(Q33780087)

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Patient responses to genetic information: studies of patients with hereditary cancer syndromes identify issues for use of genetic testing in nephrology practice

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

Europe PubMed Central

Patient responses to genetic information: studies of patients with hereditary cancer syndromes identify issues for use of genetic testing in nephrology practice (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Kimberly A Kaphingst

1

object named as

Kimberly A Kaphingst

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Colleen M McBride

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

publication date

1 March 2010

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Seminars in Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

30

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

203-214

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Colorectal cancer risk perception on the basis of genetic test results in individuals at risk for Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Genetic testing: considerations for pediatric nephrologists

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

A systematic review of the impact of genetic counseling on risk perception accuracy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Anchoring-and-adjustment bias in communication of disease risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Meta-analysis of risk reduction estimates associated with risk-reducing salpingo-oophorectomy in BRCA1 or BRCA2 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Familial and hereditary renal cancer syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Presence of de novo mutations in autosomal dominant polycystic kidney disease patients without family history

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Molecular genetics of hereditary renal cancer: new genes and diagnostic and therapeutic opportunities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Interventions to improve risk communication in clinical genetics: systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

A systematic review of perceived risks, psychological and behavioral impacts of genetic testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Psychosocial and behavioral impact of genetic counseling and testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Risk reduction and health promotion behaviors following genetic testing for adult-onset disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Identification of the genes for kidney cancer: opportunity for disease-specific targeted therapeutics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Predictors and outcomes of contralateral prophylactic mastectomy among breast cancer survivors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Risk reduction behaviors and provider communication following genetic counseling and BRCA1 mutation testing in an African American kindred.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: systematic evidence review for the U.S. Preventive Services Task Force

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: recommendation statement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Psychological impact of genetic testing for cancer susceptibility: an update of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Psychosocial aspects of risk communication and mutation testing in familial breast-ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Effect of a computer-based decision aid on knowledge, perceptions, and intentions about genetic testing for breast cancer susceptibility: a randomized controlled trial

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Linking human genetics with molecular medicine: will hereditary renal cancer play a major role?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Assessment of genetic testing and related counseling services: current research and future directions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Randomised trial of a decision aid and its timing for women being tested for a BRCA1/2 mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Psychological impact of genetic counseling for familial cancer: a systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Hereditary kidney cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Effect of genetic cancer risk assessment on surgical decisions at breast cancer diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 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=2852315

4 July 2018

Psychological outcomes and risk perception after genetic testing and counselling in breast cancer: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Hereditary renal cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

BRCA1/2 genetic testing in the community setting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

What is the impact of genetic counselling in women at increased risk of developing hereditary breast cancer? A meta-analytic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Goals of genetic counseling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Psychological consequences of predictive genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a prospective follow-up study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

The impact of genetic counselling about breast cancer risk on women's risk perceptions and levels of distress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Family history of breast cancer: what do women understand and recall about their genetic risk?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

Controlled trial of pretest education approaches to enhance informed decision-making for BRCA1 gene testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

4 July 2018

The diversity of PKD1 alleles: implications for disease pathogenesis and genetic counseling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Interventions to improve patient education regarding multifactorial genetic conditions: a systematic review.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

A randomized trial of a breast/ovarian cancer genetic testing decision aid used as a communication aid during genetic counseling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Psychological distress and quality of life associated with genetic testing for breast cancer risk.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

ASCO/SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Risk-reducing surgery, screening and chemoprevention practices of BRCA1 and BRCA2 mutation carriers: a prospective cohort study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Patient responses to the disclosure of BRCA mutation tests in hereditary breast-ovarian cancer families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Colon cancer screening practices after genetic counseling and 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=2852315

30 October 2018

Utilization of breast cancer screening in a clinically based sample of women after BRCA1/2 testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

The use of audiotapes in consultations with women from high risk breast cancer families: a randomised trial

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Outcome of preventive surgery and screening for breast and ovarian cancer in BRCA mutation carriers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Comprehension of cancer risk one and 12 months after predictive genetic testing for hereditary non-polyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Genetic counseling forBRCA1/2: A randomized controlled trial of two strategies to facilitate the education and counseling process

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2852315

30 October 2018

Prophylactic surgery decisions and surveillance practices one year following BRCA1/2 testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Talking About Chance": The Presentation of Risk Information During Genetic Counseling for Breast and Ovarian Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral prophylactic oophorectomy and ovarian cancer screening following BRCA1/BRCA2 mutation testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic basis for kidney cancer: opportunity for disease-specific approaches to therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colon cancer screening practices following genetic testing for hereditary nonpolyposis colon cancer (HNPCC) mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pre-counseling education materials for BRCA testing: does tailoring make a difference?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening and preventive behaviors one year after predictive genetic testing for hereditary nonpolyposis colorectal carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling and testing for breast-ovarian cancer susceptibility: what do women want?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benefit finding in response to BRCA1/2 testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Randomized comparison of group versus individual genetic education and counseling for familial breast and/or ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced counseling for women undergoing BRCA1/2 testing: impact on subsequent decision making about risk reduction behaviors

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perceptions of cancer risks and predictors of colon and endometrial cancer screening in women undergoing genetic testing for Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of BRCA1/BRCA2 counseling and testing on newly diagnosed breast cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer risk counseling improves women’s functioning

1 reference

https://pubmed.ncbi.nlm.nih.gov/20347649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.SEMNEPHROL.2010.01.011

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

release_7ydl7o7jmrb6hhfji4uxhs3bga

1 reference

https://api.fatcat.wiki/v0/release/7ydl7o7jmrb6hhfji4uxhs3bga

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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