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Author Details

Josh F Peterson
Vanderbilt University Medical Center
2001
133
46
PMIDPaper TitleJournal TitlePublished Year
36005898Scanning the medical phenome to identify new diagnoses after recovery from COVID-19 in a US cohort.J Am Med Inform Assoc2023
37523693Web Exclusive. Annals On Call - When Might Genomic Screening Be Cost-Effective?Ann Intern Med2023
37503263Leveraging Large Language Models for Generating Responses to Patient Messages.medRxiv2023
37503019Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.Res Sq2023
37607538The phenotype-genotype reference map: Improving biobank data science through replication.Am J Hum Genet2023
37461512Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.medRxiv2023
37155986Population Genomic Screening for Three Common Hereditary Conditions : A Cost-Effectiveness Analysis.Ann Intern Med2023
37343562Studying the impact of translational genomic research: Lessons from eMERGE.Am J Hum Genet2023
37337966Phenotypic presentation of Mendelian disease across the diagnostic trajectory in electronic health records.Genet Med2023
37071725Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.Circ Genom Precis Med2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36737471Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.Sci Rep2023
36706849Evaluating and mitigating bias in machine learning models for cardiovascular disease prediction.J Biomed Inform2023
35308936Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation.AMIA Annu Symp Proc2022
35579648Penetrance of Deleterious Clinical Variants.JAMA2022
35862023Impact of a Population Genomic Screening Program on Health Behaviors Related to Familial Hypercholesterolemia Risk Reduction.Circ Genom Precis Med2022
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
35961838Cost-effectiveness of population-wide genomic screening for familial hypercholesterolemia in the United States.J Clin Lipidol2022
33611730CYP2C19 Loss-of-Function Associated with First-Time Ischemic Stroke in Non-surgical Asymptomatic Carotid Artery Stenosis During Clopidogrel Therapy.Transl Stroke Res2022
35227606Cost-effectiveness of population-wide genomic screening for Lynch syndrome in the United States.Genet Med2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
33048353A Tutorial for Pharmacogenomics Implementation Through End-to-End Clinical Decision Support Based on Ten Years of Experience from PREDICT.Clin Pharmacol Ther2021
33564788DrugWAS: Leveraging drug-wide association studies to facilitate drug repurposing for COVID-19.medRxiv2021
33838341Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohort.J Biomed Inform2021
33690885The Case for Expanding the FDA Box Warning on Clopidogrel to CYP2C19 Intermediate Metabolizers.Clin Pharmacol Ther2021
33774203ConceptWAS: A high-throughput method for early identification of COVID-19 presenting symptoms and characteristics from clinical notes.J Biomed Inform2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
34834403Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program.J Pers Med2021
34217153Machine Learning Challenges in Pharmacogenomic Research.Clin Pharmacol Ther2021
34038146The Role of Electronic Health Records in Advancing Genomic Medicine.Annu Rev Genomics Hum Genet2021
33979874Infobuttons for Genomic Medicine: Requirements and Barriers.Appl Clin Inform2021
34314511DrugWAS: Drug-wide Association Studies for COVID-19 Drug Repurposing.Clin Pharmacol Ther2021
34357114Strategies to Integrate Genomic Medicine into Clinical Care: Evidence from the IGNITE Network.J Pers Med2021
33428770Opportunity for Genotype-Guided Prescribing Among Adult Patients in 11 US Health Systems.Clin Pharmacol Ther2021
33309899A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19.J Biomed Inform2021
33246208CYP2C19 Loss-of-Function is Associated with Increased Risk of Ischemic Stroke after Transient Ischemic Attack in Intracranial Atherosclerotic Disease.J Stroke Cerebrovasc Dis2021
32342791The Implementation Chasm Hindering Genome-informed Health Care.J Law Med Ethics2020
32042096Cost-effectiveness of CYP2C19-guided antiplatelet therapy in patients with acute coronary syndrome and percutaneous coronary intervention informed by real-world data.Pharmacogenomics J2020
33200151ConceptWAS: a high-throughput method for early identification of COVID-19 presenting symptoms.medRxiv2020
33315113Prescribing Prevalence of Medications With Potential Genotype-Guided Dosing in Pediatric Patients.JAMA Netw Open2020
33119106Cost-effectiveness of Population-Wide Genomic Screening for Hereditary Breast and Ovarian Cancer in the United States.JAMA Netw Open2020
32747766Correction: Evaluating the extent of reusability of CYP2C19 genotype data among patients genotyped for antiplatelet therapy selection.Genet Med2020
32715662Genetic testing and employer-sponsored wellness programs: An overview of current vendors, products, and practices.Mol Genet Genomic Med2020
32678355Evaluating the extent of reusability of CYP2C19 genotype data among patients genotyped for antiplatelet therapy selection.Genet Med2020
32308829Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.AMIA Annu Symp Proc2020
32413979Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.J Pers Med2020
32134729Health Economics Tools and Precision Medicine: Opportunities and Challenges.Forum Health Econ Policy2020
32349224Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.J Pers Med2020
30298529The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.Genet Epidemiol2019
31453360A Decision-Theoretic Approach to Panel-Based, Preemptive Genotyping.MDM Policy Pract2019
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Collaborators

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Co-authored papers 29
University of Washington Medical Center
Co-authored papers 28
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Co-authored papers 21
University of Missouri School of Medicine, PCORnet Clinical Research Network
Co-authored papers 14
University of Washington Medical Center
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National Institutes of Health
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Co-authored papers 13
American College of Medical Informatics, Department of Veteran Affairs, Harvard University T H Chan School of Public Health, Massachusetts Institute of Technology, The American Society for Clinical Investigation, University of Kentucky, Vanderbilt University Medical Center, Vanderbilt University Medical School
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Mayo Clinic
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Co-authored papers 11
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Co-authored papers 10
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Co-authored papers 10
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Co-authored papers 10
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 10
University of Pennsylvania
Co-authored papers 10
Vanderbilt O'Brien Center for Kidney Disease, Vanderbilt University Medical Center
Co-authored papers 10
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University of Washington
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Center for Individualized Medicine, Mayo Clinic
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Brigham and Women's Hospital Division of General Internal Medicine
Co-authored papers 9
Heersink School of Medicine, University of Alabama at Birmingham
Co-authored papers 9
Vanderbilt University Medical Center
Co-authored papers 9
University of Washington
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Department of Pharmacotherapy and Translational Research, University of Florida
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