(Q33555443)

English

Hereditary nonpolyposis colorectal cancer family members' perceptions about the duty to inform and health professionals' role in disseminating genetic information

scientific article

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Hereditary nonpolyposis colorectal cancer family members' perceptions about the duty to inform and health professionals' role in disseminating genetic information (English)

1 reference

Europe PubMed Central

28 July 2017

colorectal cancer

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

colorectal carcinoma

1 reference

based on heuristic

inferred from title

7

object named as

Ellen R Gritz

1 reference

Europe PubMed Central

28 July 2017

Rebecca D. Pentz

1

object named as

Rebecca D Pentz

1 reference

Europe PubMed Central

28 July 2017

6

object named as

Laura M Koehly

1 reference

Europe PubMed Central

28 July 2017

author name string

Susan K Peterson

2

1 reference

Europe PubMed Central

28 July 2017

Beatty Watts

3

1 reference

Europe PubMed Central

28 July 2017

Sally W Vernon

4

1 reference

Europe PubMed Central

28 July 2017

Patrick M Lynch

5

1 reference

Europe PubMed Central

28 July 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 January 2005

1 reference

Europe PubMed Central

28 July 2017

Genetic Testing and Molecular Biomarkers

1 reference

Europe PubMed Central

28 July 2017

9

1 reference

Europe PubMed Central

28 July 2017

3

1 reference

Europe PubMed Central

28 July 2017

261-268

1 reference

Europe PubMed Central

28 July 2017

Family communication about genetic risk: the little that is known

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

Concern for families and individuals in clinical genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

The family covenant and genetic testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

Cancer risk in mutation carriers of DNA-mismatch-repair genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

Attitudes towards cancer predictive testing and transmission of information to the family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

21 June 2018

Psychological impact of genetic testing for hereditary nonpolyposis colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Duty to warn about hereditary disease risks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

We are talking, but are they listening? Communication patterns in families with a history of breast/ovarian cancer (HBOC).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

The adverse effects of HIPAA on patient care.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Genetic information and the family: are we our brother's keeper?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Diffusion of information about genetic risk within families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Rethinking medical confidentiality: the impact of genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Attitudes and interest in genetic testing for breast and ovarian cancer susceptibility in diverse groups of women in western Washington.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Familial disclosure in defiance of nonconsent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Design and methodology of a study of psychosocial aspects of genetic testing for hereditary colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Patients' attitudes about autonomy and confidentiality in genetic testing for breast-ovarian cancer susceptibility.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Trust, The fragile foundation of contemporary biomedical research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

Measures of family functioning for research and practice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007282

31 October 2018

ASHG statement. Professional disclosure of familial genetic information. The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family Communication and Genetic Counseling: The Case of Hereditary Breast and Ovarian Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The "duty to warn" a patient's family members about hereditary disease risks

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Medical Geneticists' duty to warn at-risk relatives for genetic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disclosure of familial genetic information: perceptions of the duty to inform

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disclosure to the family of breast/ovarian cancer genetic test results: patient's willingness and associated factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

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/16225406

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/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Community involvement in developing policies for genetic testing: assessing the interests and experiences of individuals affected by genetic conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16225406

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1089/GTE.2005.9.261

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

ResearchGate publication ID

0 references

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