Commentary on Oermann MH, Shaw-Kokot J, Knafl GJ & Dowell J (2010) Dissemination of research into clinical nursing literature. Journal of Clinical Nursing 19, 3435-3442. Journal of Clinical Nursing 20, 595-596.
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Response to letters to the editor concerning AJPA commentary on "data sharing in biological anthropology: Guiding principles and best practices".
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Return of Research Results to Study Participants: Uncharted and Untested.
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Return of individual research results: What do participants prefer and expect?
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SQUIRE Guidelines for reporting improvement studies in healthcare: implications for nursing publications.
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Scalable Collaborative Infrastructure for a Learning Healthcare System (SCILHS): architecture.
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Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.
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Seamless care: what is it; what is its value; what does it require; when might we get it?
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Shared Electronic Health Record Systems: Key Legal and Security Challenges.
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Sharing Antimicrobial Reports for Pediatric Stewardship (SHARPS): A Quality Improvement Collaborative.
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Sharing Data from Cardiovascular Clinical Trials--A Proposal.
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Sharing Data to Accelerate Medicine Development and Improve Neonatal Care: Data Standards and Harmonized Definitions.
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Sharing adverse drug event data using business intelligence technology.
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Sharing confidential data for research purposes: a primer.
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Sharing voxelwise neuroimaging results from rhesus monkeys and other species with Neurovault.
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Sharing your work: building knowledge about nursing care quality.
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Social media in academics and research: 21st-century tools to turbocharge education, collaboration, and dissemination of research findings.
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Social networking and understanding alcohol-associated risk for people with type 1 diabetes: friend or foe?
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Social work competencies in palliative and end-of-life care.
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Start me up: ways to encourage sharing of genomic information with research participants.
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Statistical controversies in clinical research: data access and sharing-can we be more transparent about clinical research? Let's do what's right for patients.
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Stewards of the discipline: The role of referees and peer review
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Symptom prevalence and physiologic biomarkers among adolescents using a mobile phone intervention following hematopoietic stem cell transplantation.
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Ten Simple Rules for Effective Statistical Practice.
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The 2013 US Government Shutdown (#Shutdown) and health: an emerging role for social media.
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The Clinical Trials Transformation Initiative: Methodology supporting the mission.
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The College of American Pathologists Biorepository Accreditation Program: Results from the First 5 Years.
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The ENCODE (ENCyclopedia Of DNA Elements) Project.
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The Firegoose: two-way integration of diverse data from different bioinformatics web resources with desktop applications.
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The Function Biomedical Informatics Research Network Data Repository.
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The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system.
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The Nanomaterial Registry: facilitating the sharing and analysis of data in the diverse nanomaterial community
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The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment.
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The RNA Ontology Consortium: an open invitation to the RNA community.
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The Role and Impact of Social Media in Cardio-oncology During the COVID-19 Pandemic.
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The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.
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The Society of Thoracic Surgeons voluntary public reporting initiative: the first 4 years.
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The US Food and Drug Administration and the Future of Cardiovascular Medicine.
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The attention economy and the EMBS.
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The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism.
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The availability of community ties predicts likelihood of peer referral for mammography: geographic constraints on viral marketing.
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The cancer translational research informatics platform.
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The delivery of public health interventions via the Internet: actualizing their potential.
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The effect of giving global coronary risk information to adults: a systematic review.
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The effectors of innate immunity: DAMPs, DAMEs, or DIMEs?
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The national drug abuse treatment clinical trials network data share project: website design, usage, challenges, and future directions.
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The use of technology for urgent clinician to clinician communications: a systematic review of the literature.
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Time for NIH to lead on data sharing.
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Towards ubiquitous peer review strategies to sustain and enhance a clinical knowledge management framework.
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Transmissibility of the Ice Bucket Challenge among globally influential celebrities: retrospective cohort study.
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Transparency and reproducibility in evolutionary research.
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Transparent sharing of digital health data: A call to action.
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Traveling the Interstices of Data Sharing.
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Turning Data Into Information: Opportunities to Advance Rehabilitation Quality, Research, and Policy.
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Tweeting the meeting: an in-depth analysis of Twitter activity at Kidney Week 2011.
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Updated standardized endpoint definitions for transcatheter aortic valve implantation: the Valve Academic Research Consortium-2 consensus document.
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Updating insights into rosiglitazone and cardiovascular risk through shared data: individual patient and summary level meta-analyses.
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Upgrading a Social Media Strategy to Increase Twitter Engagement During the Spring Annual Meeting of the American Society of Regional Anesthesia and Pain Medicine.
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Use of Open Access Platforms for Clinical Trial Data.
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Use of email in a family practice setting: opportunities and challenges in patient- and physician-initiated communication.
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Use of the Internet for health information by the chronically ill.
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Using Telehealth to Disseminate Primary, Secondary, and Tertiary CVD Interventions to Rural Populations.
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Using social media to create a professional network between physician-trainees and the American Society of Nephrology.
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Video Abstracts: A Fun, Easy Way to Capture Your Audience: Try it!
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Violations of human rights: health practitioners as witnesses.
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Waxholm Space atlas of the Sprague Dawley rat brain.
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WebDISCO: a web service for distributed cox model learning without patient-level data sharing.
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WebGLORE: a web service for Grid LOgistic REgression.
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Websites or Videos: Which Offer Better Information for Patients? A Comparative Analysis of the Quality of YouTube Videos and Websites for Cosmetic Injectables.
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What Medical Informaticians Do With and Think About an International Medical Informatics Listserv: Member Survey Preliminary Findings.
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Who Will Drive the Change? Democratizing Health Data.
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Who owns the genome?
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Why addressing the poor and underinsured is vexing.
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Keywords of People
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Anderson, Ruth A.,
Professor Emerita in the School of Nursing,
School of Nursing
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Johnson, G. Allan,
Charles E. Putman University Distinguished Professor of Radiology,
Biomedical Engineering
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LeBlanc, Thomas William,
Associate Professor of Medicine,
Duke Cancer Institute
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Reiter, Jerome P.,
Professor of Statistical Science,
Nicholas Institute-Energy Initiative
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Sullivan, Daniel Carl,
Professor Emeritus of Radiology,
Radiology
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West, Vivian L,
Clinical Associate in the School of Nursing,
School of Nursing