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Including ELSI research questions in newborn screening pilot studies

Genetics in medicine, 2019-03, Vol.21 (3), p.525-533

2019

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Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children

Genetics in medicine, 2014-02, Vol.16 (2), p.183-187

2014

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Foundation of the Newborn Screening Translational Research Network and its tools for research

Genetics in medicine, 2019-06, Vol.21 (6), p.1271-1279

2019

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Newborn screening: toward a uniform screening panel and system

Genetics in medicine, 2006-05, Vol.8 Suppl 1, p.1S-252S

2006

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Health-care providers’ perspectives on uncertainty generated by variant forms of newborn screening targets

Genetics in medicine, 2020-03, Vol.22 (3), p.566-573

2020

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Revisiting the Wilson-Jungner criteria: how can supplemental criteria guide public health in the era of genetic screening?

Genetics in medicine, 2012-01, Vol.14 (1), p.129-134

Petros, Michael

2012

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Laboratory analysis of amino acids, 2018 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2018-12, Vol.20 (12), p.1499-1507

2018

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Damaged goods?: an empirical cohort study of blood specimens collected 12 to 23 hours after birth in newborn screening in California

Genetics in medicine, 2016-03, Vol.18 (3), p.259-264

2016

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Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening

Genetics in medicine, 2011-07, Vol.13 (7), p.621-624

2011

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Technical standards and guidelines for the diagnosis of biotinidase deficiency

Genetics in medicine, 2010-07, Vol.12 (7), p.464-470

2010

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What is the role of clinical genetics in the patient-centered medical home?: A commentary from the Medical Home Workgroup of the Heartland Regional Genetics and Newborn Screening Collaborative

Genetics in medicine, 2016-05, Vol.18 (5), p.440-442

2016

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Storage and use of residual newborn screening blood spots: A public policy emergency

Genetics in medicine, 2011-07, Vol.13 (7), p.619-620

Tarini, Beth A.

2011

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Weighing the evidence for newborn screening for early-infantile Krabbe disease

Genetics in medicine, 2010-09, Vol.12 (9), p.539-543

2010

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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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Impact of false-positive newborn metabolic screening results on early health care utilization

Genetics in medicine, 2009-10, Vol.11 (10), p.716-721

2009

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Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and recommendations from the Secretary of Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children

Genetics in medicine, 2013-03, Vol.15 (3), p.229-233

2013

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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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Optimizing Bob Guthrie's legacy—Storage and use of residual newborn screening specimens

Genetics in medicine, 2011-07, Vol.13 (7), p.617-618

Webster, Dianne

2011

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Committee Report: advancing the current recommended panel of conditions for newborn screening

Genetics in medicine, 2007-11, Vol.9 (11), p.792-796

2007

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Quality improvement of newborn screening in real time

Genetics in medicine, 2011-03, Vol.13 (3), p.205-205

Howell, R Rodney

2011

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Newborn dried bloodspot screening: mapping the clinical and public health components and activities

Genetics in medicine, 2009-06, Vol.11 (6), p.418-424

2009

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Developing a National Registry for conditions identifiable through newborn screening

Genetics in medicine, 2009-03, Vol.11 (3), p.176-182

2009

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Diagnostic guidelines for newborns who screen positive in newborn screening

Genetics in medicine, 2010-12, Vol.12 (12 Suppl), p.S251-S255

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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Newborn screening as a system from birth through lifelong care

Genetics in medicine, 2009-06, Vol.11 (6), p.409-410

2009

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Including ELSI research questions in newborn screening pilot studies

Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children

Foundation of the Newborn Screening Translational Research Network and its tools for research

Newborn screening: toward a uniform screening panel and system

Health-care providers’ perspectives on uncertainty generated by variant forms of newborn screening targets

Revisiting the Wilson-Jungner criteria: how can supplemental criteria guide public health in the era of genetic screening?

Laboratory analysis of amino acids, 2018 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)

Damaged goods?: an empirical cohort study of blood specimens collected 12 to 23 hours after birth in newborn screening in California

Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening

Technical standards and guidelines for the diagnosis of biotinidase deficiency

What is the role of clinical genetics in the patient-centered medical home?: A commentary from the Medical Home Workgroup of the Heartland Regional Genetics and Newborn Screening Collaborative

Storage and use of residual newborn screening blood spots: A public policy emergency

Weighing the evidence for newborn screening for early-infantile Krabbe disease

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

Impact of false-positive newborn metabolic screening results on early health care utilization

Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and recommendations from the Secretary of Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children

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

Optimizing Bob Guthrie's legacy—Storage and use of residual newborn screening specimens

Committee Report: advancing the current recommended panel of conditions for newborn screening

Quality improvement of newborn screening in real time

Newborn dried bloodspot screening: mapping the clinical and public health components and activities

Developing a National Registry for conditions identifiable through newborn screening

Diagnostic guidelines for newborns who screen positive in newborn screening

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

Newborn screening as a system from birth through lifelong care

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