US private payers’ perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER)-Reference-Cited by-同舟云学术

US private payers’ perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER)

Published:2022-01 Issue:1 Volume:24 Page:238-244
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Phillips Kathryn A.,Trosman Julia R.,Douglas Michael P.,Gelb Bruce D.,Ferket Bart S.,Hindorff Lucia A.,Slavotinek Anne M.,Berg Jonathan S.,Russell Heidi V.,Devine Beth,Greve Veronica,Smith Hadley Stevens

Funder

National Human Genome Research Institute

National Cancer Institute

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference12 articles.

1. Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases;Clark;NPJ Genom Med,2018

2. A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants;Kingsmore;Am J Hum Genet,2019

3. Expanding Use of Clinical Genome Sequencing and the Need for More Data on Implementation;Phillips;JAMA,2020

4. Availability and funding of clinical genomic sequencing globally;Phillips;BMJ Glob Health,2021

5. 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);Trosman;Genet Med,2020

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3. Genomic approaches to rare disorder diagnosis;Comprehensive Precision Medicine;2024

4. Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US;Prenatal Diagnosis;2023-09-26

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