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Author Details

Victoria M Pratt
Indiana University School of Medicine
1991
98
33
PMIDPaper TitleJournal TitlePublished Year
37689822The INGENIOUS trial: Impact of pharmacogenetic testing on adverse events in a pragmatic clinical trial.Pharmacogenomics J2023
35134542CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project.J Mol Diagn2022
35342886Pharmacogenomics of Hypertension in CKD: The CKD-PGX Study.Kidney3602022
35660539Design and rationale of GUARDD-US: A pragmatic, randomized trial of genetic testing for APOL1 and pharmacogenomic predictors of antihypertensive efficacy in patients with hypertension.Contemp Clin Trials2022
35452844Analytical Validation of a Computational Method for Pharmacogenetic Genotyping from Clinical Whole Exome Sequencing.J Mol Diagn2022
35931342Characterization of Reference Materials for TPMT and NUDT15: A GeT-RM Collaborative Project.J Mol Diagn2022
35177334Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG).Genet Med2022
35202484PharmVar GeneFocus: CYP3A5.Clin Pharmacol Ther2022
35201852Clinical Opportunities for Germline Pharmacogenetics and Management of Drug-Drug Interactions in Patients With Advanced Solid Cancers.JCO Precis Oncol2022
32702149Tracheal Aspirate as an Alternative Biologic Sample for Pharmacogenomics Testing in Mechanically Ventilated Pediatric Patients.Clin Transl Sci2021
33627827Expanding evidence leads to new pharmacogenomics payer coverage.Genet Med2021
33622053Ending the pharmacogenomic gag rule: the imperative to report all results.Pharmacogenomics2021
34020041Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX: A GeT-RM Collaborative Project.J Mol Diagn2021
34071920Multi-Institutional Implementation of Clinical Decision Support for <i>APOL1, NAT2,</i> and <i>YEATS4</i> Genotyping in Antihypertensive Management.J Pers Med2021
34118403Recommendations for Clinical CYP2D6 Genotyping Allele Selection: A Joint Consensus Recommendation of the Association for Molecular Pathology, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, and the European Society for Pharmacogenomics and Personalized Therapy.J Mol Diagn2021
34282303Multisite investigation of strategies for the clinical implementation of pre-emptive pharmacogenetic testing.Genet Med2021
34109627PharmVar GeneFocus: CYP2C9.Clin Pharmacol Ther2021
33288881Correction: Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.Genet Med2021
33197628Characterization of Reference Materials for Spinal Muscular Atrophy Genetic Testing: A Genetic Testing Reference Materials Coordination Program Collaborative Project.J Mol Diagn2021
32602114PharmVar GeneFocus: CYP2C19.Clin Pharmacol Ther2021
32224869Implementation of a Renal Precision Medicine Program: Clinician Attitudes and Acceptance.Life (Basel)2020
31758698PharmVar and the Landscape of Pharmacogenetic Resources.Clin Pharmacol Ther2020
31888882Influence of Uridine Diphosphate Glucuronosyltransferase Family 1 Member A1 and Solute Carrier Organic Anion Transporter Family 1 Member B1 Polymorphisms and Efavirenz on Bilirubin Disposition in Healthy Volunteers.Drug Metab Dispos2020
33232675BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms.Am J Hum Genet2020
32719393Correction: Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.Genet Med2020
32869452EVEN-PLUS syndrome: A case report with novel variants in HSPA9 and evidence of HSPA9 gene dysfunction.Am J Med Genet A2020
32923881Severe Capecitabine Toxicity Associated With a Rare <i>DPYD</i> Variant Identified Through Whole-Genome Sequencing.JCO Precis Oncol2020
32980074Identifying End Users' Preferences about Structuring Pharmacogenetic Test Orders in an Electronic Health Record System.J Mol Diagn2020
32380173Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists.J Mol Diagn2020
30635623Response to Gammal et al.Genet Med2019
30158693Correction: Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.Genet Med2019
29997387Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.Genet Med2019
29858578Pharmacogenetic testing in the Veterans Health Administration (VHA): policy recommendations from the VHA Clinical Pharmacogenetics Subcommittee.Genet Med2019
31401124Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles: A GeT-RM Collaborative Project.J Mol Diagn2019
31512387An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3.Am J Med Genet A2019
30794985Analytical Validation of Variants to Aid in Genotype-Guided Therapy for Oncology.J Mol Diagn2019
30784356Drug-gene and drug-drug interactions associated with tramadol and codeine therapy in the INGENIOUS trial.Pharmacogenomics2019
31075510Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American Pathologists.J Mol Diagn2019
30489456Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy.Pharmacogenet Genomics2019
29102571Multisite Investigation of Outcomes With Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention.JACC Cardiovasc Interv2018
29914287Standardization can accelerate the adoption of pharmacogenomics: current status and the path forward.Pharmacogenomics2018
30351207Report of Confirmation of the rs7853758 and rs885004 Haplotype in SLC28A3.Genet Test Mol Biomarkers2018
29474986Recommendations for Clinical CYP2C19 Genotyping Allele Selection: A Report of the Association for Molecular Pathology.J Mol Diagn2018
29483503Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes.Nat Commun2018
29280137Multisite Investigation of Strategies for the Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy.Clin Pharmacol Ther2018
28532511Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.BMC Med Genomics2017
28294551The IGNITE Pharmacogenetics Working Group: An Opportunity for Building Evidence with Pharmacogenetic Implementation in a Real-World Setting.Clin Transl Sci2017
28212969Lessons Learned When Introducing Pharmacogenomic Panel Testing into Clinical Practice.Value Health2017
26850569Implementation of a pharmacogenomics consult service to support the INGENIOUS trial.Clin Pharmacol Ther2016
26621101Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project.J Mol Diagn2016
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Collaborators

Stanford University
Co-authored papers 14
Indiana University School of Medicine
Co-authored papers 11
Co-authored papers 9
Stanford University
Co-authored papers 9
Department of Pharmacotherapy and Translational Research, University of Florida
Co-authored papers 9
Stanford University
Co-authored papers 8
Duke University School of Medicine
Co-authored papers 7
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
Northwestern University Feinberg School of Medicine
Co-authored papers 6
University of North Carolina at Chapel Hill
Co-authored papers 6
H. Lee Moffitt Cancer Center and Research Institute
Co-authored papers 5
Department of Pharmacotherapy and Translational Research, University of Florida
Co-authored papers 5
University of Maryland School of Medicine
Co-authored papers 4
University of South Dakota Sanford School of Medicine
Co-authored papers 4
College of Medicine, University of Florida
Co-authored papers 4
David Geffen School of Medicine, university of california los angeles
Co-authored papers 4
University of Victoria
Co-authored papers 4
National Cancer Institute, National Institutes of Health
Co-authored papers 4
Department of Pharmacotherapy & Translational Research, University of Florida
Co-authored papers 4
National Institutes of Health
Co-authored papers 4
Medical College of Wisconsin
Co-authored papers 4
Centers for Disease Control and Prevention
Co-authored papers 3
Oregon Health & Science University (OHSU)
Co-authored papers 3
Co-authored papers 3
Heersink School of Medicine, University of Alabama at Birmingham
Co-authored papers 3
Icahn School of Medicine at Mount Sinai
Co-authored papers 3
Institute for Health Equity Research, Icahn School of Medicine at Mount Sinai
Co-authored papers 3
Durham VA Healthcare System and Duke University
Co-authored papers 3
University of Pennsylvania Perelman School of Medicine
Co-authored papers 3
Vanderbilt University Medical Center
Co-authored papers 3