Public knowledge of and attitudes toward genetics and genetic testing. - Wikidata - awgldk - TriplyDB

Public knowledge of and attitudes toward genetics and genetic testing.

Public knowledge of and attitudes toward genetics and genetic testing.

http://www.wikidata.org/entity/Q36720757

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Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative Genomic data in the electronic medical record: perspectives from a biobank community advisory board.Impact of delivery models on understanding genomic risk for type 2 diabetes Public trust in genomic risk assessment for type 2 diabetes mellitus.Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review.Genetic information, non-discrimination, and privacy protections in genetic counseling practice.Genetics and primary care: where are we headed?Is there a moral obligation to conceive children under the best possible conditions? A preliminary framework for identifying the preconception responsibilities of potential parents.The value of personalizing medicine: medical oncologists' views on gene expression profiling in breast cancer treatment Parent and public interest in whole-genome sequencing Information-seeking and sharing behavior following genomic testing for diabetes risk.Genetic Information-Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes.The Many Facets of Genetic Literacy: Assessing the Scalability of Multiple Measures for Broad Use in Survey Research.Experiences and attitudes of residents regarding a community-based genome cohort study in Japan: a population-based, cross-sectional study.Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders Patient knowledge and information-seeking about personalized cancer therapy.Training the Future Leaders in Personalized Medicine Ethical challenges in preclinical Alzheimer's disease observational studies and trials: Results of the Barcelona summit.How Well Do Customers of Direct-to-Consumer Personal Genomic Testing Services Comprehend Genetic Test Results? Findings from the Impact of Personal Genomics Study My Cancer Genome: Evaluating an Educational Model to Introduce Patients and Caregivers to Precision Medicine Information.Health coaching and genomics-potential avenues to elicit behavior change in those at risk for chronic disease: protocol for personalized medicine effectiveness study in air force primary care.Measuring genetic knowledge: a brief survey instrument for adolescents and adults.Promoting healthy dietary behaviour through personalised nutrition: technology push or technology pull?Genomic-based tools for the risk assessment, management, and prevention of type 2 diabetes.Genes, cells, and biobanks: Yes, there's still a consent problem.A Qualitative Look into Israeli Genetic Experts' Insights Regarding Culturally Competent Genetic Counseling and Recommendations for Its Enhancement.Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.Population-based biobank participants' preferences for receiving genetic test results.The Moral Reasoning of Genetic Dilemmas Amongst Jewish Israeli Undergraduate Students with Different Religious Affiliations and Scientific Backgrounds.Influence of family history on the willingness of outpatients to undergo genetic testing for salt-sensitive hypertension: a cross-sectional study.Public Views on Genetics and Genetic Testing: A Survey of the General Public in Belgium.HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD).The price of whole-genome sequencing may be decreasing, but who will be sequenced?Motivation, Perception, and Treatment Beliefs in the Myocardial Infarction Genes (MI-GENES) Randomized Clinical Trial.A Qualitative Study of Anticipated Decision Making around Type 2 Diabetes Genetic Testing: the Role of Scientifically Concordant and Discordant Expectations."Where Does it Come from?" Experiences Among Survivors and Parents of Children with Retinoblastoma in Kenya.Prospects for using risk scores in polygenic medicine.Parents' Understanding of Genetics and Heritability.Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach.

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P2860

Public knowledge of and attitudes toward genetics and genetic testing.

http://www.wikidata.org/entity/Q36720757

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年论文

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2013年论文

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name

Public knowledge of and attitudes toward genetics and genetic testing.

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Public knowledge of and attitudes toward genetics and genetic testing.

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type

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Public knowledge of and attitudes toward genetics and genetic testing.

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Public knowledge of and attitudes toward genetics and genetic testing.

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Public knowledge of and attitudes toward genetics and genetic testing.

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Public knowledge of and attitudes toward genetics and genetic testing.

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Genetic Testing and Molecular Biomarkers

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Public knowledge of and attitudes toward genetics and genetic testing.

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Geoffrey S Ginsburg

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Huntington F Willard

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Jennifer Sullivan

http://www.w3.org/2001/XMLSchema#string

Laura Svetkey

http://www.w3.org/2001/XMLSchema#string

Rachel Mills

http://www.w3.org/2001/XMLSchema#string

Susanne B Haga

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William T Barry

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P2860

Web-based, participant-driven studies yield novel genetic associations for common traits

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease

Trends in U.S. Attitudes Toward Genetic Testing, 1990-2004

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

The test of functional health literacy in adults: a new instrument for measuring patients' literacy skills

Using lifetime risk estimates in personal genomic profiles: estimation of uncertainty

Efficient replication of over 180 genetic associations with self-reported medical data

Worlds apart? The reception of genetically modified foods in Europe and the U.S.

Communicating genetic and genomic information: health literacy and numeracy considerations

Effect of direct-to-consumer genomewide profiling to assess disease risk.

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10.1089/GTMB.2012.0350

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4

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17

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23406207

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3609633

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