(Q26777211)

Current genetic medicine reports

published in

1 reference

Creative Commons Attribution 4.0 International

volume

3

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issue

4

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page(s)

166-176

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copyright license

start time

25 August 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Decision aids for people facing health treatment or screening decisions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Do researchers have an obligation to actively look for genetic incidental findings?

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

A systematic approach to the reporting of medically relevant findings from whole genome sequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Parents are interested in newborn genomic testing during the early postpartum period

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Clinical exome performance for reporting secondary genetic findings

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Molecular findings among patients referred for clinical whole-exome sequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Effect of enhanced information, values clarification, and removal of financial barriers on use of prenatal genetic testing: a randomized clinical trial

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Genetic information, non-discrimination, and privacy protections in genetic counseling practice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Models of consent to return of incidental findings in genomic research

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Interactive e-counselling for genetics pre-test decisions: where are we now?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Return of genomic results to research participants: the floor, the ceiling, and the choices in between

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Seeking Genomic Knowledge: The Case for Clinical Restraint

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Return of results: ethical and legal distinctions between research and clinical care

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

An assessment of time involved in pre-test case review and counseling for a whole genome sequencing clinical research program

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Public views on participating in newborn screening using genome sequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Returning pleiotropic results from genetic testing to patients and research participants

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Actionable, pathogenic incidental findings in 1,000 participants' exomes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Ethical, legal, and social implications of incorporating genomic information into electronic health records

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Point-counterpoint. Ethics and genomic incidental findings

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

'Information is information': a public perspective on incidental findings in clinical and research genome-based testing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

The indispensable role of professional judgment in genomic medicine

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Managing incidental genomic findings: legal obligations of clinicians

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Disclosure of incidental findings from next-generation sequencing in pediatric genomic research

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Approaches to informed consent for hypothesis-testing and hypothesis-generating clinical genomics research

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

An informatics approach to analyzing the incidentalome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Effects of informed consent for individual genome sequencing on relevant knowledge

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

The past, present, and future of the debate over return of research results and incidental findings

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Whole exome and whole genome sequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Disclosure of APOE genotype for risk of Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Managing incidental findings in human subjects research: analysis and recommendations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

A systematic review of perceived risks, psychological and behavioral impacts of genetic testing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

The incidentalome: a threat to genomic medicine

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

The right not to know: an autonomy based approach

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 September 2017

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

The impact of reporting incidental findings from exome and whole-genome sequencing: predicted frequencies based on modeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

When is a medical finding "incidental"?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Addressing the ethical challenges in genetic testing and sequencing of children

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Reporting genomic secondary findings: ACMG members weigh in.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Incidental findings in clinical genomics: a clarification

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Points to consider for informed consent for genome/exome sequencing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Points to consider in the clinical use of NGS panels for mitochondrial disease: an analysis of gene inclusion and consent forms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Practices and policies of clinical exome sequencing providers: analysis and implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Ethical and policy issues in genetic testing and screening of children

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Patients' views on incidental findings from clinical exome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Investing in deliberation: a definition and classification of decision support interventions for people facing difficult health decisions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

New challenges for informed consent through whole genome array testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Paternalism and the ACMG recommendations on genomic incidental findings: patients seen but not heard

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Incidental findings in genetic research and clinical diagnostic tests: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

Experiences with obtaining informed consent for genomic sequencing.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Focus group discussions on secondary variants and next-generation sequencing technologies.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

The hidden harm behind the return of results from personal genome services: a need for rigorous and responsible evaluation

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4633435

Challenges in the clinical application of whole-genome sequencing

28 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/26566463

12 December 2020

inferred from PubMed ID database lookup

Moving toward NextGenetic counseling

1 reference

https://pubmed.ncbi.nlm.nih.gov/26566463

12 December 2020

inferred from PubMed ID database lookup

Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?

1 reference

https://pubmed.ncbi.nlm.nih.gov/26566463

12 December 2020

inferred from PubMed ID database lookup

Subtle Psychosocial Sequelae of Genetic Test Results

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

7 January 2021

inferred from DOI database lookup

Reporting Incidental Findings in Genomic Scale Clinical Sequencing-A Clinical Laboratory Perspective: A Report of the Association for Molecular Pathology

1 reference

https://api.crossref.org/works/10.1007%2FS40142-015-0075-9

7 January 2021