Literature DB >> 21407080

Secretary's Advisory Committee on Heritable Disorders in Newborns and Children response to the President's Council on Bioethics report: the changing moral focus of newborn screening.

Tracy L Trotter1, Alan R Fleischman, R Rodney Howell, Michele Lloyd-Puryear.   

Abstract

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Year:  2011        PMID： 21407080     DOI： 10.1097/GIM.0b013e318210655d

Source DB:  PubMed          Journal:  Genet Med        ISSN： 1098-3600            Impact factor:   8.822


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  5 in total

1.  Genetics and bioethics: how our thinking has changed since 1969.

Authors:  LeRoy Walters
Journal:  Theor Med Bioeth       Date:  2012-02

Review 2.  Changing trends in carrier screening for genetic disease in the United States.

Authors:  Shivani B Nazareth; Gabriel A Lazarin; James D Goldberg
Journal:  Prenat Diagn       Date:  2015-07-27       Impact factor: 3.050

3.  "We needed this": perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy.

Authors:  Didu S T Kariyawasam; Arlene M D'Silva; Janine Vetsch; Claire E Wakefield; Veronica Wiley; Michelle A Farrar
Journal:  EClinicalMedicine       Date:  2021-02-19

Review 4.  Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations.

Authors:  Kimberly Shoenbill; Norman Fost; Umberto Tachinardi; Eneida A Mendonca
Journal:  J Am Med Inform Assoc       Date:  2013-06-14       Impact factor: 4.497

Review 5.  The Use of Whole Genome and Exome Sequencing for Newborn Screening: Challenges and Opportunities for Population Health.

Authors:  Audrey C Woerner; Renata C Gallagher; Jerry Vockley; Aashish N Adhikari
Journal:  Front Pediatr       Date:  2021-07-19       Impact factor: 3.418
  5 in total

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