Public experiences, knowledge and expectations about medical genetics and the use of genetic information.
about
Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general publicThe implications of genetic susceptibility for the prevention of colorectal cancer: a qualitative study of older adults' understanding.Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectivesA novel, privacy-preserving cryptographic approach for sharing sequencing data.Genetic Knowledge Among Participants in the Coriell Personalized Medicine CollaborativeGenePING: secure, scalable management of personal genomic data.Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives.Cultural beliefs on disease causation in the Philippines: challenge and implications in genetic counseling.Consumers' intention to use health recommendation systems to receive personalized nutrition adviceSubjects' expectations in neuroimaging research.Age differences in genetic knowledge, health literacy and causal beliefs for health conditionsWhat's at stake? Genetic information from the perspective of people with epilepsy and their family members.Veterans' experience in using the online Surgeon General's family health history tool.Breast cancer genetic counselling referrals: how comparable are the findings between the UK and the Netherlands?Experiences and attitudes of residents regarding a community-based genome cohort study in Japan: a population-based, cross-sectional study.Patients' understanding of and responses to multiplex genetic susceptibility test resultsRevealing barriers and facilitators to use a new genetic test: comparison of three user involvement methods.Effects of informed consent for individual genome sequencing on relevant knowledge.How to foster citizens' statistical reasoning: implications for genetic counseling.Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestryPublic attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010Educating the general public about multifactorial genetic disease: applying a theory-based framework to understand current public knowledge.Knowledge of and interest in genetic results among Parkinson disease patients and caregivers.Consulting the community: public expectations and attitudes about genetics research.It's complicated - Factors predicting decisional conflict in prenatal diagnostic testing.Community engagement with genetics: public perceptions and expectations about genetics research.Association of education & lifestyle factors with the perception of genetic knowledge on the development of lung cancer.Measuring genetic knowledge: a brief survey instrument for adolescents and adults.Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society.Modern Advances in Genetic Testing: Ethical Challenges and Training Implications for Current and Future Psychologists.Incidental findings from clinical genome-wide sequencing: a review.Tailored chemotherapy based on tumour gene expression analysis: breast cancer patients' misinterpretations and positive attitudes.Long-term experiences with genetic consultation in people with hereditary breast and ovarian cancer.Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.Applying a theory-based framework to understand public knowledge of genetic risk factors: a case for the distinction between how-to knowledge and principles knowledge.The public's attitudes towards the use of genetic information for medical purposes and its related factors in Japan.Knowledge, Attitudes, and Practice Regarding Genetic Testing and Genetic Counselors in Jordan: A Population-Based Survey.Employees are ambivalent about health checks in the occupational setting.Community genetics: 1998-2009…and beyond.Research 2.0: social networking and direct-to-consumer (DTC) genomics.
P2860
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P2860
Public experiences, knowledge and expectations about medical genetics and the use of genetic information.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Public experiences, knowledge ...... he use of genetic information.
@en
type
label
Public experiences, knowledge ...... he use of genetic information.
@en
prefLabel
Public experiences, knowledge ...... he use of genetic information.
@en
P2860
P50
P356
P1476
Public experiences, knowledge ...... he use of genetic information.
@en
P2093
Danielle R M Timmermans
Gerrit van der Wal
P2860
P356
10.1159/000080302
P577
2004-01-01T00:00:00Z