Literature DB >> 16199695

Research for newborn screening: developing a national framework.

Jeffrey R Botkin1.   

Abstract

Newborn metabolic screening represents the largest application of genetic testing in medicine. As new technologies are developed, the number of conditions amenable to newborn screening (NBS) will continue to expand. Despite the scope of these programs, the evidence base for a number of NBS applications remains relatively weak. This article briefly reviews the evidence base for several conditions. The article then develops a proposal for a structured sequence of research protocols to evaluate potential applications for NBS before their formal implementation in public health programs. Such a framework for research will require collaboration between states and the federal government, a collaboration that is emerging through recent federal legislation and funding.

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Year:  2005        PMID: 16199695     DOI: 10.1542/peds.2004-2571

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  15 in total

1.  Policy issues and stakeholder concerns regarding the storage and use of residual newborn dried blood samples for research.

Authors:  Erin Rothwell; Rebecca Anderson; Jeffrey Botkin
Journal:  Policy Polit Nurs Pract       Date:  2010-05-10

Review 2.  Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.

Authors:  Jonathan S Berg; Cynthia M Powell
Journal:  Cold Spring Harb Perspect Med       Date:  2015-10-05       Impact factor: 6.915

3.  Questioning the consensus: managing carrier status results generated by newborn screening.

Authors:  Fiona Alice Miller; Jason Scott Robert; Robin Z Hayeems
Journal:  Am J Public Health       Date:  2008-12-04       Impact factor: 9.308

4.  Clinical and ethical considerations in managing carrier detection.

Authors:  Lainie Friedman Ross; Ellen Wright Clayton
Journal:  Am J Public Health       Date:  2009-06-18       Impact factor: 9.308

5.  Supporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screening.

Authors:  Donald B Bailey; F Daniel Armstrong; Alex R Kemper; Debra Skinner; Steven F Warren
Journal:  J Pediatr Psychol       Date:  2008-03-30

6.  Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project.

Authors:  Debra Skinner; Summer Choudhury; John Sideris; Sonia Guarda; Allen Buansi; Myra Roche; Cynthia Powell; Donald B Bailey
Journal:  Pediatrics       Date:  2011-05-29       Impact factor: 7.124

Review 7.  Newborn screening for galactosaemia.

Authors:  Rohollah Lak; Bahareh Yazdizadeh; Majid Davari; Mojtaba Nouhi; Roya Kelishadi
Journal:  Cochrane Database Syst Rev       Date:  2017-12-23

8.  Parental permission for pilot newborn screening research: guidelines from the NBSTRN.

Authors:  Jeffrey R Botkin; Michelle Huckaby Lewis; Michael S Watson; Kathryn J Swoboda; Rebecca Anderson; Susan A Berry; Natasha Bonhomme; Jeffrey P Brosco; Anne M Comeau; Aaron Goldenberg; Edward Goldman; Bradford Therrell; Jill Levy-Fisch; Beth Tarini; Benjamin Wilfond
Journal:  Pediatrics       Date:  2014-01-06       Impact factor: 7.124

9.  Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.

Authors:  Lawrence D Shriberg; Nancy L Potter; Edythe A Strand
Journal:  J Speech Lang Hear Res       Date:  2010-10-21       Impact factor: 2.297

10.  Lessons that newborn screening in the USA can teach us about biobanking and large-scale genetic studies.

Authors:  Beth A Tarini; John D Lantos
Journal:  Per Med       Date:  2013-01-01       Impact factor: 2.512

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