(Q35832845)

English

A preliminary investigation of genetic counselors' information needs when receiving a variant of uncertain significance result: a mixed methods study

scientific article published on 8 January 2015

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scholarly article

1 reference

Europe PubMed Central

10 August 2017

A preliminary investigation of genetic counselors' information needs when receiving a variant of uncertain significance result: a mixed methods study (English)

1 reference

Europe PubMed Central

10 August 2017

Fergus J. Couch

4

object named as

Fergus J Couch

1 reference

Europe PubMed Central

10 August 2017

Noralane Lindor

2

object named as

Noralane M Lindor

1 reference

Europe PubMed Central

10 August 2017

author name string

Courtney L Scherr

1

1 reference

Europe PubMed Central

10 August 2017

Teri L Malo

3

1 reference

Europe PubMed Central

10 August 2017

Susan T Vadaparampil

5

1 reference

Europe PubMed Central

10 August 2017

language of work or name

0 references

publication date

8 January 2015

1 reference

Europe PubMed Central

10 August 2017

Genetics in Medicine

1 reference

Europe PubMed Central

10 August 2017

17

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Europe PubMed Central

10 August 2017

9

1 reference

Europe PubMed Central

10 August 2017

739-746

1 reference

Europe PubMed Central

10 August 2017

https://scigraph.springernature.com/pub.10.1038/gim.2014.185

0 references

BRCA1/2 sequence variants of uncertain significance: a primer for providers to assist in discussions and in medical management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

The next controversy in genetic testing: clinical data as trade secrets?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

Translational advances regarding hereditary breast cancer syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

A computational method to classify variants of uncertain significance using functional assay data with application to BRCA1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

Opening the psychological black box in genetic counseling. The psychological impact of DNA testing is predicted by the counselees' perception, the medical impact by the pathogenic or uninformative BRCA1/2-result

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

Comparative effectiveness of screening and prevention strategies among BRCA1/2-affected mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

Hereditary breast cancer: new genetic developments, new therapeutic avenues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

The qualitative content analysis process

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

The counsellees' view of an unclassified variant in BRCA1/2: recall, interpretation, and impact on life.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

The genetic testing process: how much counseling is needed?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

27 July 2018

Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

24 September 2018

NSGC practice guideline: risk assessment and genetic counseling for hereditary breast and ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

24 September 2018

Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

24 September 2018

Variants of uncertain significance in breast cancer-related genes: real-world implications for a clinical conundrum. Part one: clinical genetics recommendations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

24 September 2018

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4496326

24 September 2018

Multigene panel testing: planning the next generation of research studies in clinical cancer genetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/25569439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic/familial high-risk assessment: breast and ovarian, version 1.2014

1 reference

https://pubmed.ncbi.nlm.nih.gov/25569439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical interpretation and recommendations for patients with a variant of uncertain significance in BRCA1 or BRCA2: a survey of genetic counseling practice

1 reference

https://pubmed.ncbi.nlm.nih.gov/25569439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

1 reference

https://pubmed.ncbi.nlm.nih.gov/25569439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/GIM.2014.185

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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