(Q37727863)

English

What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research

scientific article published on 09 April 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

0 references

1 reference

Europe PubMed Central

What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

systematic review

1 reference

based on heuristic

inferred from title

author name string

Kim Chivers Seymour

1

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Julia Addington-Hall

2

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Anneke M Lucassen

3

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Claire L Foster

4

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

publication date

9 April 2010

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Journal of Genetic Counseling

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

19

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

330-342

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10897-010-9296-Y

21 January 2018

The genetic epidemiology of BRCA1. Breast Cancer Linkage Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facilitating family communication about predictive genetic testing: probands' perceptions

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Communicating genetic test results to the family: a six-step, skills-building strategy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predictive testing for BRCA1 and 2 mutations: a male contribution

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uptake of hereditary breast/ovarian cancer genetic testing in a French national sample of BRCA1 families. The French Cancer Genetic Network

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accommodating risk: responses to BRCA1/2 genetic testing of women who have had cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Including qualitative research in systematic reviews: opportunities and problems

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Testing for Women Previously Diagnosed with Breast/Ovarian Cancer: Examining the Impact of BRCA1 and BRCA2 Mutation Searching

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Informing one's family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Appraising the evidence: reviewing disparate data systematically

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Whose gene is it? A case discussion about familial conflict over genetic testing for breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parent-child factors and their effect on communicating BRCA1/2 test results to children.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Living with hereditary non-polyposis colorectal cancer; experiences from and impact of genetic testing.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disclosing genetic test results to family members

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

What do we tell the children? Contrasting the disclosure choices of two HD families regarding risk status and predictive genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Experiences of genetic risk: disclosure and the gendering of responsibility.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychological issues among children of hereditary breast cancer gene (BRCA1/2) testing participants

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic attributable risk of breast and ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Social separation" among women under 40 years of age diagnosed with breast cancer and carrying a BRCA1 or BRCA2 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental communication of BRCA1/2 genetic test results to children

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Qualitative research in systematic reviews. Has established a place for itself

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of systematic review methods to qualitative research: practical issues

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer patients who experienced diagnostic genetic testing for cancer susceptibility: reactions and behavior after the disclosure of a positive test result.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The impact of proband mediated information dissemination in families with a BRCA1/2 gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Motivations and psychosocial impact of genetic testing for HNPCC.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How families communicate about HNPCC genetic testing: Findings from a qualitative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An evaluation of needs of female BRCA1 and BRCA2 carriers undergoing genetic counselling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uptake rates for breast cancer genetic testing: a systematic review

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Communication about genetic testing in families of male BRCA1/2 carriers and non-carriers: patterns, priorities and problems

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

All in the family: evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A social network analysis of communication about hereditary nonpolyposis colorectal cancer genetic testing and family functioning

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/20379768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10897-010-9296-Y

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 August 2017

ResearchGate publication ID

0 references

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