Literature DB >> 26042913

Newborn screening.

Susan A Berry1.   

Abstract

Newborn screening is a major aspect of public health success. Babies in every state are tested for a recommended uniform screening panel of conditions not otherwise immediately evident in the first days of life. With the goal of reducing morbidity and mortality, conditions should be added to newborn screening panels using a scientific, evidence-based process. Newborn screening is a system involving partners at many levels; neonatologists have a special role in ensuring that their vulnerable patients also receive this life-saving test. Careful attention to the social, legal, and ethical aspects will help increase the scope of newborn screening.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Critical congenital heart disease; Early hearing detection and intervention; Inherited metabolic disorders; Newborn screening

Mesh:

Year:  2015        PMID: 26042913     DOI: 10.1016/j.clp.2015.03.002

Source DB:  PubMed          Journal:  Clin Perinatol        ISSN: 0095-5108            Impact factor:   3.430


  14 in total

1.  Genome Sequencing Technologies and Nursing: What Are the Roles of Nurses and Nurse Scientists?

Authors:  Jacquelyn Y Taylor; Michelle L Wright; Kathleen T Hickey; David E Housman
Journal:  Nurs Res       Date:  2017 Mar/Apr       Impact factor: 2.381

2.  Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result.

Authors:  Anne E Atkins; Beth A Tarini; Emily K Phillips; Amy R U L Calhoun
Journal:  J Community Genet       Date:  2019-02-05

3.  Exome/Genome-Wide Testing in Newborn Screening: A Proportionate Path Forward.

Authors:  Vasiliki Rahimzadeh; Jan M Friedman; Guido de Wert; Bartha M Knoppers
Journal:  Front Genet       Date:  2022-07-04       Impact factor: 4.772

Review 4.  Toxic Metabolites and Inborn Errors of Amino Acid Metabolism: What One Informs about the Other.

Authors:  Namgyu Lee; Dohoon Kim
Journal:  Metabolites       Date:  2022-06-08

5.  Medical genetics and genomic medicine in the United States. Part 2: Reproductive genetics, newborn screening, genetic counseling, training, and registries.

Authors:  Debra S Regier; Carlos R Ferreira; Suzanne Hart; Donald W Hadley; Maximilian Muenke
Journal:  Mol Genet Genomic Med       Date:  2017-11       Impact factor: 2.183

6.  CAP/ACMG proficiency testing for biochemical genetics laboratories: a summary of performance.

Authors:  Devin Oglesbee; Tina M Cowan; Marzia Pasquali; Timothy C Wood; Karen E Weck; Thomas Long; Glenn E Palomaki
Journal:  Genet Med       Date:  2017-06-29       Impact factor: 8.822

7.  Genomic newborn screening: public health policy considerations and recommendations.

Authors:  Jan M Friedman; Martina C Cornel; Aaron J Goldenberg; Karla J Lister; Karine Sénécal; Danya F Vears
Journal:  BMC Med Genomics       Date:  2017-02-21       Impact factor: 3.063

8.  Heel prick test: maternal-fetal conditions that may have an effect on the test results in newborns admitted to the intensive care unit.

Authors:  Letícia Pinto Rodrigues; Sarah Cristina Sato Vaz Tanaka; Vanderlei José Haas; Valéria Cardoso Alves Cunali; Alessandra Bernadete Trovó de Marqui
Journal:  Rev Bras Ter Intensiva       Date:  2019-05-23

9.  Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population.

Authors:  Bin Yu; Wei Long; Yuqi Yang; Ying Wang; Lihua Jiang; Zhengmao Cai; Huaiyan Wang
Journal:  Front Genet       Date:  2018-10-29       Impact factor: 4.599

10.  Application of Next-Generation Sequencing Following Tandem Mass Spectrometry to Expand Newborn Screening for Inborn Errors of Metabolism: A Multicenter Study.

Authors:  Yuqi Yang; Leilei Wang; Benjing Wang; Shuang Liu; Bin Yu; Ting Wang
Journal:  Front Genet       Date:  2019-02-14       Impact factor: 4.599

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