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Author Details

Shirley V Wang
Brigham and Women's Hospital, Harvard Medical School
2009
90
25
PMIDPaper TitleJournal TitlePublished Year
37853843High-Dose vs. Standard-Dose Influenza Vaccine and Cardiopulmonary Hospitalization or Mortality: Emulating the INVESTED Trial Using Insurance Claims Data.Clin Pharmacol Ther2024
36215113HARmonized Protocol Template to Enhance Reproducibility of hypothesis evaluating real-world evidence studies on treatment effects: A good practices report of a joint ISPE/ISPOR task force.Pharmacoepidemiol Drug Saf2023
37597260Comparison of EHR Data-Completeness in Patients with Different Types of Medical Insurance Coverage in the United States.Clin Pharmacol Ther2023
37549393Comparative Effectiveness and Safety of Generic Versus Brand-Name Fluticasone-Salmeterol to Treat Chronic Obstructive Pulmonary Disease.Ann Intern Med2023
37502999DESIGN DIFFERENCES EXPLAIN VARIATION IN RESULTS BETWEEN RANDOMIZED TRIALS AND THEIR NON-RANDOMIZED EMULATIONS.medRxiv2023
37606676Understanding the Facets of Emulating Randomized Clinical Trials-Reply.JAMA2023
37340238Use of Electronic Health Record Data for Drug Safety Signal Identification: A Scoping Review.Drug Saf2023
37365904Predicting Treatment Effects of a New-to-Market Drug in Clinical Practice Based on Phase III Randomized Trial Results.Clin Pharmacol Ther2023
37097356Emulation of Randomized Clinical Trials With Nonrandomized Database Analyses: Results of 32 Clinical Trials.JAMA2023
37026443The Impact of Longitudinal Data-Completeness of Electronic Health Record Data on the Prediction Performance of Clinical Risk Scores.Clin Pharmacol Ther2023
36408668The Aetion Coalition to Advance Real-World Evidence through Randomized Controlled Trial Emulation Initiative: Oncology.Clin Pharmacol Ther2023
36464785Prospective validation of a dynamic prognostic model for identifying COVID-19 patients at high risk of rapid deterioration.Pharmacoepidemiol Drug Saf2023
34416020Assessing and Interpreting Real-World Evidence Studies: Introductory Points for New Reviewers.Clin Pharmacol Ther2022
35520277A Framework for Visualizing Study Designs and Data Observability in Electronic Health Record Data.Clin Epidemiol2022
36075314Understanding variation in the results of real-world evidence studies that seem to address the same question.J Clin Epidemiol2022
35868493Gastrointestinal prophylaxis for COVID-19: an illustration of severe bias arising from inappropriate comparators in observational studies.J Clin Epidemiol2022
36241338HARmonized Protocol Template to Enhance Reproducibility of Hypothesis Evaluating Real-World Evidence Studies on Treatment Effects: A Good Practices Report of a Joint ISPE/ISPOR Task Force.Value Health2022
35984046Visualizations throughout pharmacoepidemiology study planning, implementation, and reporting.Pharmacoepidemiol Drug Saf2022
35947646Real-World Evidence Prediction of a Phase IV Oncology Trial: Comparative Degarelix vs Leuprolide Safety.JNCI Cancer Spectr2022
35092316Transparency of high-dimensional propensity score analyses: Guidance for diagnostics and reporting.Pharmacoepidemiol Drug Saf2022
32777229Screening Medications for Association with Progression to Wet Age-Related Macular Degeneration.Ophthalmology2021
33715267Control yourself: ISPE-endorsed guidance in the application of self-controlled study designs in pharmacoepidemiology.Pharmacoepidemiol Drug Saf2021
33615330A General Propensity Score for Signal Identification Using Tree-Based Scan Statistics.Am J Epidemiol2021
33834577Online tool to create publication ready graphical depictions of longitudinal study design implemented in healthcare databases.Pharmacoepidemiol Drug Saf2021
34931012Broadening the reach of the FDA Sentinel system: A roadmap for integrating electronic health record data in a causal analysis framework.NPJ Digit Med2021
34277962A novel data mining application to detect safety signals for newly approved medications in routine care of patients with diabetes.Endocrinol Diabetes Metab2021
33436424STaRT-RWE: structured template for planning and reporting on the implementation of real world evidence studies.BMJ2021
33423046Active Surveillance of the Safety of Medications Used During Pregnancy.Am J Epidemiol2021
31569120Use of Time-Dependent Propensity Scores to Adjust Hazard Ratio Estimates in Cohort Studies with Differential Depletion of Susceptibles.Epidemiology2020
31922560Comparison of Machine Learning Methods With Traditional Models for Use of Administrative Claims With Electronic Medical Records to Predict Heart Failure Outcomes.JAMA Netw Open2020
32105168Application of a Graphical Depiction of Longitudinal Study Designs to Managed Care Pharmacy Research.J Manag Care Spec Pharm2020
32639512Using the Case-Crossover Design to Assess Short-Term Risks of Bleeding and Arterial Thromboembolism After Switching Between Oral Anticoagulants in a Population-Based Cohort of Patients With Atrial Fibrillation.Am J Epidemiol2020
32606986Risk Factors for Heart Failure with Preserved or Reduced Ejection Fraction Among Medicare Beneficiaries: Application of Competing Risks Analysis and Gradient Boosted Model.Clin Epidemiol2020
32940229Improving Transparency to Build Trust in Real-World Secondary Data Studies for Hypothesis Testing-Why, What, and How: Recommendations and a Road Map from the Real-World Evidence Transparency Initiative.Value Health2020
32924243Improving transparency to build trust in real-world secondary data studies for hypothesis testing-Why, what, and how: recommendations and a road map from the real-world evidence transparency initiative.Pharmacoepidemiol Drug Saf2020
32613596Determining Which of Several Simultaneously Administered Vaccines Increase Risk of an Adverse Event.Drug Saf2020
32250527Transparency in real-world evidence (RWE) studies to build confidence for decision-making: Reporting RWE research in diabetes.Diabetes Obes Metab2020
32113627Comparison of Different Case-Crossover Variants in Handling Exposure-Time Trend or Persistent-User Bias: Using Dipeptidyl Peptidase-4 Inhibitors and the Risk of Heart Failure as an Example.Value Health2020
32548875Bias in case-crossover studies of medications due to persistent use: A simulation study.Pharmacoepidemiol Drug Saf2020
31020732Evaluating the use of bootstrapping in cohort studies conducted with 1:1 propensity score matching-A plasmode simulation study.Pharmacoepidemiol Drug Saf2019
30107034Using Real-World Data to Extrapolate Evidence From Randomized Controlled Trials.Clin Pharmacol Ther2019
31243156Stepped-wedge randomised trial to evaluate population health intervention designed to increase appropriate anticoagulation in patients with atrial fibrillation.BMJ Qual Saf2019
31452075Transparent Reporting on Research Using Unstructured Electronic Health Record Data to Generate 'Real World' Evidence of Comparative Effectiveness and Safety.Drug Saf2019
31038730Using Healthcare Databases to Refine Understanding of Exploratory Associations Between Drugs and Progression of Open-Angle Glaucoma.Clin Pharmacol Ther2019
30856654Graphical Depiction of Longitudinal Study Designs in Health Care Databases.Ann Intern Med2019
31111340Evaluation of Use of Technologies to Facilitate Medical Chart Review.Drug Saf2019
30873670Commentary in response to Carrigan et al: "An Evaluation of the Impact of Missing Deaths on Overall Survival Analyses of Advanced Non-small Cell Lung Cancer Patients Conducted in an Electronic Health Records Database".Pharmacoepidemiol Drug Saf2019
29318683Prospective surveillance pilot of rivaroxaban safety within the US Food and Drug Administration Sentinel System.Pharmacoepidemiol Drug Saf2018
29862551Identifying signals of interest when screening for drug-outcome associations in health care data.Br J Clin Pharmacol2018
30156128Characteristics of early sacubitril/valsartan patients and considerations for studies in electronic health record data.J Comp Eff Res2018
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Collaborators

Division of Pharmacoepidemiology, Brigham & Women's Hospital, Harvard Medical School
Co-authored papers 47
Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital
Co-authored papers 42
Harvard Medical School
Co-authored papers 14
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Co-authored papers 11
Harvard Medical School and Harvard Pilgrim Health Care Institute
Co-authored papers 9
Center for Drug Evaluation and Research
Co-authored papers 8
Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 7
Harvard Pilgrim Health Care Institute and Harvard Medical School
Co-authored papers 6
Harvard Medical School and Harvard Pilgrim Health Care Institute
Co-authored papers 6
Columbia University
Co-authored papers 4
University of Iowa, School of Public Health
Co-authored papers 4
Quality Use of Medicines and Pharmacy Research Centre, University of South Australia
Co-authored papers 3
University Medical Center Utrecht
Co-authored papers 3
Co-authored papers 3
Columbia University.
Co-authored papers 2
Center for Drug Evaluation and Research
Co-authored papers 2
Center for Drug Evaluation and Research
Co-authored papers 2
Kaiser Permanente Washington Health Research Institute
Co-authored papers 2
Brigham and Women's Hospital.
Co-authored papers 2
Vanderbilt University Medical Center
Co-authored papers 2
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Harvard T.H. Chan School of Public Health
Co-authored papers 1
University of Ottawa
Co-authored papers 1
Harvard Medical School and Harvard Pilgrim Health Care Institute
Co-authored papers 1
University of Utah
Co-authored papers 1
Vanderbilt University Medical Center
Co-authored papers 1
The University of Manchester
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Duke Clinical Research Institute
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Brigham and Women's Hospital Division of General Internal Medicine
Co-authored papers 1
Harvard Medical School
Co-authored papers 1