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Precision Medicine: From Science To Value

Health Affairs, 2018-05, Vol.37 (5), p.694-701

2018

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Availability and funding of clinical genomic sequencing globally

BMJ global health, 2021-02, Vol.6 (2), p.e004415

2021

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Assessing the Value and Implications of Personalized/Precision Medicine and the “Lessons Learned” for Emerging Technologies: An Introduction

Value in health, 2017, Vol.20 (1), p.30-31

Phillips, Kathryn A., PhD

2017

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Evolving Payer Coverage Policies on Genomic Sequencing Tests: Beginning of the End or End of the Beginning?

JAMA : the journal of the American Medical Association, 2018-06, Vol.319 (23), p.2379

Phillips, Kathryn A.

2018

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Potential savings from substituting generic drugs for brand-name drugs: medical expenditure panel survey, 1997-2000

Annals of internal medicine, 2005-06, Vol.142 (11), p.891

2005

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Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?

Health Affairs, 2018-05, Vol.37 (5), p.710-716

2018

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Methods for Moving the Evaluation of Precision Medicine Into Practice and Policy

Value in health, 2020-05, Vol.23 (5), p.527-528

Phillips, Kathryn A.

2020

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“What Goes Around Comes Around”: Lessons Learned from Economic Evaluations of Personalized Medicine Applied to Digital Medicine

Value in health, 2017, Vol.20 (1), p.47-53

2017

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Measuring Patient Preferences for Colorectal Cancer Screening Using a Choice-Format Survey

Value in health, 2007-09, Vol.10 (5), p.415-430

2007

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Decision Making on Medical Innovations in a Changing Health Care Environment: Insights from Accountable Care Organizations and Payers on Personalized Medicine and Other Technologies

Value in health, 2017, Vol.20 (1), p.40-46

2017

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Assessing the Value of Next-Generation Sequencing Technologies: An Introduction

Value in health, 2018-09, Vol.21 (9), p.1031-1032

Phillips, Kathryn A.

2018

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User characteristics and out-of-pocket expenditures for progestin-only versus combined oral contraceptives

Contraception (Stoneham), 2012-12, Vol.86 (6), p.666-672

2012

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Eligibility criteria in private and public coverage policies for BRCA genetic testing and genetic counseling

Genetics in medicine, 2011-12, Vol.13 (12), p.1045-1050

2011

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CMS Coverage With Evidence Development-Challenges and Opportunities for Improvement

JAMA health forum, 2022-09, Vol.3 (9), p.e223061-e223061

Phillips, Kathryn A

2022

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Clinical practice patterns and cost effectiveness of human epidermal growth receptor 2 testing strategies in breast cancer patients

Cancer, 2009-11, Vol.115 (22), p.5166-5174

2009

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Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis

Annals of internal medicine, 2011-07, Vol.155 (2), p.69

2011

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Expanding Use of Clinical Genome Sequencing and the Need for More Data on Implementation

JAMA : the journal of the American Medical Association, 2020-11, Vol.324 (20), p.2029

2020

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Multicancer Screening Tests: Anticipating And Addressing Considerations For Payer Coverage And Patient Access

Health affairs (Millwood, Va.), 2022-03, Vol.41 (3), p.383-2

2022

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Use of Real-World Evidence in US Payer Coverage Decision-Making for Next-Generation Sequencing–Based Tests: Challenges, Opportunities, and Potential Solutions

Value in health, 2020-05, Vol.23 (5), p.540-550

2020

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Emergence of Hybrid Models of Genetic Testing Beyond Direct-to-Consumer or Traditional Labs

JAMA : the journal of the American Medical Association, 2019-06, Vol.321 (24), p.2403

2019

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Personalized medicine and oncology practice guidelines: a case study of contemporary biomarkers in colorectal cancer

Journal of the National Comprehensive Cancer Network, 2011-01, Vol.9 (1), p.13-25

2011

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Assessments of the Value of New Interventions Should Include Health Equity Impact

PharmacoEconomics, 2022-05, Vol.40 (5), p.489-495

2022

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Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS)

Genetics in medicine, 2020-02, Vol.22 (2), p.283-291

2020

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Most Americans Do Not Believe That There Is An Association Between Health Care Prices And Quality Of Care

Health Affairs, 2016-04, Vol.35 (4), p.647-653

2016

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Private Payer and Medicare Coverage for Circulating Tumor DNA Testing: A Historical Analysis of Coverage Policies From 2015 to 2019

Journal of the National Comprehensive Cancer Network, 2020-07, Vol.18 (7), p.866-872

2020

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Precision Medicine: From Science To Value

Availability and funding of clinical genomic sequencing globally

Assessing the Value and Implications of Personalized/Precision Medicine and the “Lessons Learned” for Emerging Technologies: An Introduction

Evolving Payer Coverage Policies on Genomic Sequencing Tests: Beginning of the End or End of the Beginning?

Potential savings from substituting generic drugs for brand-name drugs: medical expenditure panel survey, 1997-2000

Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?

Methods for Moving the Evaluation of Precision Medicine Into Practice and Policy

“What Goes Around Comes Around”: Lessons Learned from Economic Evaluations of Personalized Medicine Applied to Digital Medicine

Measuring Patient Preferences for Colorectal Cancer Screening Using a Choice-Format Survey

Decision Making on Medical Innovations in a Changing Health Care Environment: Insights from Accountable Care Organizations and Payers on Personalized Medicine and Other Technologies

Assessing the Value of Next-Generation Sequencing Technologies: An Introduction

User characteristics and out-of-pocket expenditures for progestin-only versus combined oral contraceptives

Eligibility criteria in private and public coverage policies for BRCA genetic testing and genetic counseling

CMS Coverage With Evidence Development-Challenges and Opportunities for Improvement

Clinical practice patterns and cost effectiveness of human epidermal growth receptor 2 testing strategies in breast cancer patients

Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis

Expanding Use of Clinical Genome Sequencing and the Need for More Data on Implementation

Multicancer Screening Tests: Anticipating And Addressing Considerations For Payer Coverage And Patient Access

Use of Real-World Evidence in US Payer Coverage Decision-Making for Next-Generation Sequencing–Based Tests: Challenges, Opportunities, and Potential Solutions

Emergence of Hybrid Models of Genetic Testing Beyond Direct-to-Consumer or Traditional Labs

Personalized medicine and oncology practice guidelines: a case study of contemporary biomarkers in colorectal cancer

Assessments of the Value of New Interventions Should Include Health Equity Impact

Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS)

Most Americans Do Not Believe That There Is An Association Between Health Care Prices And Quality Of Care

Private Payer and Medicare Coverage for Circulating Tumor DNA Testing: A Historical Analysis of Coverage Policies From 2015 to 2019

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