| scholarly article | Q13442814 |
| P50 | author | Siang Ing Lee | Q85250877 |
| Brittany Dutton | Q91811500 | ||
| Nadeem Qureshi | Q40731118 | ||
| P2093 | author name string | Mitesh Patel | |
| Stephen Weng | |||
| Jocelyn Luveta | |||
| P2860 | cites work | A cohort study of cancer risk in relation to family histories of cancer in the Utah population database | Q81547804 |
| The genomic medicine model: an integrated approach to implementation of family health history in primary care | Q88695399 | ||
| Cancer genetic risk assessment for individuals at risk of familial breast cancer | Q24203650 | ||
| Cancer risk assessment tools in primary care: a systematic review of randomized controlled trials | Q26786902 | ||
| The Cochrane Collaboration's tool for assessing risk of bias in randomised trials | Q27860509 | ||
| Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation | Q29615706 | ||
| Selective oestrogen receptor modulators in prevention of breast cancer: an updated meta-analysis of individual participant data | Q30620889 | ||
| Family history and perceptions about risk and prevention for chronic diseases in primary care: a report from the family healthware impact trial | Q33679444 | ||
| Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system | Q34046666 | ||
| Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2. | Q34103057 | ||
| Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality | Q34135443 | ||
| Effect of preventive messages tailored to family history on health behaviors: the Family Healthware Impact Trial | Q34496337 | ||
| Patient and primary care provider experience using a family health history collection, risk stratification, and clinical decision support tool: a type 2 hybrid controlled implementation-effectiveness trial | Q34894629 | ||
| Improving the referral process for familial breast cancer genetic counselling: findings of three randomised controlled trials of two interventions | Q36031666 | ||
| Clinical utility of family history for cancer screening and referral in primary care: a report from the Family Healthware Impact Trial | Q36182632 | ||
| Family history assessment: impact on disease risk perceptions | Q36250488 | ||
| The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary care | Q36611002 | ||
| ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions | Q37335426 | ||
| The current state of cancer family history collection tools in primary care: a systematic review | Q37517079 | ||
| Components of family history associated with women's disease perceptions for cancer: a report from the Family Healthware™ Impact Trial | Q37590233 | ||
| Online self-test identifies women at high familial breast cancer risk in population-based breast cancer screening without inducing anxiety or distress. | Q38835427 | ||
| Evaluation of mammographic surveillance services in women aged 40-49 years with a moderate family history of breast cancer: a single-arm cohort study. | Q40097974 | ||
| Clinical utility of a Web-enabled risk-assessment and clinical decision support program | Q40874216 | ||
| Familial risk for common diseases in primary care: the Family Healthware Impact Trial | Q43701268 | ||
| Population prevalence of familial cancer and common hereditary cancer syndromes. The 2005 California Health Interview Survey | Q44181640 | ||
| Implementing family health history risk stratification in primary care: impact of guideline criteria on populations and resource demand | Q46705869 | ||
| Risk-reducing mastectomy for the prevention of primary breast cancer. | Q52604887 | ||
| Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: Recommendation Statement. | Q53776550 | ||
| Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer | Q57567891 | ||
| Cluster randomized trial of a multifaceted primary care decision-support intervention for inherited breast cancer risk | Q58377122 | ||
| What characterizes cancer family history collection tools? A critical literature review | Q58783269 | ||
| Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening† | Q59273721 | ||
| How common is familial cancer? | Q81097413 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 73-83 | |
| P577 | publication date | 2019-05-06 | |
| P1433 | published in | Journal of Community Genetics | Q15816656 |
| P1476 | title | Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review | |
| P478 | volume | 11 |
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