2019
DOI: 10.1002/nav.21882
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Equity in genetic newborn screening

Abstract: This is the author manuscript accepted for publication and has undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as

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Cited by 4 publications
(1 citation statement)
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References 111 publications
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“…16 Today, all US programs use IRT/DNA with few using an expanded DNA panel, which could improve equity for Black and Hispanic children with less common CF DNA variants. 17 As a public health program, NBS should be designed to decrease health care disparities. 18 Incorporating whole genome sequencing into NBS may exacerbate healthcare disparities and should be avoided until we have more diverse racial and ethnic genomic data for conditions included in state NBS panels and a pediatric workforce prepared to counsel families about the actionable and nonactionable findings.…”
mentioning
confidence: 99%
“…16 Today, all US programs use IRT/DNA with few using an expanded DNA panel, which could improve equity for Black and Hispanic children with less common CF DNA variants. 17 As a public health program, NBS should be designed to decrease health care disparities. 18 Incorporating whole genome sequencing into NBS may exacerbate healthcare disparities and should be avoided until we have more diverse racial and ethnic genomic data for conditions included in state NBS panels and a pediatric workforce prepared to counsel families about the actionable and nonactionable findings.…”
mentioning
confidence: 99%