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We screen newborns, don't we?: realizing the promise of public health genomics

Genetics in medicine, 2013-05, Vol.15 (5), p.332-334

2013

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Neonatal screening for congenital adrenal hyperplasia

Nature reviews. Endocrinology, 2009-09, Vol.5 (9), p.490-498

White, Perrin C

2009

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A novel, more efficient, staged approach for critical congenital heart disease screening

Journal of perinatology, 2017-03, Vol.37 (3), p.288-290

2017

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Reduction in newborn screening metabolic false-positive results following a new collection protocol

Genetics in medicine, 2014-06, Vol.16 (6), p.477-483

2014

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A framework for key considerations regarding point-of-care screening of newborns

Genetics in medicine, 2012-12, Vol.14 (12), p.951-954

2012

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Evaluation of pulse oximetry screening in Middle Tennessee: cases for consideration before universal screening

Journal of perinatology, 2011-02, Vol.31 (2), p.125-129

Walsh, W

2011

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Neuromuscular disease: Muscular dystrophy--something new on God's green earth?

Nature reviews. Neurology, 2012-05, Vol.8 (5), p.247

Ferlini, Alessandra

2012

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Newborn screening residual dried blood spot use for newborn screening quality improvement

Genetics in medicine, 2010-12, Vol.12 (12 Suppl), p.S269-S272

2010

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Exploring barriers to long-term follow-up in newborn screening programs

Genetics in medicine, 2006-09, Vol.8 (9), p.563-570

2006

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Screen savers

Nature medicine, 2005-10, Vol.11 (10), p.1020

Mandavilli, Apoorva

2005

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Impact of family health insurance and other environmental factors on universal hearing screen program effectiveness

Journal of perinatology, 2002-07, Vol.22 (5), p.380-385

2002

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Video-call based newborn triage system for local birth centres can be established without major instalment costs using commercially available smartphones

Scientific reports, 2020-05, Vol.10 (1), p.7552-7552, Article 7552

2020

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Evaluation of the economic impact of modified screening criteria for retinopathy of prematurity from the Postnatal Growth and ROP (G-ROP) study

Journal of perinatology, 2020-07, Vol.40 (7), p.1100-1108

2020

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Newborn screening 50 years later: access issues faced by adults with PKU

Genetics in medicine, 2013-08, Vol.15 (8), p.591-599

2013

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Public views on participating in newborn screening using genome sequencing

European journal of human genetics : EJHG, 2014-11, Vol.22 (11), p.1248-1254

2014

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Insurance coverage of medical foods for treatment of inherited metabolic disorders

Genetics in medicine, 2013-12, Vol.15 (12), p.978-982

2013

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A cost-effectiveness analysis of maternal CYP2D6 genetic testing to guide treatment for postpartum pain and avert infant adverse events

The pharmacogenomics journal, 2018-05, Vol.18 (3), p.391-397

2018

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Newborn screening programs: Should 22q11 deletion syndrome be added?

Genetics in medicine, 2010-03, Vol.12 (3), p.135-144

2010

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Emotional distress in mothers of preterm hospitalized infants: a feasibility trial of nurse-delivered treatment

Journal of perinatology, 2013-12, Vol.33 (12), p.924-928

2013

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Research use of leftover newborn bloodspots: attitudes of Canadian geneticists regarding storage and informed consent requirements

Genetics in medicine, 2011-04, Vol.13 (4), p.305-313

2011

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Outcome and cost analysis of implementing selective Coombs testing in the newborn nursery

Journal of perinatology, 2012-12, Vol.32 (12), p.966-969

2012

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Newborn hearing screening: costs of establishing a program

Journal of perinatology, 2002-03, Vol.22 (2), p.120-124

2002

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Tandem mass spectrometry in newborn screening. American College of Medical Genetics/American Society of Human Genetics Test and Technology Transfer Committee Working Group

Genetics in medicine, 2000-07, Vol.2 (4), p.267-269

American College of Medical Genetics/American Society of Human Genetics Test and Technology Transfer Committee Working Group

2000

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Genetic services in The Netherlands

European journal of human genetics : EJHG, 1997, Vol.5 Suppl 2 (Suppl. 2), p.125-129

ten Kate, L P

1997

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We screen newborns, don't we?: realizing the promise of public health genomics

Neonatal screening for congenital adrenal hyperplasia

A novel, more efficient, staged approach for critical congenital heart disease screening

Reduction in newborn screening metabolic false-positive results following a new collection protocol

A framework for key considerations regarding point-of-care screening of newborns

Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study

Evaluation of pulse oximetry screening in Middle Tennessee: cases for consideration before universal screening

Neuromuscular disease: Muscular dystrophy--something new on God's green earth?

Newborn screening residual dried blood spot use for newborn screening quality improvement

Exploring barriers to long-term follow-up in newborn screening programs

Screen savers

Impact of family health insurance and other environmental factors on universal hearing screen program effectiveness

Video-call based newborn triage system for local birth centres can be established without major instalment costs using commercially available smartphones

Evaluation of the economic impact of modified screening criteria for retinopathy of prematurity from the Postnatal Growth and ROP (G-ROP) study

Newborn screening 50 years later: access issues faced by adults with PKU

Public views on participating in newborn screening using genome sequencing

Insurance coverage of medical foods for treatment of inherited metabolic disorders

A cost-effectiveness analysis of maternal CYP2D6 genetic testing to guide treatment for postpartum pain and avert infant adverse events

Newborn screening programs: Should 22q11 deletion syndrome be added?

Emotional distress in mothers of preterm hospitalized infants: a feasibility trial of nurse-delivered treatment

Research use of leftover newborn bloodspots: attitudes of Canadian geneticists regarding storage and informed consent requirements

Outcome and cost analysis of implementing selective Coombs testing in the newborn nursery

Newborn hearing screening: costs of establishing a program

Tandem mass spectrometry in newborn screening. American College of Medical Genetics/American Society of Human Genetics Test and Technology Transfer Committee Working Group

Genetic services in The Netherlands

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