(Q36773744)

16 August 2017

Dealing with the unexpected: consumer responses to direct-access BRCA mutation testing (English)

1 reference

16 August 2017

7

Joanna L Mountain

1 reference

16 August 2017

Uta Francke

1

1 reference

16 August 2017

Cheri Dijamco

2

1 reference

16 August 2017

Amy K Kiefer

3

1 reference

16 August 2017

Nicholas Eriksson

4

1 reference

16 August 2017

Bianca Moiseff

5

1 reference

16 August 2017

Joyce Y Tung

6

1 reference

16 August 2017

12 February 2013

1 reference

16 August 2017

1 reference

16 August 2017

1

1 reference

16 August 2017

e8

1 reference

An informatics approach to analyzing the incidentalome

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Exploring concordance and discordance for return of incidental findings from clinical sequencing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Direct to consumer genetic testing: a systematic review of position statements, policies and recommendations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

A family experience of personal genomics.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Long-term outcomes of BRCA1/BRCA2 testing: risk reduction and surveillance

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Case report: BRCA in the Ashkenazi population: are current testing guidelines too exclusive?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Effect of direct-to-consumer genomewide profiling to assess disease risk

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

BRCA1 and BRCA2 germline mutation analysis among Indian women from south India: identification of four novel mutations and high-frequency occurrence of 185delAG mutation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Disclosure of APOE genotype for risk of Alzheimer's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Emotional distress following genetic testing for hereditary breast and ovarian cancer: a meta-analytic review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Clinical practice. Management of an inherited predisposition to breast cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Meta-analysis of BRCA1 and BRCA2 penetrance

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Identification of germline 185delAG BRCA1 mutations in non-Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Prevalence of BRCA1 and BRCA2 Jewish mutations in Spanish breast cancer patients.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Risk-reducing mastectomy and salpingo-oophorectomy in unaffected BRCA mutation carriers: uptake and timing

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Predictive testing for BRCA1 and 2 mutations: a male contribution.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Screening for founder mutations in BRCA1 and BRCA2 in unselected Jewish women

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

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

20 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.7717%2FPEERJ.8

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3628894

Risks of presymptomatic direct-to-consumer genetic testing

20 October 2018

1 reference

12 December 2020

Swiss primary care physicians' knowledge, attitudes and perception towards genetic testing for hereditary breast cancer

1 reference

12 December 2020

Long-term follow-up of Jewish women with a BRCA1 and BRCA2 mutation who underwent population genetic screening

1 reference

12 December 2020

Psychological distress with direct-to-consumer genetic testing: a case report of an unexpected BRCA positive test result

1 reference

12 December 2020

Identifiers

DOI

10.7717/PEERJ.8

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

23638402

1 reference