(Q57641888)

English

Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling

scientific article published on 18 November 2014

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

incidental finding

0 references

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

author name string

Jessica Douglas

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

Alicia A Braxton

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

Kate Kramer

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

language of work or name

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publication date

18 November 2014

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Europe PubMed Central

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22 February 2020

number of pages

9

1 reference

based on heuristic

inferred from page(s)

Journal of Genetic Counseling

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

24

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

654-662

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidental findings in clinical genomics: a clarification

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

To know or not to know? Genetic ignorance, autonomy and paternalism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exploring concordance and discordance for return of incidental findings from clinical sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic incidental findings: autonomy regained?

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Technical report: Ethical and policy issues in genetic testing and screening of children

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Challenges in the clinical application of whole-genome sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reporting genomic sequencing results to ordering clinicians: incidental, but not exceptional

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Shared decision making: a path toward improved patient-centered outcomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Laboratory policies on reporting secondary findings in clinical whole exome sequencing: initial uptake of the ACMG's recommendations

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recommendations for returning genomic incidental findings? We need to talk!

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Return of secondary genomic findings vs patient autonomy: implications for medical care

1 reference

https://pubmed.ncbi.nlm.nih.gov/25403901

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10897-014-9794-4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25403901%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

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