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Subject Areas on Research
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A Bayesian Approach to Inferring Rates of Selfing and Locus-Specific Mutation.
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A Systematic Framework to Rapidly Obtain Data on Patients with Cancer and COVID-19: CCC19 Governance, Protocol, and Quality Assurance.
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A comparison of NSQIP and CESQIP in data quality and ability to predict thyroidectomy outcomes.
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A hidden Markov model approach to analyze longitudinal ternary outcomes when some observed states are possibly misclassified.
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A longitudinal analysis of data quality in a large pediatric data research network.
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Accuracy of Self-reported Weight in Hispanic/Latino Adults of the Hispanic Community Health Study/Study of Latinos.
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Accuracy of the Liver Imaging Reporting and Data System in Computed Tomography and Magnetic Resonance Image Analysis of Hepatocellular Carcinoma or Overall Malignancy-A Systematic Review.
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Accuracy of the medication list in the electronic health record-implications for care, research, and improvement.
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Analytical Evaluation of the Abbott RealTime CT/NG Assay for Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Rectal and Pharyngeal Swabs.
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Are three-day voiding diaries feasible and reliable? Results from the Symptoms of Lower Urinary Tract Dysfunction Research Network (LURN) cohort.
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Assessing Quality of Surgical Real-World Data from an Automated Electronic Health Record Pipeline.
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Bias from Differential Exposure Measurement Error in a Study of Flight Attendants.
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Biases introduced by filtering electronic health records for patients with "complete data".
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Caveat emptor: the combined effects of multiplicity and selective reporting.
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Claims-based cardiovascular outcome identification for clinical research: Results from 7 large randomized cardiovascular clinical trials.
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Clinical trial metadata: defining and extracting metadata on the design, conduct, results and costs of 125 randomised clinical trials funded by the National Institute for Health Research Health Technology Assessment programme.
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Critical Review of Current Approaches for Echocardiographic Reproducibility and Reliability Assessment in Clinical Research.
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Data quality from a longitudinal study of adolescent health at schools near industrial livestock facilities.
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Dataset for the reporting of carcinoma of the esophagus in resection specimens: recommendations from the International Collaboration on Cancer Reporting.
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Electronic health records to facilitate clinical research.
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Enhancing the value of clinical trials: the role of data sharing.
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Evaluating fitness-for-use of electronic health records in pragmatic clinical trials: reported practices and recommendations.
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Evaluation of Content on Commonly Used Web sites About Induction of Labor and Pain Management During Labor.
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Evaluation of identifier field agreement in linked neonatal records.
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Evaluation of individual and ensemble probabilistic forecasts of COVID-19 mortality in the United States.
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Evaluation of the Use of Cancer Registry Data for Comparative Effectiveness Research.
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Factors Affecting Accuracy of Data Abstracted from Medical Records.
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GRADE guidelines: 21 part 1. Study design, risk of bias, and indirectness in rating the certainty across a body of evidence for test accuracy.
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GRADE guidelines: 21 part 2. Test accuracy: inconsistency, imprecision, publication bias, and other domains for rating the certainty of evidence and presenting it in evidence profiles and summary of findings tables.
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HRS White Paper on interoperability of data from cardiac implantable electronic devices (CIEDs).
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Harms are assessed inconsistently and reported inadequately Part 2: nonsystematic adverse events.
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Harms are assessed inconsistently and reported inadequately part 1: systematic adverse events.
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How to Teach Health IT Evaluation: Recommendations for Health IT Evaluation Courses.
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Important considerations for trials for peripheral arterial disease: Lessons learned from the paclitaxel mortality signal: A report on behalf of the registry assessment for peripheral interventional Devices (RAPID) Paclitaxel Pathways Program.
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Improving Quality and Safety Through Use of Secondary Data: Methods Case Study.
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Laboratory Accuracy Improvement in the UK NEQAS Leucocyte Immunophenotyping Immune Monitoring Program: An Eleven-Year Review via Longitudinal Mixed Effects Modeling.
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Level and Prevalence of Spin in Published Cardiovascular Randomized Clinical Trial Reports With Statistically Nonsignificant Primary Outcomes: A Systematic Review.
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Medical record bias in documentation of obstetric and neonatal clinical quality of care indicators in Uganda.
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Priorities to Overcome Barriers Impacting Data Science Application in Emergency Care Research.
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Real-World Data: Policy Issues Regarding their Access and Use.
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Recommendations for Reporting Machine Learning Analyses in Clinical Research.
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Ten Simple Rules for Effective Statistical Practice.
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The Accuracy of the Patient Health Questionnaire-9 Algorithm for Screening to Detect Major Depression: An Individual Participant Data Meta-Analysis.
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The Clinical Trials Transformation Initiative: Methodology supporting the mission.
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The Complexity of Conducting a Multicenter Clinical Trial: Taking It to the Next Level Stipulated by the Federal Agencies.
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The Impact of a Rigorous Quality Program on 3D Echocardiography Data Quality in an International Multisite Randomized Trial.
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The challenges of data safety monitoring for a pragmatic study: Lessons from the ADAPTABLE study.
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The impact of respiratory gating on improving volume measurement of murine lung tumors in micro-CT imaging.
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The use of real-world data/evidence in regulatory submissions.
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Under-reporting of TB cases and associated factors: a case study in China.
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Using clinical data to effect practice change.
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eSource for Standardized Health Information Exchange in Clinical Research: A Systematic Review.