Literature DB >> 27127186

The challenge of consent in clinical genome-wide testing.

Katherine Burke1, Angus Clarke1.   

Abstract

Genome-wide testing methods include array comparative genomic hybridisation (aCGH), multiple gene panels, whole exome sequencing (WE) and whole genome sequencing (WGS). Here we introduce some of the key ethical and social considerations relating to informed consent for the testing of children, particularly the management of incidental findings and variants of unknown significance. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

Entities:  

Keywords:  Ethics; General Paediatrics; Genetics; Neonatology

Mesh:

Year:  2016        PMID: 27127186     DOI: 10.1136/archdischild-2013-304109

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  7 in total

1.  The fetus in the age of the genome.

Authors:  Dagmar Schmitz; Wolfram Henn
Journal:  Hum Genet       Date:  2021-08-23       Impact factor: 5.881

2.  Rapid Challenges: Ethics and Genomic Neonatal Intensive Care.

Authors:  Christopher Gyngell; Ainsley J Newson; Dominic Wilkinson; Zornitza Stark; Julian Savulescu
Journal:  Pediatrics       Date:  2019-01       Impact factor: 7.124

3.  Congenital Cataract and Its Genetics: The Era of Next-Generation Sequencing

Authors:  Hande Taylan Şekeroğlu; Gülen Eda Utine
Journal:  Turk J Ophthalmol       Date:  2021-04-29

Review 4.  Informed Consent in the Genomics Era.

Authors:  Shannon Rego; Megan E Grove; Mildred K Cho; Kelly E Ormond
Journal:  Cold Spring Harb Perspect Med       Date:  2020-08-03       Impact factor: 5.159

5.  Shortened consent forms for genome-wide sequencing: Parent and provider perspectives.

Authors:  Emma C Hitchcock; Causes Study; Alison M Elliott
Journal:  Mol Genet Genomic Med       Date:  2020-05-08       Impact factor: 2.183

6.  Share and protect our health data: an evidence based approach to rare disease patients' perspectives on data sharing and data protection - quantitative survey and recommendations.

Authors:  Sandra Courbier; Rebecca Dimond; Virginie Bros-Facer
Journal:  Orphanet J Rare Dis       Date:  2019-07-12       Impact factor: 4.123

7.  Potential and pitfalls in the genetic diagnosis of kidney diseases.

Authors:  Anne Kesselheim; Emma Ashton; Detlef Bockenhauer
Journal:  Clin Kidney J       Date:  2017-07-18
  7 in total

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