about
Genetic 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 disordersMeasuring paternal discrepancy and its public health consequencesFamily history of heart disease and cardiovascular disease risk-reducing behaviorsPatients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophiliaThe path from genome-based research to population health: development of an international public health genomics networkGenetics through a primary care lens.A research agenda for assessing the potential contribution of genomic medicine to tobacco control.Web-based self-assessment health tools: who are the users and what is the impact of missing input information?Bupropion efficacy for smoking cessation is influenced by the DRD2 Taq1A polymorphism: analysis of pooled data from two clinical trials.How should risk be communicated to children: a cross-sectional study comparing different formats of probability information.Using family history information to promote healthy lifestyles and prevent diseases; a discussion of the evidence.Public health genomics and genetic test evaluation: the challenge of conducting behavioural research on the utility of lifestyle-genetic testsDevelopment and Evaluation of a Psychosocial Intervention for Children and Teenagers Experiencing Diabetes (DEPICTED): a protocol for a cluster randomised controlled trial of the effectiveness of a communication skills training programme for healthcPreventing disease through opportunistic, rapid engagement by primary care teams using behaviour change counselling (PRE-EMPT): protocol for a general practice-based cluster randomised trial.Determinants of adherence to recommendations for cancer prevention among Lynch Syndrome mutation carriers: A qualitative exploration.The very youngest scienceFrom Viruses to Russian Roulette to Dance: A Rhetorical Critique and Creation of Genetic Metaphors.Communicating genetic and genomic information: health literacy and numeracy considerationsConsultations about changing behaviour.Estimating and disclosing the risk of developing Alzheimer's disease: challenges, controversies and future directionsGenomics and health care. How genomics medicine is translated into better health care largely depends on how physicians handle this informationCo-variations and clustering of chronic disease behavioral risk factors in China: China Chronic Disease and Risk Factor Surveillance, 2007.Effect of communicating genetic and phenotypic risk for type 2 diabetes in combination with lifestyle advice on objectively measured physical activity: protocol of a randomised controlled trialA randomized trial of genetic and environmental risk assessment (GERA) for colorectal cancer risk in primary care: trial design and baseline findingsResearch issues in genetic testing of adolescents for obesity.Perceived impact of diabetes genetic risk testing among patients at high phenotypic risk for type 2 diabetes.Genetic testing for lung cancer risk: if physicians can do it, should they?Predictive genetic tests and health system costs'Genomic counseling'? Genetic counseling in the genomic era.Pharmacogenetics of smoking cessation in general practice: results from the patch II and patch in practice trialsBehavior matters.Genetics and genomics in practice: the continuum from genetic disease to genetic information in health and disease.Modelling decisions to undergo genetic testing for susceptibility to common health conditions: an ancillary study of the Multiplex InitiativeLynch syndrome: barriers to and facilitators of screening and disease managementImpact of direct-to-consumer predictive genomic testing on risk perception and worry among patients receiving routine care in a preventive health clinic.Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomicsRisk communication strategies: state of the art and effectiveness in the context of cancer genetic services.Psychological impact of genetic counseling for familial cancer: a systematic review and meta-analysis.Evaluation findings from genetics and family health history community-based workshops for African AmericansNatural settings trials--improving the introduction of clinical genetic tests.
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2001年の論文
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2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
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name
Genetic risk and behavioural change
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Genetic risk and behavioural change
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Genetic risk and behavioural change
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Genetic risk and behavioural change
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type
label
Genetic risk and behavioural change
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Genetic risk and behavioural change
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Genetic risk and behavioural change
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Genetic risk and behavioural change
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prefLabel
Genetic risk and behavioural change
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Genetic risk and behavioural change
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Genetic risk and behavioural change
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Genetic risk and behavioural change
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P2860
P3181
P1433
P1476
Genetic risk and behavioural change
@en
P2093
P2860
P304
P3181
P356
10.1136/BMJ.322.7293.1056
P407
P577
2001-04-28T00:00:00Z