Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors (Q37963750)

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scientific article published on 02 December 2011

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English	Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors	scientific article published on 02 December 2011

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

author name string

Bronson D Riley

1

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Julie O Culver

2

1 reference

Europe PubMed Central

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26 August 2017

Cécile Skrzynia

3

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Leigha A Senter

4

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

June A Peters

5

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Josephine W Costalas

6

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Faith Callif-Daley

7

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Sherry C Grumet

8

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Katherine S Hunt

9

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Rebecca S Nagy

10

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Wendy C McKinnon

11

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Nancie M Petrucelli

12

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Robin L Bennett

13

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Angela M Trepanier

14

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

publication date

2 December 2011

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

Journal of Genetic Counseling

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Europe PubMed Central

PubMed publication ID

26 August 2017

21

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Europe PubMed Central

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26 August 2017

2

1 reference

Europe PubMed Central

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26 August 2017

151-161

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Europe PubMed Central

PubMed publication ID

26 August 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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The calculation of breast cancer risk for women with a first degree family history of ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

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Increased genetic counseling support improves communication of genetic information in families

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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Cowden syndrome: a critical review of the clinical literature

1 reference

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12 December 2020

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Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consent

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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Assessing women at high risk of breast cancer: a review of risk assessment models

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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Preimplantation genetic diagnosis for cancer predisposition syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

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Reconsidering the family history in primary care

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

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Accuracy of cancer family histories: comparison of two breast cancer syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

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Peer-support in coping with medical uncertainty: discussion of oophorectomy and hormone replacement therapy on a web-based message board

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

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Psychological Impact of Genetic Counseling for Familial Cancer: A Systematic Review and Meta-Analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer genetic testing: current and emerging issues

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethical Issues in Cancer Genetics: 1) Whose Information Is It?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer genetic counseling: communication and counselees' post-visit satisfaction, cognitions, anxiety, and needs fulfillment.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Projecting individualized probabilities of developing breast cancer for white females who are being examined annually

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathologic complete response rates in young women with BRCA1-positive breast cancers after neoadjuvant chemotherapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characteristics of health information gatherers, disseminators, and blockers within families at risk of hereditary cancer: implications for family health communication interventions.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

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Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

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/22134580

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/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of clinical practices among cancer genetic counselors

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Concise handbook of familial cancer susceptibility syndromes - second edition

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The BOADICEA model of genetic susceptibility to breast and ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stress and genetic testing for disease risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: a proof-of-concept trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

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/22134580

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/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Results of an intervention for individuals and families with BRCA mutations: a model for providing medical updates and psychosocial support following genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ASHG Statement* on Direct-to-Consumer Genetic Testing in the United States

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interventions to improve risk communication in clinical genetics: systematic review

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malignant transformation and new primary tumours after therapeutic radiation for benign disease: substantial risks in certain tumour prone syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

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Exploring hereditary cancer among dying cancer patients--a cross-sectional study of hereditary risk and perceived awareness of DNA testing and banking.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Randomized comparison of phone versus in-person BRCA1/2 predisposition genetic test result disclosure counseling.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of PENN II model to previous study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer genetic testing and assisted reproduction

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limited family structure and BRCA gene mutation status in single cases of breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anticipated versus actual emotional reactions to disclosure of results of genetic tests for cancer susceptibility: findings from p53 and BRCA1 testing programs

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

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/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer genetic risk assessment for individuals at risk of familial breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

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/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Standardized human pedigree nomenclature: update and assessment of the recommendations of the National Society of Genetic Counselors

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Medullary thyroid cancer: management guidelines of the American Thyroid Association

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychological responses to BRCA1 mutation testing: preliminary findings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective mismatch repair as a predictive marker for lack of efficacy of fluorouracil-based adjuvant therapy in colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Referral for cancer genetics consultation: a review and compilation of risk assessment criteria

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary cancer predisposition syndromes and preimplantation genetic diagnosis: where are we now?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

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/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NCCN clinical practice guidelines in oncology. Colorectal cancer screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disclosure of genetic information within families

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessing breast cancer risk and BRCA1/2 carrier probability.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling for breast cancer risk: general concepts, challenging themes and future directions

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Initial cancer genetic counseling consultation: Change in counselees' cognitions and anxiety, and association with addressing their needs and preferences

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethical issues in cancer genetics: I 1) whose information is it?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22134580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10897-011-9462-X

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

ResearchGate publication ID

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