(Q46568709)

23 December 2017

title

Reporting genomic secondary findings: ACMG members weigh in. (English)

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23 December 2017

author name string

Maren T Scheuner

1

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23 December 2017

Jane Peredo

2

1 reference

23 December 2017

Judith Benkendorf

3

1 reference

23 December 2017

Bruce Bowdish

4

1 reference

23 December 2017

Gerald Feldman

5

1 reference

23 December 2017

Lynn Fleisher

6

1 reference

23 December 2017

John J Mulvihill

7

1 reference

23 December 2017

Michael Watson

8

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23 December 2017

Gail E Herman

9

1 reference

23 December 2017

James Evans

10

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23 December 2017

language of work or name

English

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publication date

13 November 2014

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23 December 2017

published in

Genetics in Medicine

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23 December 2017

volume

17

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23 December 2017

issue

1

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23 December 2017

page(s)

27-35

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23 December 2017

https://scigraph.springernature.com/pub.10.1038/gim.2014.165

exact match

0 references

cites work

Implementing genomic medicine in the clinic: the future is here

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Diagnostic clinical genome and exome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Next-generation sequencing identifies rare variants associated with Noonan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Mutations in EMP2 cause childhood-onset nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Novel genomic techniques open new avenues in the analysis of monogenic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Views of genetics health professionals on the return of genomic results.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Views of primary care providers regarding the return of genome sequencing incidental findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Genetics in health care: an overview of current and emerging models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.165

Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25394173

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Points to consider in the clinical application of genomic sequencing

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25394173

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Anticipate and communicate: Ethical management of incidental and secondary findings in the clinical, research, and direct-to-consumer contexts (December 2013 report of the Presidential Commission for the Study of Bioethical Issues).

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25394173

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/GIM.2014.165

1 reference

23 December 2017

1 reference

23 December 2017