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Author Details

Robert R Freimuth
Center for Individualized Medicine, Mayo Clinic
2000
86
28
PMIDPaper TitleJournal TitlePublished Year
38037121Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup.J Am Med Inform Assoc2024
36540993Development and application of a computable genotype model in the GA4GH Variation Representation Specification.Pac Symp Biocomput2023
37387049Representing NIH Genetic Test Registry Data in the FHIR Genomic Study Resource.Stud Health Technol Inform2023
37373918Clinician Perspectives on Clinical Decision Support for Familial Hypercholesterolemia.J Pers Med2023
35331649Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.Genet Med2022
35705716The GA4GH Phenopacket schema defines a computable representation of clinical data.Nat Biotechnol2022
36222570Leveraging a pharmacogenomics knowledgebase to formulate a drug response phenotype terminology for genomic medicine.Bioinformatics2022
35090449Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.BMC Med Inform Decis Mak2022
33447854Recommendations for the safe, effective use of adaptive CDS in the US healthcare system: an AMIA position paper.J Am Med Inform Assoc2021
33930535Genomic considerations for FHIR®; eMERGE implementation lessons.J Biomed Inform2021
35072136GA4GH: International policies and standards for data sharing across genomic research and healthcare.Cell Genom2021
35311178The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification.Cell Genom2021
33979874Infobuttons for Genomic Medicine: Requirements and Barriers.Appl Clin Inform2021
31378813Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol).Int J Epidemiol2020
36644330Deploying Clinical Decision Support for Familial Hypercholesterolemia.ACI open2020
31837229Translational Informatics Connects Real-World Information to Knowledge in an Increasingly Data-Driven World.Clin Pharmacol Ther2020
32717811An Implementation Science Framework to Develop a Clinical Decision Support Tool for Familial Hypercholesterolemia.J Pers Med2020
32669677Participant choices for return of genomic results in the eMERGE Network.Genet Med2020
32246132A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.Nat Genet2020
32377377Challenges in returning results in a genomic medicine implementation study: the Return of Actionable Variants Empirical (RAVE) study.NPJ Genom Med2020
32323283Sync for Genes: Making Clinical Genomics Available for Precision Medicine at the Point-of-Care.Appl Clin Inform2020
31258986A Decade of Translational Bioinformatics: A Retrospective Analysis of "Year-in-Review" Presentations.AMIA Jt Summits Transl Sci Proc2019
31737042Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network.Front Genet2019
30311374ClinGen Allele Registry links information about genetic variants.Hum Mutat2018
29888091Prototype of a Standards-Based EHR and Genetic Test Reporting Tool Coupled with HL7-Compliant Infobuttons.AMIA Jt Summits Transl Sci Proc2018
29860405Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.J Am Med Inform Assoc2018
30392543The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results.Mayo Clin Proc2018
30311379ClinGen advancing genomic data-sharing standards as a GA4GH driver project.Hum Mutat2018
27441996Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC).Genet Med2017
28109071Implementing Genomic Clinical Decision Support for Drug-Based Precision Medicine.CPT Pharmacometrics Syst Pharmacol2017
28269911Knowledge as a Service at the Point of Care.AMIA Annu Symp Proc2017
28502727Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.J Mol Diagn2017
28090649The Pharmacogenomics Research Network Translational Pharmacogenetics Program: Outcomes and Metrics of Pharmacogenetic Implementations Across Diverse Healthcare Systems.Clin Pharmacol Ther2017
27026620Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).J Am Med Inform Assoc2016
26479518Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting.Clin Pharmacol Ther2016
27652374Practical considerations for implementing genomic information resources. Experiences from eMERGE and CSER.Appl Clin Inform2016
27579472Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard.Appl Clin Inform2016
26778834The genomic CDS sandbox: An assessment among domain experts.J Biomed Inform2016
26911808Harnessing next-generation informatics for personalizing medicine: a report from AMIA's 2014 Health Policy Invitational Meeting.J Am Med Inform Assoc2016
27107452An informatics research agenda to support precision medicine: seven key areas.J Am Med Inform Assoc2016
25880555Pharmacogenomic knowledge representation, reasoning and genome-based clinical decision support based on OWL 2 DL ontologies.BMC Med Inform Decis Mak2015
26430534A conceptual model for translating omic data into clinical action.J Pathol Inform2015
26419264Analyzing the potential for incorrect haplotype calls with different pharmacogenomic assays in different populations: a simulation based on 1000 Genomes data.Pharmacogenomics2015
26958298Creating Shareable Clinical Decision Support Rules for a Pharmacogenomics Clinical Guideline Using Structured Knowledge Representation.AMIA Annu Symp Proc2015
26142422CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.J Am Med Inform Assoc2015
23978487Development and use of active clinical decision support for preemptive pharmacogenomics.J Am Med Inform Assoc2014
25954573Simplifying complex clinical element models to encourage adoption.AMIA Jt Summits Transl Sci Proc2014
25954402A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project.AMIA Annu Symp Proc2014
25954360Evaluation of RxNorm for Medication Clinical Decision Support.AMIA Annu Symp Proc2014
24561393Clinical Pharmacogenetics Implementation Consortium Guidelines for HLA-B Genotype and Abacavir Dosing: 2014 update.Clin Pharmacol Ther2014
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Collaborators

Brown University, Brown University Warren Alpert Medical School, Dartmouth-Hitchcock Medical Center, Harvard School of Public Health, Johns Hopkins Medicine, Mayo Clinic Minnesota
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Mayo Clinic
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University of Washington Medical Center
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Co-authored papers 12
Cornell University
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Northwestern University Feinberg School of Medicine
Co-authored papers 11
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Co-authored papers 10
Vanderbilt University Medical Center
Co-authored papers 9
University of Maryland Baltimore County
Co-authored papers 9
Center for Precision Medicine and Functional Genomics, Utah Tech University
Co-authored papers 8
St. Jude Children's Research Hospital Memphis
Co-authored papers 8
Stanford University
Co-authored papers 7
Broad Institute of MIT and Harvard
Co-authored papers 7
Institute for Clinical & Translational Research.
Co-authored papers 7
Departments of Pharmaceutical Sciences.
Co-authored papers 6
Stanford University
Co-authored papers 6
The Broad Institute of MIT and Harvard
Co-authored papers 6
Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis
Co-authored papers 6
Biomedical Ethics, Mayo Clinic and Foundation
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Baylor College of Medicine
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Center for Applied Genomics, Children's Hospital of Philadelphia
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Institute for Public Health Genetics, University of Washington
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Vanderbilt University
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Institute of Artificial Intelligence, Medical University of Vienna
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Mayo Clinic
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Genomic Medicine Institute
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Northwestern University Feinberg School of Medicine
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