scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1106082560 |
P356 | DOI | 10.1007/S12687-018-0378-0 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1007/s12687-018-0378-0 |
P932 | PMC publication ID | 6435778 |
P698 | PubMed publication ID | 30097836 |
P50 | author | Laura E Forrest | Q90024300 |
P2093 | author name string | Mary-Anne Young | |
Nina Hallowell | |||
Sarah Dilys Sawyer | |||
Paul Andrew James | |||
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 |
Large-scale genotyping identifies 41 new loci associated with breast cancer risk | Q29416989 | ||
Re-conceptualizing risk in genetic counseling: implications for clinical practice | Q30385147 | ||
Alcohol, tobacco and breast cancer--collaborative reanalysis of individual data from 53 epidemiological studies, including 58,515 women with breast cancer and 95,067 women without the disease | Q30747351 | ||
Public preferences for communicating personal genomic risk information: a focus group study | Q30830961 | ||
Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study | Q33916899 | ||
Using icon arrays to communicate medical risks: overcoming low numeracy | Q34963595 | ||
Interest in genetic testing for modest changes in breast cancer risk: implications for SNP testing. | Q35016127 | ||
Interest in genomic SNP testing for prostate cancer risk: a pilot survey. | Q35403712 | ||
Risk communication strategies: state of the art and effectiveness in the context of cancer genetic services | Q35545038 | ||
8. Cancers attributable to overweight and obesity in the UK in 2010. | Q35654721 | ||
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer | Q35996692 | ||
Simple tools for understanding risks: from innumeracy to insight | Q36037510 | ||
The contributions of breast density and common genetic variation to breast cancer risk | Q36137764 | ||
Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
"Is it really worth it to get tested?": primary care patients' impressions of predictive SNP testing for colon cancer | Q36595655 | ||
Translational Genomic Research: Protocol Development and Initial Outcomes following SNP Testing for Colon Cancer Risk | Q36738056 | ||
Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab | Q37410693 | ||
Incorporating genomics into breast and prostate cancer screening: assessing the implications | Q37614763 | ||
Common breast cancer risk variants in the post-COGS era: a comprehensive review | Q37690575 | ||
The psychological impact of undergoing genetic-risk profiling in men with a family history of prostate cancer | Q39018270 | ||
"It's all very well reading the letters in the genome, but it's a long way to being able to write": Men's interpretations of undergoing genetic profiling to determine future risk of prostate cancer | Q39167311 | ||
Psychiatric genetic counselling for parents of individuals affected with psychotic disorders: a pilot study | Q40097715 | ||
Family stories and the use of heuristics: women from suspected hereditary breast and ovarian cancer (HBOC) families. | Q40552820 | ||
Breast cancer risk prediction using a clinical risk model and polygenic risk score | Q40605693 | ||
Women's preferences and consultants' communication of risk in consultations about familial breast cancer: impact on patient outcomes | Q43074138 | ||
Personal theories of inheritance, coping strategies, risk perception and engagement in hereditary non-polyposis colon cancer families offered genetic testing | Q47381625 | ||
Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks. | Q47822347 | ||
'A low risk is still a risk': exploring women's attitudes towards genetic testing for breast cancer susceptibility in order to target disease prevention | Q48233913 | ||
The effect of experiential knowledge on construction of risk perception in hereditary breast/ovarian cancer | Q81571149 | ||
A role for common genomic variants in the assessment of familial breast cancer | Q85312916 | ||
P433 | issue | 2 | |
P304 | page(s) | 197-206 | |
P577 | publication date | 2018-08-10 | |
P1433 | published in | Journal of Community Genetics | Q15816656 |
P1476 | title | High-risk women's risk perception after receiving personalized polygenic breast cancer risk information | |
P478 | volume | 10 |
Q89746441 | Clinical applications of polygenic breast cancer risk: a critical review and perspectives of an emerging field |
Q90814312 | Genetic 3'UTR variations and clinical factors significantly contribute to survival prediction and clinical response in breast cancer patients |
Q90460444 | Illustrating Cancer Risk: Patient Risk Communication Preferences and Interest regarding a Novel BRCA1/2 Genetic Risk Modifier Test |
Search more.