(Q37102122)

18 August 2017

Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk (English)

1 reference

18 August 2017

7

Bartha M Knoppers

1 reference

18 August 2017

8

Denise Avard

1 reference

18 August 2017

6

Jacques Simard

1 reference

18 August 2017

2

Erika Kleiderman

1 reference

18 August 2017

1

Kelly A McClellan

1 reference

18 August 2017

Lee Black

3

1 reference

18 August 2017

Karine Bouchard

series ordinal

4

1 reference

18 August 2017

Michel Dorval

series ordinal

5

1 reference

18 August 2017

23 January 2013

1 reference

European Journal of Human Genetics

18 August 2017

1 reference

18 August 2017

21

1 reference

18 August 2017

9

1 reference

18 August 2017

903-910

1 reference

Whole-genome and whole-exome sequencing in hereditary cancer: impact on genetic testing and counseling

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Erratum to: A short history of the first three years of the Community Genetics Network and its Newsletter

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

A short history of the first 3 years of the Community Genetics Network and its newsletter

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Unpacking the blockers: understanding perceptions and social constraints of health communication in hereditary breast ovarian cancer (HBOC) susceptibility families

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Factors determining dissemination of results and uptake of genetic testing in families with known BRCA1/2 mutations

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Breast cancer risk reduction and counseling: lifestyle, chemoprevention, and surgery

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Women receiving news of a family BRCA1/2 mutation: messages of fear and empowerment.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Communication of BRCA1 and BRCA2 results to at‐risk relatives: A cancer risk assessment program's experience

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Characteristics of health information gatherers, disseminators, and blockers within families at risk of hereditary cancer: implications for family health communication interventions.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Unambiguous test results or individual independence? The role of clients and families in predictive BRCA-testing in the Netherlands compared to the USA.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Intention to communicate BRCA1/BRCA2 genetic test results to the family

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

Sharing BRCA1/2 test results with first-degree relatives: factors predicting who women tell.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746262

To tell or not to tell: barriers and facilitators in family communication about genetic risk

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.286

‘It's their blood not mine’: Who's responsible for (not) telling relatives about genetic risk?

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2012.286

Life events may contribute to family communication about cancer risk following BRCA1/2 testing

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23340514

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic counseling and the advanced practice oncology nursing role in a hereditary cancer prevention clinic: hereditary breast cancer focus (part I)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23340514

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2012.286

1 reference

Dimensions Publication ID

18 August 2017

0 references

1 reference

18 August 2017

PubMed publication ID

23340514

1 reference