A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system-Reference-Cited by-同舟云学术

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A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system

Published:2019-02-18 Issue:2 Volume:28 Page:388-397
ISSN:1059-7700
Container-title:Journal of Genetic Counseling
language:en
Short-container-title:J Genet Couns

Author:

Martyn Melissa¹²³,Kanga-Parabia Anaita¹²³,Lynch Elly¹³⁴,James Paul A.⁵⁶,Macciocca Ivan³⁴,Trainer Alison H.⁵⁶,Halliday Jane²³,Keogh Louise²,Wale Janney¹,Winship Ingrid⁶,Bogwitz Michael⁶,Valente Giulia⁷,Walsh Maie⁵⁶,Downie Lilian²³⁴,Amor David²⁸,Wallis Mathew⁷,Cunningham Fiona³⁹,Burgess Matthew⁷,Brown Natasha J.²³⁴⁷⁸,Jarmolowicz Anna³⁴,Lunke Sebastian³⁴,Goranitis Ilias²³,Gaff Clara L.¹²³,

Affiliation:

1. Melbourne Genomics Health Alliance; Melbourne Australia

2. University of Melbourne; Melbourne Australia

3. Murdoch Children’s Research Institute; Melbourne Australia

4. Victorian Clinical Genetics Services; Melbourne Australia

5. Peter MacCallum Cancer Institute; Melbourne Australia

6. The Royal Melbourne Hospital; Melbourne Australia

7. Austin Health; Melbourne Australia

8. Royal Children’s Hospital; Melbourne Australia

9. Monash Health; Melbourne Australia

Publisher

Wiley

Subject

Genetics(clinical)

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jgc4.1102/fullpdf

Reference40 articles.

1. Understanding variations in secondary findings reporting practices across US genome sequencing laboratories;Ackerman;AJOB Empirical Bioethics,2018

2. ACMG policy statement: Updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing;ACMG Board of Directors;Genetics in Medicine,2015

3. Bennett , B. 2017 What does consent mean for Generation Genome? http://www.bionews.org.uk/page_886840.asp

4. Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time;Berg;Genetics in Medicine,2011

5. Informed consent for exome sequencing research in families with genetic disease: The emerging issue of incidental findings;Bergner;American Journal of Medical Genetics Part A,2014

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Evaluation of a two-step model of opportunistic genomic screening;European Journal of Human Genetics;2024-03-25

2. Eliciting parental preferences and values for the return of additional findings from genomic sequencing;npj Genomic Medicine;2024-02-14

3. Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol;BMJ Open;2023-06

4. Offering and Returning Secondary Findings in the Context of Exome Sequencing for Hearing Loss: Clinicians’ Views and Experiences;AJOB Empirical Bioethics;2023-01-03

5. Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics Study;Genes;2022-10-06

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