Clinical integration of next generation sequencing: coverage and reimbursement challenges. (Q30355277)

20 August 2017

Clinical integration of next generation sequencing: coverage and reimbursement challenges. (English)

1 reference

20 August 2017

Patricia A Deverka

1

1 reference

PMCID

5108048

20 August 2017

Jennifer C Dreyfus

series ordinal

2

1 reference

20 August 2017

1 January 2014

1 reference

Journal of Law, Medicine, and Ethics

20 August 2017

1 reference

20 August 2017

42 Suppl 1

1 reference

20 August 2017

22-41

1 reference

Clinical interpretation and implications of whole-genome sequencing

20 August 2017

1 reference

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First FDA authorization for next-generation sequencer

3 June 2018

1 reference

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3 June 2018

1 reference

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3 June 2018

1 reference

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Reporting genomic sequencing results to ordering clinicians: incidental, but not exceptional

3 June 2018

1 reference

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Recommendations for returning genomic incidental findings? We need to talk!

3 June 2018

1 reference

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ACMG clinical laboratory standards for next-generation sequencing

3 June 2018

1 reference

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3 June 2018

1 reference

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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

3 June 2018

1 reference

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Translating next generation sequencing to practice: opportunities and necessary steps

3 June 2018

1 reference

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3 June 2018

1 reference

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3 June 2018

1 reference

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3 June 2018

1 reference

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Translational utility of next-generation sequencing

3 June 2018

1 reference

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3 June 2018

1 reference

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3 June 2018

1 reference

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Next-generation sequencing in the clinic: are we ready?

3 June 2018

1 reference

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Informatics and clinical genome sequencing: opening the black box.

3 June 2018

1 reference

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Improving the efficiency and relevance of evidence-based recommendations in the era of whole-genome sequencing: an EGAPP methods update

3 June 2018

1 reference

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Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology.

3 June 2018

1 reference

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Seeking a Coding Solution For Molecular Tests: Managing the estimated 1,700 molecular tests now on the market is impossible without a unique CPT code for each test. What's at stake? The future of personalized medicine.

3 June 2018

1 reference

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The ethical hazards and programmatic challenges of genomic newborn screening

3 June 2018

1 reference

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The n-of-1 clinical trial: the ultimate strategy for individualizing medicine?

3 June 2018

1 reference

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N-of-1 trials in the medical literature: a systematic review

3 June 2018

1 reference

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Carrier testing for severe childhood recessive diseases by next-generation sequencing

3 June 2018

1 reference

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Coverage policy development for personalized medicine: private payer perspectives on developing policy for the 21-gene assay

3 June 2018

1 reference

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Personalized medicine: factors influencing reimbursement.

3 June 2018

1 reference

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Challenges of translating genetic tests into clinical and public health practice

3 June 2018

1 reference

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Pharmacogenomics, evidence, and the role of payers

3 June 2018

1 reference

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The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group

3 June 2018

1 reference

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Evidence-based coverage policy

3 June 2018

1 reference

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Integrating molecular medicine into the US health-care system: opportunities, barriers, and policy challenges.

3 June 2018

1 reference

Crossref

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Genetic tests: Politics and fetal diagnostics collide

21 January 2018

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Insurance coverage for pharmacogenomic testing in the USA

21 January 2018

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Crossref

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Accessing genomic medicine: affordability, diffusion, and disparities

21 January 2018

1 reference

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NCCN molecular testing white paper: effectiveness, efficiency, and reimbursement

26 November 2018

1 reference

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Biomarker development, commercialization, and regulation: individualization of medicine lost in translation

26 November 2018

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Challenges in the clinical application of whole-genome sequencing

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Molecular technologies open new clinical genetic vistas

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Special report: multiple molecular testing of cancers to identify targeted therapies

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Sequencing-based tests to determine fetal down syndrome (trisomy 21) from maternal plasma DNA

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Special report: exome sequencing for clinical diagnosis of patients with suspected genetic disorders

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Genomic pathology: a disruptive innovation

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Modernizing US regulatory and reimbursement policy to support continued innovation in genomic pathology

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The business value and cost-effectiveness of genomic medicine

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Genetic testing insurance coverage trends: a review of publicly available policies from the largest US payers

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Identifiers

DOI

10.1111/JLME.12160

1 reference

20 August 2017

1 reference

20 August 2017

1 reference

PMCID

5108048