(Q57142370)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

title

Ethical signposts for clinical geneticists in secondary variant and incidental finding disclosure discussions (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

0 references

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

author name string

Gabrielle M Christenhusz

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Koenraad Devriendt

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

Hilde Van Esch

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

language of work or name

English

0 references

publication date

1 August 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

Medicine Health Care and Philosophy

23 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

volume

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

page(s)

361-370

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s11019-014-9611-8

23 February 2020

exact match

0 references

cites work

Disclosure of individual genetic data to research participants: the debate reconsidered

1 reference

12 December 2020

Returning pleiotropic results from genetic testing to patients and research participants

1 reference

12 December 2020

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

1 reference

12 December 2020

GIG response to the UK Clinical Genetics Society report "The genetic testing of children"

1 reference

12 December 2020

Value neutrality and nondirectiveness: comments on "Future directions in genetic counseling

1 reference

12 December 2020

Secondary variants--in defense of a more fitting term in the incidental findings debate.

1 reference

12 December 2020

Next-generation DNA sequencing methods

1 reference

12 December 2020

Recognizing tacit knowledge in medical epistemology.

1 reference

12 December 2020

The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practice

1 reference

12 December 2020

Personalized genomic medicine and the rhetoric of empowerment

1 reference

12 December 2020

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

1 reference

12 December 2020

Managing incidental findings in human subjects research: analysis and recommendations

1 reference

12 December 2020

The indispensable role of professional judgment in genomic medicine

1 reference

12 December 2020

Incidental findings in human subjects research: what do investigators owe research participants?

1 reference

12 December 2020

Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: a global problem

1 reference

12 December 2020

Patient autonomy and value-neutrality in nondirective genetic counseling.

1 reference

12 December 2020

Predicting preferences: a neglected aspect of shared decision-making

1 reference

12 December 2020

Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation

1 reference

12 December 2020

How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

1 reference

12 December 2020

What is the role of empirical research in bioethical reflection and decision-making? An ethical analysis

1 reference

12 December 2020

Incidentalomas in genomics and radiology

1 reference

12 December 2020

The "right not to know" in the genomic era: time to break from tradition?

1 reference

12 December 2020

Characterizing genetic variants for clinical action

1 reference

12 December 2020

Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy

1 reference

12 December 2020

The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical care.

1 reference

12 December 2020

“I want to know what's in Pandora's box”: Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing

1 reference

12 December 2020

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

1 reference

12 December 2020

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

1 reference

12 December 2020

Psychological Model for Presymptomatic Test Interviews: Lessons Learned from Huntington Disease

1 reference

12 December 2020

Human genetic research: emerging trends in ethics

1 reference

12 December 2020

Why genomics shouldn't get too personal: in favor of filters: Re: invited comment by Holly K. Tabor et al. in American Journal of Medical Genetics Part A Volume 155

1 reference

12 December 2020

'You don't make genetic test decisions from one day to the next'--using time to preserve moral space

1 reference

12 December 2020

The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing.

1 reference

12 December 2020

The future in clinical genetics: affective forecasting biases in patient and clinician decision making

1 reference

12 December 2020

Informed decision making about predictive DNA tests: arguments for more public visibility of personal deliberations about the good life

1 reference

12 December 2020

The behavioral response to personalized genetic information: will genetic risk profiles motivate individuals and families to choose more healthful behaviors?

1 reference

12 December 2020

Introduction: the challenge of incidental findings

1 reference

12 December 2020

The many faces of competency.

1 reference

12 December 2020

How could disclosing incidental information from whole-genome sequencing affect patient behavior?

1 reference

12 December 2020

To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.

1 reference

12 December 2020

Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).

1 reference

12 December 2020

Gene concepts and genethics: beyond exceptionalism.

1 reference

12 December 2020

Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies

1 reference

12 December 2020

Multidimensional results reporting to participants in genomic studies: getting it right.

1 reference

12 December 2020

Genetic information: a joint account?

1 reference

12 December 2020

Family Resilience: A Framework for Clinical Practice

1 reference

12 December 2020

Evaluating the utility of personal genomic information

1 reference

12 December 2020

Dynamic consent: a patient interface for twenty-first century research networks

1 reference

12 December 2020

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

12 December 2020

Genetic information in the age of genohype.

1 reference

12 December 2020

Reconceiving the family. The process of consent in medical decisionmaking.

1 reference

12 December 2020

Disclosing incidental findings in genetics contexts: a review of the empirical ethical research

1 reference

12 December 2020

Risk detection in individual health care: any limits?

1 reference

12 December 2020

Personal utility and genomic information: look before you leap

1 reference

12 December 2020

Toward a biopsychosocial model for 21st-century genetics

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S11019-014-9611-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25407129%20AND%20SRC:MED&resulttype=core&format=json

23 February 2020

1 reference