Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers. - Wikidata - awgldk - TriplyDB

Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.

Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.

http://www.wikidata.org/entity/Q34379754

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Users' motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review Field of genes: an investigation of sports-related genetic testing The effect of communicating the genetic risk of cardiometabolic disorders on motivation and actual engagement in preventative lifestyle modification and clinical outcome: a systematic review and meta-analysis of randomised controlled trials.All your data (effectively) belong to us: data practices among direct-to-consumer genetic testing firms.Health Orientation, Knowledge, and Attitudes toward Genetic Testing and Personalized Genomic Services: Preliminary Data from an Italian Sample.Self-reported race and ethnicity of US biobank participants compared to the US Census Tilting at windmills no longer: a data-driven discussion of DTC DNA ancestry tests.Consumers' use of web-based information and their decisions about multiplex genetic susceptibility testing Attitudes towards Social Networking and Sharing Behaviors among Consumers of Direct-to-Consumer Personal Genomics.Preconceptional genetic carrier testing and the commercial offer directly-to-consumers Direct-to-consumer personalized genomic testing.Information-seeking and sharing behavior following genomic testing for diabetes risk.Health care providers and direct-to-consumer access and advertising of genetic testing in the United States Informed choice in direct-to-consumer genetic testing (DTCGT) websites: a content analysis of benefits, risks, and limitations."It's not like judgment day": public understanding of and reactions to personalized genomic risk information Genetics blogs as a public health tool: assessing credibility and influence Consumers report lower confidence in their genetics knowledge following direct-to-consumer personal genomic testing Patients' understanding of and responses to multiplex genetic susceptibility test results A randomized trial of genetic information for personalized nutrition Update on Direct-to-Consumer Marketing in Oncology.State of play in direct-to-consumer genetic testing for lifestyle-related diseases: market, marketing content, user experiences and regulation.Patient knowledge and information-seeking about personalized cancer therapy.Marketing of personalized cancer care on the web: an analysis of Internet websites Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature.The impact of risk information exposure on women's beliefs about direct-to-consumer genetic testing for BRCA mutations.Communicating genetic risk information for common disorders in the era of genomic medicine.Neither as harmful as feared by critics nor as empowering as promised by providers: risk information offered direct to consumer by personal genomics companies.Characteristics of genetics-related news content in Black weekly newspapers.Direct to consumer genetic testing: a systematic review of position statements, policies and recommendations.Current landscape of direct-to-consumer genetic testing and its role in ophthalmology: a review.Third party interpretation of raw genetic data: an ethical exploration.A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents.Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.A tiered-layered-staged model for informed consent in personal genome testing.Pre- and post-testing counseling considerations for the provision of expanded carrier screening: exploration of European geneticists' views Public awareness and use of direct-to-consumer personal genomic tests from four state population-based surveys, and implications for clinical and public health practice.Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing.Effect of direct-to-consumer genetic tests on health behaviour and anxiety: a survey of consumers and potential consumers.Direct-to-consumer advertising of predictive genetic tests: a health belief model based examination of consumer response.

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Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.

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2010年の論文

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Genetics in Medicine

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Christina R Lachance

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Kimberly A Kaphingst

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A vision for the future of genomics research

Letting the genome out of the bottle--will we get our wish?

Developing the blueprint for a genetic testing registry

General performance on a numeracy scale among highly educated samples.

Direct to consumer genetic testing: Avoiding a culture war

Risk information exposure and direct-to-consumer genetic testing for BRCA mutations among women with a personal or family history of breast or ovarian cancer.

Limitations of direct-to-consumer advertising for clinical genetic testing.

Internet usage by low-literacy adults seeking health information: an observational analysis

Smoking cessation treatment on the Internet: content, quality, and usability.

Genetic testing: practical, ethical, and counseling considerations.

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