(Q36824748)

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

scientific article published on 17 May 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

1 reference

Europe PubMed Central

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

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

1 reference

based on heuristic

inferred from title

author name string

Janice L Berliner

1

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Angela Musial Fay

2

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Practice Issues Subcommittee of the National Society of Genetic Counselors' Familial Cancer Risk Counseling Special Interest Group

3

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

publication date

17 May 2007

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Journal of Genetic Counseling

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

16

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

241-260

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

1 reference

https://api.crossref.org/works/10.1007%2FS10897-007-9090-7

21 January 2018

Cancer Incidence in BRCA1 mutation carriers

1 reference

https://api.crossref.org/works/10.1007%2FS10897-007-9090-7

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10897-007-9090-7

21 January 2018

Cancer Risk Estimates for BRCA1 Mutation Carriers Identified in a Risk Evaluation Program

1 reference

https://api.crossref.org/works/10.1007%2FS10897-007-9090-7

21 January 2018

Cost-effectiveness of screening BRCA1/2 mutation carriers with breast magnetic resonance imaging

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mortality after bilateral salpingo-oophorectomy in BRCA1 and BRCA2 mutation carriers: a prospective cohort study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accuracy of family cancer history in breast cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessing BRCA carrier probabilities in extended families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral prophylactic mastectomy reduces breast cancer risk in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of breast cancer risk prediction models in clinical practice

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 gene mutations: decision-making dilemmas concerning testing and management

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Banning genetic discrimination.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessing individual risk for breast cancer: risky business

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Update on the Manchester Scoring System for BRCA1 and BRCA2 testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

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/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing for cancer predisposition

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinical Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A low frequency of non-founder BRCA1 mutations in Ashkenazi Jewish breast-ovarian cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficacy of MRI and mammography for breast-cancer screening in women with a familial or genetic predisposition

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A breast cancer prediction model incorporating familial and personal risk factors.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation-Negative Hereditary Breast Cancer Families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-Uptake of Predictive Genetic Testing for BRCA1/2 among Relatives of Known Carriers: Attributes, Cancer Worry, and Barriers to Testing in a Multicenter Clinical Cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parity, Oral Contraceptives, and the Risk of Ovarian Cancer among Carriers and Noncarriers of aBRCA1orBRCA2Mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The accuracy of diagnoses as reported in families with cancer: a retrospective study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The accuracy of patient reports of a family history of cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychologic aspects of cancer genetic testing: a research update for clinicians

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling in a Navajo hereditary nonpolyposis colorectal cancer kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Code of ethical principles for genetics professionals: an explication

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling and clinical cancer genetics services

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk-reducing salpingo-oophorectomy in BRCA mutation carriers: role of serial sectioning in the detection of occult malignancy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the breast cancer susceptibility gene BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: an update

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers: an international case-control study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of the genetic counselor in familial cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cross-cultural issues in the disclosure of cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surveillance of BRCA1 and BRCA2 mutation carriers with magnetic resonance imaging, ultrasound, mammography, and clinical breast examination

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The risk of ovarian cancer after breast cancer in BRCA1 and BRCA2 carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary breast cancer in Jews

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing: psychological aspects and implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling for women with an intermediate family history of breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Time to reconsider subcutaneous mastectomy for breast-cancer prevention?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychological distress in women seeking genetic counseling for breast-ovarian cancer risk: the contributions of personality and appraisal

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mathematical modeling for breast cancer risk assessment. State of the art and role in medicine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A breast/ovarian cancer patient with germline mutations in both BRCA1 and BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of individualized breast cancer risk counseling: a randomized trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ovarian cancer risk counseling: a guide for the practitioner

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risks in BRCA2 mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Validation of family history data in cancer family registries

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 mutation carriers, oral contraceptive use, and breast cancer before age 50.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ovarian cancer screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risks in BRCA2 families: estimates for sites other than breast and ovary.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer surveillance in women with hereditary risk due to BRCA1 or BRCA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary cancers in children and ethical and psychosocial implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Understanding mathematical models for breast cancer risk assessment and counseling

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A review of the diagnosis and management of male breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study. Hereditary Breast Cancer Clinical Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of early-onset familial breast cancer to chromosome 17q21

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of Short-Term Hormone Replacement Therapy on Breast Cancer Risk Reduction After Bilateral Prophylactic Oophorectomy in BRCA1 and BRCA2 Mutation Carriers: The PROSE Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial ovarian cancer: a population-based case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The reliability of recollections of family history: implications for the medical provider.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychosocial Issues Associated with Genetic Testing for Breast and Ovarian Cancer Risk: An Integrative Review

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Laws restricting health insurers' use of genetic information: impact on genetic discrimination

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17508274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10897-007-9090-7

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 August 2017

ResearchGate publication ID

0 references

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