Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants. - Wikidata - awgldk - TriplyDB

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.

http://www.wikidata.org/entity/Q35576348

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Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project Privacy Attitudes among Early Adopters of Emerging Health Technologies Characterizing genetic variants for clinical action openSNP--a crowdsourced web resource for personal genomics Implications of Internet availability of genomic information for public health practice Advising patients about obtaining genomic profiles.Patient and provider attitudes toward genomic testing for prostate cancer susceptibility: a mixed method study.Genomic data in the electronic medical record: perspectives from a biobank community advisory board.Design and implementation of a randomized controlled trial of genomic counseling for patients with chronic disease.Genetics patients' perspectives on clinical genomic testing.Genetic counseling in direct-to-consumer exome sequencing: a case report.Gatekeepers or intermediaries? The role of clinicians in commercial genomic testing Direct-to-patient disclosure of results of mismatch repair screening for Lynch syndrome via electronic personal health record: a feasibility study.Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.Disclosure of genetic information and change in dietary intake: a randomized controlled trial.Attitudes towards Social Networking and Sharing Behaviors among Consumers of Direct-to-Consumer Personal Genomics.Current practice of public involvement activities in biomedical research and innovation: a systematic qualitative review.Consumers' intention to use health recommendation systems to receive personalized nutrition advice Understanding patient and provider perceptions and expectations of genomic medicine.Direct-to-consumer personalized genomic testing.Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology.Health care providers and direct-to-consumer access and advertising of genetic testing in the United States "It's not like judgment day": public understanding of and reactions to personalized genomic risk information An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practice Direct-to-consumer genomic testing: systematic review of the literature on user perspectives.Known unknowns: building an ethics of uncertainty into genomic medicine Interpretation of melanoma risk feedback in first-degree relatives of melanoma patients A randomized trial of genetic information for personalized nutrition Attitudes towards personal genomics among older Swiss adults: An exploratory study Public knowledge of and attitudes toward genetics and genetic testing.Translational Genomic Research: Protocol Development and Initial Outcomes following SNP Testing for Colon Cancer Risk.Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature.Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians Behavioral and psychosocial responses to genomic testing for colorectal cancer risk.Management of incidental findings in clinical genomic sequencing Primary care patients' views and decisions about, experience of and reactions to direct-to-consumer genetic testing: a longitudinal study.Direct-to-Consumer Genetic Testing and Personal Genomics Services: A Review of Recent Empirical Studies Opportunities for genomic clinical decision support interventions.Communicating genetic risk information for common disorders in the era of genomic medicine.

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Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.

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P2860

Direct to consumer genetic testing: Avoiding a culture war

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.

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

Disseminating innovations in health care.

Personal genomics and individual identities: motivations and moral imperatives of early users.

Future health applications of genomics: priorities for communication, behavioral, and social sciences research

Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes.

Participation in genetic testing research varies by social group.

Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.

Direct-to-consumer sales of genetic services on the Internet.

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