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Author Details

Patricia A Deverka
Deverka Consulting LLC
1991
63
27
PMIDPaper TitleJournal TitlePublished Year
36854952A review of economic issues for gene-targeted therapies: Value, affordability, and access.Am J Med Genet C Semin Med Genet2023
38065071Genomic medicine year in review: 2023.Am J Hum Genet2023
37435610Payer reimbursement practices and incentives for improving interpretation of germline genetic testing.J Law Biosci2023
35254936Multicancer Screening Tests: Anticipating And Addressing Considerations For Payer Coverage And Patient Access.Health Aff (Millwood)2022
35485600A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.J Am Med Inform Assoc2022
36459977Genomic Medicine Year in Review: 2022.Am J Hum Genet2022
34222015Association of Breast Cancer Screening Behaviors With Stage at Breast Cancer Diagnosis and Potential for Additive Multi-Cancer Detection <i>via</i> Liquid Biopsy Screening: A Claims-Based Study.Front Oncol2021
34861172Genomic medicine year in review: 2021.Am J Hum Genet2021
32389218Use of Real-World Evidence in US Payer Coverage Decision-Making for Next-Generation Sequencing-Based Tests: Challenges, Opportunities, and Potential Solutions.Value Health2020
33275910Genomic Medicine Year in Review: 2020.Am J Hum Genet2020
32715662Genetic testing and employer-sponsored wellness programs: An overview of current vendors, products, and practices.Mol Genet Genomic Med2020
30994069Characterizing the Biomedical Data-Sharing Landscape.J Law Med Ethics2019
32027834Genomic Medicine Year in Review: 2019.Am J Hum Genet2019
31395439Opportunities, resources, and techniques for implementing genomics in clinical care.Lancet2019
30994075The Role of Participants in a Medical Information Commons.J Law Med Ethics2019
30994071Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons.J Law Med Ethics2019
29733704Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?Health Aff (Millwood)2018
30224106Methodological Issues in Assessing the Economic Value of Next-Generation Sequencing Tests: Many Challenges and Not Enough Solutions.Value Health2018
29674586Insurance coverage for genomic tests.Science2018
29460415Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects.Clin Pharmacol Ther2018
29684151A New Framework for Patient Engagement in Cancer Clinical Trials Cooperative Group Studies.J Natl Cancer Inst2018
27657682Payer decision making for next-generation sequencing-based genetic tests: insights from cell-free DNA prenatal screening.Genet Med2017
28406488Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research.Genet Med2017
28188191Payer Coverage for Hereditary Cancer Panels: Barriers, Opportunities, and Implications for the Precision Medicine Initiative.J Natl Compr Canc Netw2017
28212967Decision Making on Medical Innovations in a Changing Health Care Environment: Insights from Accountable Care Organizations and Payers on Personalized Medicine and Other Technologies.Value Health2017
28938910Creating a data resource: what will it take to build a medical information commons?Genome Med2017
29065945EXAMINING EVIDENCE IN U.S. PAYER COVERAGE POLICIES FOR MULTI-GENE PANELS AND SEQUENCING TESTS.Int J Technol Assess Health Care2017
28700544Payer coverage policies for multigene tests.Nat Biotechnol2017
27668172Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel.Appl Transl Genom2016
26633547Generating and evaluating evidence of the clinical utility of molecular diagnostic tests in oncology.Genet Med2016
25274556Comparative effectiveness research and demonstrating clinical utility for molecular diagnostic tests.Clin Chem2015
24634466Evidence of clinical utility: an unmet need in molecular diagnostics for patients with cancer.Clin Cancer Res2014
25298289Clinical integration of next generation sequencing: coverage and reimbursement challenges.J Law Med Ethics2014
25387182Overcoming the reimbursement barriers for clinical sequencing.JAMA2014
25399713Useless until proven effective: the clinical utility of preemptive pharmacogenetic testing.Clin Pharmacol Ther2014
23037935Getting our priorities straight: a novel framework for stakeholder-informed prioritization of cancer genomics research.Genet Med2013
23635833Value-of-information analysis within a stakeholder-driven research prioritization process in a US setting: an application in cancer genomics.Med Decis Making2013
23000081Integrating comparative effectiveness design elements and endpoints into a phase III, randomized clinical trial (SWOG S1007) evaluating oncotypeDX-guided management for women with breast cancer involving lymph nodes.Contemp Clin Trials2013
22274803Prioritization in comparative effectiveness research: the CANCERGEN Experience.Med Care2012
24236417Stakeholder engagement in comparative effectiveness research: how will we measure success?J Comp Eff Res2012
23459832Facilitating comparative effectiveness research in cancer genomics: evaluating stakeholder perceptions of the engagement process.J Comp Eff Res2012
22707880Stakeholder participation in comparative effectiveness research: defining a framework for effective engagement.J Comp Eff Res2012
22481130Stakeholder assessment of the evidence for cancer genomic tests: insights from three case studies.Genet Med2012
19407441Factors influencing uptake of pharmacogenetic testing in a diverse patient population.Public Health Genomics2010
20055709Economic opportunities and challenges for pharmacogenomics.Annu Rev Pharmacol Toxicol2010
20017668Institutional profile. UNC Institute for Pharmacogenomics and Individualized Therapy: interdisciplinary research for individual care.Pharmacogenomics2010
19204417Pharmacogenomics, evidence, and the role of payers.Public Health Genomics2009
18679180Harnessing economic drivers for successful clinical implementation of pharmacogenetic testing.Clin Pharmacol Ther2008
17351847Patient receipt and understanding of written information provided with isotretinoin and estrogen prescriptions.J Gen Intern Med2007
18694212Determining user preferences between touch and pen data entry methods in the Tablet PC computing environment.AMIA Annu Symp Proc2007
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Collaborators

University of Washington Medical Center
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National Institutes of Health
Co-authored papers 8
National Human Genome Research Institute
Co-authored papers 8
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 8
Vanderbilt University Medical Center
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Departments of Pharmaceutical Sciences.
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National Human Genome Research Institute, National Institutes of Health
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and Blood Institute
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Center for Precision Medicine and Functional Genomics, Utah Tech University
Co-authored papers 7
The Jackson Laboratory Cancer Center
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Epstein Health LLC
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Center for Evaluation of Value and Risk in Health, Tufts Medical Center
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University of Washington
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University of Washington Medical Center
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Baylor College of Medicine.
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Arizona State University.
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University of California-San Francisco.
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Patient-Centered Outcomes Research Institute
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Duke University School of Medicine
Co-authored papers 3
Mayo Clinic
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National Human Genome Research Institute
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Centers for Disease Control and Prevention Atlanta GA USA.
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Section of Health Services Evaluation, Mayo Clinic
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Berman Institute of Bioethics, Johns Hopkins University
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College of Public Health, University of South Florida
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Duke University Research Institute
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Georgetown University.
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