scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1090746107 |
P356 | DOI | 10.1186/S12885-017-3485-0 |
P932 | PMC publication ID | 5516374 |
P698 | PubMed publication ID | 28720130 |
P50 | author | Bettina Meiser | Q60641709 |
Kristine Barlow-Stewart | Q69373743 | ||
P2093 | author name string | Paul James | |
Gillian Mitchell | |||
Tony Roscioli | |||
Jane Halliday | |||
Mary-Anne Young | |||
Rajneesh Kaur | |||
Tatiane Yanes | |||
P2860 | cites work | Large-scale genotyping identifies 41 new loci associated with breast cancer risk | Q29416989 |
Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease | Q30665466 | ||
Emotional distress following genetic testing for hereditary breast and ovarian cancer: a meta-analytic review | Q33594181 | ||
The validity of the Hospital Anxiety and Depression Scale. An updated literature review | Q34113060 | ||
Genome-wide association study identifies five new breast cancer susceptibility loci | Q34114293 | ||
Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality | Q34135443 | ||
Interpretation of changes in health-related quality of life: the remarkable universality of half a standard deviation | Q34193483 | ||
Interest in genetic testing for modest changes in breast cancer risk: implications for SNP testing. | Q35016127 | ||
Beliefs about weight and breast cancer: an interview study with high risk women following a 12 month weight loss intervention | Q35041396 | ||
Interest in genomic SNP testing for prostate cancer risk: a pilot survey. | Q35403712 | ||
Making hard choices easier: a prospective, multicentre study to assess the efficacy of a fertility-related decision aid in young women with early-stage breast cancer | Q35832375 | ||
The genetic epidemiology of breast cancer genes | Q35959353 | ||
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer | Q35996692 | ||
Psychological impact of genetic testing for cancer susceptibility: an update of the literature | Q36153016 | ||
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 | ||
Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry | Q36619329 | ||
Translational Genomic Research: Protocol Development and Initial Outcomes following SNP Testing for Colon Cancer Risk | Q36738056 | ||
Risk reduction and health promotion behaviors following genetic testing for adult-onset disorders | Q36879101 | ||
Behavioral and psychosocial responses to genomic testing for colorectal cancer risk | Q37060585 | ||
Meta-analysis of risk reduction estimates associated with risk-reducing salpingo-oophorectomy in BRCA1 or BRCA2 mutation carriers | Q37090813 | ||
Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families | Q37131918 | ||
Genetic counseling as a tool for type 2 diabetes prevention: a genetic counseling framework for common polygenetic disorders | Q37312886 | ||
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 | ||
Interest and informational preferences regarding genomic testing for modest increases in colorectal cancer risk | Q37711233 | ||
Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors | Q37963750 | ||
Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning? | Q38131236 | ||
Impact of Event Scale: A Measure of Subjective Stress | Q39513124 | ||
Factors influencing intention to undergo whole genome screening in future healthcare: a single-blind parallel-group randomised trial. | Q39560593 | ||
Psychiatric genetic counselling for parents of individuals affected with psychotic disorders: a pilot study | Q40097715 | ||
Personalized Medicine Through SNP Testing for Breast Cancer Risk: Clinical Implementation | Q46621012 | ||
Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families | Q46735021 | ||
BRCA1 testing with definitive results: a prospective study of psychological distress in a large clinic-based sample | Q47343483 | ||
Application of the protection motivation theory to genetic testing for breast cancer risk. | Q48614853 | ||
Predictors of breast cancer screening behavior in women with a strong family history of the disease. | Q50699640 | ||
Validation of a decision regret scale. | Q51019738 | ||
Psychological impact of genetic testing in women from high-risk breast cancer families. | Q51037248 | ||
Psychometric properties of the Impact of Event Scale amongst women at increased risk for hereditary breast cancer. | Q51059520 | ||
A brief assessment of concerns associated with genetic testing for cancer: the Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire. | Q54268435 | ||
Genetic Testing for Women Previously Diagnosed with Breast/Ovarian Cancer: Examining the Impact of BRCA1 and BRCA2 Mutation Searching | Q57694666 | ||
The List of Threatening Experiences: the reliability and validity of a brief life events questionnaire | Q68918765 | ||
Impact of BRCA1/2 testing and disclosure of a positive test result on women affected and unaffected with breast or ovarian cancer | Q75306808 | ||
Impact of BRCA1/BRCA2 mutation testing on psychologic distress in a clinic-based sample | Q77476124 | ||
American society of clinical oncology clinical practice guideline update on the use of pharmacologic interventions including tamoxifen, raloxifene, and aromatase inhibition for breast cancer risk reduction | Q83917287 | ||
A role for common genomic variants in the assessment of familial breast cancer | Q85312916 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 491 | |
P577 | publication date | 2017-07-18 | |
P1433 | published in | BMC Cancer | Q326300 |
P1476 | title | Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study | |
P478 | volume | 17 |
Q64934338 | High-risk women's risk perception after receiving personalized polygenic breast cancer risk information. | cites work | P2860 |
Search more.