(Q38731962)

5 September 2017

Expect the unexpected: screening for secondary findings in clinical genomics research (English)

1 reference

5 September 2017

1 reference

Michael P Mackley

1

1 reference

PubMed ID

28398474

5 September 2017

Benjamin Capps

series ordinal

2

1 reference

5 September 2017

7 April 2017

1 reference

5 September 2017

British Medical Bulletin

1 reference

5 September 2017

122

1 reference

5 September 2017

1

1 reference

5 September 2017

109-122

1 reference

Incidental findings in imaging diagnostic tests: a systematic review

5 September 2017

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Incidentalomas in genomics and radiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

A case report of an incidental finding of a 46,XX, SRY-negative male with masculine phenotype during standard fertility workup with review of the literature and proposed immediate and long-term management guidance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Defining and managing incidental findings in genetic and genomic practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Whole genome scanning: resolving clinical diagnosis and management amidst complex data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Managing incidental findings in human subjects research: analysis and recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Understanding incidental findings in the context of genetics and genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

The incidentalome: a threat to genomic medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Research ethics recommendations for whole-genome research: consensus statement

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Genomic research and incidental findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Incidental findings in genetics research using archived DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

The return of individual research findings in paediatric genetic research

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Ethical implications of the use of whole genome methods in medical research

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Incidental findings from clinical genome-wide sequencing: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Return of genetic testing results in the era of whole-genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

The unintended implications of blurring the line between research and clinical care in a genomic age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Clinical genomic database

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Targeted NGS meets expert clinical characterization: Efficient diagnosis of spastic paraplegia type 11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Processes and factors involved in decisions regarding return of incidental genomic findings in research

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Return of results: towards a lexicon?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

A more fitting term in the incidental findings debate: one term does not fit all situations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Informed consent for human genetic and genomic studies: a systematic review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Are physicians prepared for whole genome sequencing? a qualitative analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Aggregate penetrance of genomic variants for actionable disorders in European and African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Incidental variants are critical for genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

An incidental finding of a large genomic deletion of BRCA1 on a molecular karyotype for a 5 year old child

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

Policy challenges of clinical genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDX009

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/10.1093%2FBMB%2FLDX009

21 January 2018

Identifiers

DOI

10.1093/BMB/LDX009

1 reference

5 September 2017

1 reference

PubMed ID

28398474