scholarly article | Q13442814 |
P356 | DOI | 10.1038/GIM.2015.135 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/gim.2015.135 |
P698 | PubMed publication ID | 26540155 |
P50 | author | Pavel Hamet | Q3372940 |
William David Foulkes | Q37829195 | ||
Jacques Simard | Q64516110 | ||
P2093 | author name string | Michel Dorval | |
Jocelyne Chiquette | |||
Sylvie Pelletier | |||
Nora Wong | |||
Zaki El Haffaf | |||
P2860 | cites work | Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies | Q24531993 |
Efficacy of statins for primary prevention in people at low cardiovascular risk: a meta-analysis | Q24628361 | ||
Recommendations on screening for breast cancer in average-risk women aged 40-74 years | Q24633913 | ||
Preventive health care, 2001 update: screening mammography among women aged 40-49 years at average risk of breast cancer | Q28203101 | ||
Screening for breast cancer: U.S. Preventive Services Task Force recommendation statement | Q28265041 | ||
BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA-negative experience | Q33576901 | ||
Patients' anxiety and expectations: how they influence family physicians' decisions to order cancer screening tests | Q34682487 | ||
Combined associations of genetic and environmental risk factors: implications for prevention of breast cancer | Q34736112 | ||
Breast and ovarian cancer screening of non-carriers from BRCA1/2 mutation-positive families: 2-year follow-up of cohorts from France and Quebec | Q34873841 | ||
Breast cancer risk for noncarriers of family-specific BRCA1 and BRCA2 mutations: findings from the Breast Cancer Family Registry | Q35609710 | ||
Falling through the cracks. Women's experiences of ineligibility for genetic testing for risk of breast cancer | Q36282425 | ||
Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
Predictive genetic testing for BRCA1/2 in a UK clinical cohort: three-year follow-up | Q36610024 | ||
Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National Society of Genetic Counselors | Q36824748 | ||
Experience of BRCA1/2 mutation-negative young women from families with hereditary breast and ovarian cancer: a qualitative study | Q37312028 | ||
From candidate gene studies to GWAS and post-GWAS analyses in breast cancer | Q38366358 | ||
Comparison of the screening practices of unaffected noncarriers under 40 and between 40 and 49 in BRCA1/2 families | Q39480009 | ||
Making decisions about cancer screening when the guidelines are unclear or conflicting | Q39576818 | ||
Rigour and qualitative research | Q40445898 | ||
Qualitative research: standards, challenges, and guidelines | Q42657344 | ||
"I have always believed I was at high risk..." The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments. | Q44436660 | ||
Cancer risk comparative perception and overscreening behaviours of non-carriers from BRCA1/2 families | Q44568691 | ||
Breast cancer risks in individuals testing negative for a known family mutation in BRCA1 or BRCA2. | Q46520947 | ||
[Identification and management of hereditary predisposition to cancer of the breast and the ovary (update 2004)]. | Q49316774 | ||
Cancer risk management practices of noncarriers within BRCA1/2 mutation positive families in the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer. | Q51726517 | ||
A gift or a yoke? Women's and men's responses to genetic risk information from BRCA1 and BRCA2 testing. | Q52574933 | ||
Breast Cancer Risk for Noncarriers of Family-SpecificBRCA1andBRCA2Mutations: More Trouble With Phenocopies | Q57266555 | ||
The effect of experiential knowledge on construction of risk perception in hereditary breast/ovarian cancer | Q81571149 | ||
Phenocopy breast cancer rates in Israeli BRCA1 BRCA2 mutation carrier families: is the risk increased in non-carriers? | Q82660651 | ||
Prospective study of breast cancer risk for mutation negative women from BRCA1 or BRCA2 mutation positive families | Q84785212 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | ovarian cancer | Q172341 |
P304 | page(s) | 627-34 | |
P577 | publication date | 2016-06-01 | |
P1433 | published in | Genetics in Medicine | Q15765508 |
P1476 | title | Clinical follow-up and breast and ovarian cancer screening of true BRCA1/2 noncarriers: a qualitative investigation | |
P478 | volume | 18 |
Search more.