标题
From the patient to the population: Use of genomics for population screening
作者
关键词
-
出版物
Frontiers in Genetics
Volume 13, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2022-10-24
DOI
10.3389/fgene.2022.893832
参考文献
相关参考文献
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- A comparison of the detection of BRCA mutation carriers through the provision of Jewish population-based genetic testing compared with clinic-based genetic testing
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- Modeling Good Research Practices—Overview
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- (2011) André R. Maddison et al. CANCER CAUSES & CONTROL
- Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations
- (2011) A. Moran et al. Familial Cancer
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- (2011) L. Nherera et al. HEART
- Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome
- (2011) Valérie Bonadona JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
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- Critical Race Theory, Race Equity, and Public Health: Toward Antiracism Praxis
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- Health Benefits and Cost-Effectiveness of Primary Genetic Screening for Lynch Syndrome in the General Population
- (2010) T. A. Dinh et al. Cancer Prevention Research
- Patient satisfaction and cancer-related distress among unselected Jewish women undergoing genetic testing for BRCA1 and BRCA2
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- The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) initiative: methods of the EGAPP Working Group
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- Screening for Founder Mutations in BRCA1 and BRCA2 in Unselected Jewish Women
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- Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers
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- Sensitivity and specificity of multimodal and ultrasound screening for ovarian cancer, and stage distribution of detected cancers: results of the prevalence screen of the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS)
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- Hereditary ovarian carcinoma: Heterogeneity, molecular genetics, pathology, and management
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- Guiding Policy Decisions for Genetic Screening: Developing a Systematic and Transparent Approach
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- Revisting wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years
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- The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations
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- Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer
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