(Q35671138)

9 August 2017

title

Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing (English)

1 reference

9 August 2017

1 reference

Galen Joseph

2

0 references

author name string

Kelly Hitch

1

1 reference

9 August 2017

Jenna Guiltinan

3

1 reference

9 August 2017

Jessica Kianmahd

4

1 reference

9 August 2017

Janey Youngblom

5

1 reference

9 August 2017

Amie Blanco

6

1 reference

9 August 2017

publication date

22 January 2014

1 reference

Journal of Genetic Counseling

9 August 2017

published in

1 reference

9 August 2017

volume

23

1 reference

9 August 2017

issue

4

1 reference

9 August 2017

page(s)

539-551

1 reference

Revealing the complexity of a monogenic disease: rett syndrome exome sequencing

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Implicit essentialism: genetic concepts are implicitly associated with fate concepts

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Methods, challenges, and promise of next-generation sequencing in cancer biology

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Exome sequencing as a tool for Mendelian disease gene discovery

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

What can exome sequencing do for you?

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

The rules remain the same for genomic medicine: the case against "reverse genetic exceptionalism".

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Exome sequencing identifies the cause of a mendelian disorder

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Three approaches to qualitative content analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Impact of genetic testing for Huntington disease on the family system

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Origins of health locus of control beliefs.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Attitudes of African Americans toward return of results from exome and whole genome sequencing.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Defining genes using "blueprint" versus "instruction" metaphors: effects for genetic determinism, response efficacy, and perceived control

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Exome sequencing: a transformative technology

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Consumer perceptions of direct-to-consumer personalized genomic risk assessments

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Evaluating the utility of personal genomic information

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Public expectations for return of results from large-cohort genetic research

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Communicating the results of clinical research to participants: attitudes, practices, and future directions

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Relationships between psychosocial factors and health behavior change in cancer survivors: an integrative review

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Unskilled and unaware of it: how difficulties in recognizing one's own incompetence lead to inflated self-assessments

25 September 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

25 September 2018

https://api.crossref.org/works/10.1007%2FS10897-014-9687-6

Intention to learn results of genetic testing for hereditary colon cancer.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Self-efficacy mechanism in human agency

25 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9687-6

Why People Fail to Recognize Their Own Incompetence

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9687-6

Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9687-6

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

21 January 2018

2 references

https://api.crossref.org/works/10.1007%2FS10897-014-9687-6

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

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

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer

15 November 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9687-6

Integrating next-generation sequencing into the diagnostic testing of inherited cancer predisposition

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4451087

Points to consider in the clinical application of genomic sequencing

15 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24449059

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Predictive genetic testing for hereditary non-polyposis colorectal cancer: uptake and long-term satisfaction

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24449059

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

NCCN clinical practice guidelines in oncology. Colorectal cancer screening

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24449059

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10897-014-9687-6

1 reference

9 August 2017

1 reference

9 August 2017

1 reference