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Author Details
Full Name
Josh F Peterson
Affiliation
Vanderbilt University Medical Center
ORCID
Career Start Year
2001
Papers
133
H Index
46
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36005898
Scanning the medical phenome to identify new diagnoses after recovery from COVID-19 in a US cohort.
J Am Med Inform Assoc
2023
37523693
Web Exclusive. Annals On Call - When Might Genomic Screening Be Cost-Effective?
Ann Intern Med
2023
37503263
Leveraging Large Language Models for Generating Responses to Patient Messages.
medRxiv
2023
37503019
Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.
Res Sq
2023
37607538
The phenotype-genotype reference map: Improving biobank data science through replication.
Am J Hum Genet
2023
37461512
Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.
medRxiv
2023
37155986
Population Genomic Screening for Three Common Hereditary Conditions : A Cost-Effectiveness Analysis.
Ann Intern Med
2023
37343562
Studying the impact of translational genomic research: Lessons from eMERGE.
Am J Hum Genet
2023
37337966
Phenotypic presentation of Mendelian disease across the diagnostic trajectory in electronic health records.
Genet Med
2023
37071725
Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.
Circ Genom Precis Med
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36737471
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.
Sci Rep
2023
36706849
Evaluating and mitigating bias in machine learning models for cardiovascular disease prediction.
J Biomed Inform
2023
35308936
Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation.
AMIA Annu Symp Proc
2022
35579648
Penetrance of Deleterious Clinical Variants.
JAMA
2022
35862023
Impact of a Population Genomic Screening Program on Health Behaviors Related to Familial Hypercholesterolemia Risk Reduction.
Circ Genom Precis Med
2022
35446370
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.
JAMA Oncol
2022
35961838
Cost-effectiveness of population-wide genomic screening for familial hypercholesterolemia in the United States.
J Clin Lipidol
2022
33611730
CYP2C19 Loss-of-Function Associated with First-Time Ischemic Stroke in Non-surgical Asymptomatic Carotid Artery Stenosis During Clopidogrel Therapy.
Transl Stroke Res
2022
35227606
Cost-effectiveness of population-wide genomic screening for Lynch syndrome in the United States.
Genet Med
2022
35216901
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
Genet Med
2022
33048353
A Tutorial for Pharmacogenomics Implementation Through End-to-End Clinical Decision Support Based on Ten Years of Experience from PREDICT.
Clin Pharmacol Ther
2021
33564788
DrugWAS: Leveraging drug-wide association studies to facilitate drug repurposing for COVID-19.
medRxiv
2021
33838341
Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohort.
J Biomed Inform
2021
33690885
The Case for Expanding the FDA Box Warning on Clopidogrel to CYP2C19 Intermediate Metabolizers.
Clin Pharmacol Ther
2021
33774203
ConceptWAS: A high-throughput method for early identification of COVID-19 presenting symptoms and characteristics from clinical notes.
J Biomed Inform
2021
34377931
Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.
JNCI Cancer Spectr
2021
34834403
Impact of Updating Pharmacogenetic Results: Lessons Learned from the PREDICT Program.
J Pers Med
2021
34217153
Machine Learning Challenges in Pharmacogenomic Research.
Clin Pharmacol Ther
2021
34038146
The Role of Electronic Health Records in Advancing Genomic Medicine.
Annu Rev Genomics Hum Genet
2021
33979874
Infobuttons for Genomic Medicine: Requirements and Barriers.
Appl Clin Inform
2021
34314511
DrugWAS: Drug-wide Association Studies for COVID-19 Drug Repurposing.
Clin Pharmacol Ther
2021
34357114
Strategies to Integrate Genomic Medicine into Clinical Care: Evidence from the IGNITE Network.
J Pers Med
2021
33428770
Opportunity for Genotype-Guided Prescribing Among Adult Patients in 11 US Health Systems.
Clin Pharmacol Ther
2021
33309899
A 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 Inform
2021
33246208
CYP2C19 Loss-of-Function is Associated with Increased Risk of Ischemic Stroke after Transient Ischemic Attack in Intracranial Atherosclerotic Disease.
J Stroke Cerebrovasc Dis
2021
32342791
The Implementation Chasm Hindering Genome-informed Health Care.
J Law Med Ethics
2020
32042096
Cost-effectiveness of CYP2C19-guided antiplatelet therapy in patients with acute coronary syndrome and percutaneous coronary intervention informed by real-world data.
Pharmacogenomics J
2020
33200151
ConceptWAS: a high-throughput method for early identification of COVID-19 presenting symptoms.
medRxiv
2020
33315113
Prescribing Prevalence of Medications With Potential Genotype-Guided Dosing in Pediatric Patients.
JAMA Netw Open
2020
33119106
Cost-effectiveness of Population-Wide Genomic Screening for Hereditary Breast and Ovarian Cancer in the United States.
JAMA Netw Open
2020
32747766
Correction: Evaluating the extent of reusability of CYP2C19 genotype data among patients genotyped for antiplatelet therapy selection.
Genet Med
2020
32715662
Genetic testing and employer-sponsored wellness programs: An overview of current vendors, products, and practices.
Mol Genet Genomic Med
2020
32678355
Evaluating the extent of reusability of CYP2C19 genotype data among patients genotyped for antiplatelet therapy selection.
Genet Med
2020
32308829
Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.
AMIA Annu Symp Proc
2020
32413979
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.
J Pers Med
2020
32134729
Health Economics Tools and Precision Medicine: Opportunities and Challenges.
Forum Health Econ Policy
2020
32349224
Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.
J Pers Med
2020
30298529
The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.
Genet Epidemiol
2019
31453360
A Decision-Theoretic Approach to Panel-Based, Preemptive Genotyping.
MDM Policy Pract
2019
1 - 50 of 133
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row(s) 1 - 30 of 30
Collaborators
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Vanderbilt University
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Vanderbilt University Medical Center
Co-authored papers
29
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Co-authored papers
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Vanderbilt University Medical Center.
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Co-authored papers
14
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University of Washington Medical Center
Co-authored papers
14
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Michael Matheny
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
Co-authored papers
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Mayo Clinic
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Wei-Qi Wei
Vanderbilt University Medical Center
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11
Jill M Pulley
Vanderbilt University School of Medicine
Co-authored papers
10
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers
10
Luke V Rasmussen
Northwestern University Feinberg School of Medicine
Co-authored papers
10
Maureen E Smith
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers
10
Kevin B Johnson
University of Pennsylvania
Co-authored papers
10
Edward D Siew
Vanderbilt O'Brien Center for Kidney Disease, Vanderbilt University Medical Center
Co-authored papers
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Talat Alp Ikizler
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