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Towards a comprehensive structural variation map of an individual human genomeGenetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disordersPersonality and longevity: knowns, unknowns, and implications for public health and personalized medicineClinical utility of sequence-based genotype compared with that derivable from genotyping arraysMultiplex meta-analysis of RNA expression to identify genes with variants associated with immune dysfunctionInternet-Based Direct-to-Consumer Genetic Testing: A Systematic ReviewTeaching residents genomic pathology: a novel approach for new technologyTranslational bioinformatics: linking the molecular world to the clinical worldIdentifiability in biobanks: models, measures, and mitigation strategiesUsing lifetime risk estimates in personal genomic profiles: estimation of uncertaintyCrowdsourced direct-to-consumer genomic analysis of a family quartetBioinformatics for personal genome interpretationImplications of Internet availability of genomic information for public health practiceHow do SNP ascertainment schemes and population demographics affect inferences about population history?Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utilityAdvising patients about obtaining genomic profiles.Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized MedicineEnhancing systems medicine beyond genotype data by dynamic patient signatures: having information and using it tooGerman Ethics Council on genetic diagnostics: trend setting?A survey of UK public interest in internet-based personal genome testing.Comparison of commercial genetic-testing services in Korea with 23andMe service.Evaluating the accuracy of AIM panels at quantifying genome ancestryLikelihood ratios for genome medicine.Identifying subtypes of patients with neovascular age-related macular degeneration by genotypic and cardiovascular risk characteristics.Genetic testing integration panels (GTIPs): a novel approach for considering integration of direct-to-consumer and other new genetic tests into patient care.Practical considerations to guide development of access controls and decision support for genetic information in electronic medical recordsEthical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practiceMisuse (and abuse?) of the Concept of Empowerment.The Case of Online Offer of Predictive Direct-to-consumer Genetic TestsThe emergence of translational epidemiology: from scientific discovery to population health impact.Estimating and disclosing the risk of developing Alzheimer's disease: challenges, controversies and future directionsImplementation and utilization of genetic testing in personalized medicine.Effect of direct-to-consumer genomewide profiling to assess disease risk.Examining moderation analyses in propensity score methods: application to depression and substance use.Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.Genetic tests: between risks and opportunities. The case of neurodegenerative diseases.Health-care referrals from direct-to-consumer genetic testingAttitudes towards Social Networking and Sharing Behaviors among Consumers of Direct-to-Consumer Personal Genomics.Nutrigenetics and nutrigenomics: viewpoints on the current status and applications in nutrition research and practice.Genomics for disease treatment and prevention.K(ATP) channel-dependent metaboproteome decoded: systems approaches to heart failure prediction, diagnosis, and therapy.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
An agenda for personalized medicine.
@en
An agenda for personalized medicine.
@nl
type
label
An agenda for personalized medicine.
@en
An agenda for personalized medicine.
@nl
prefLabel
An agenda for personalized medicine.
@en
An agenda for personalized medicine.
@nl
P2093
P356
P1433
P1476
An agenda for personalized medicine.
@en
P2093
Pauline C Ng
Samuel Levy
Sarah S Murray
P2888
P304
P356
10.1038/461724A
P407
P577
2009-10-01T00:00:00Z
P5875
P6179
1032295844