Delivery of genomic medicine for common chronic adult diseases: a systematic review.
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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 disordersEffects of communicating DNA-based disease risk estimates on risk-reducing behavioursEducation and personalized genomics: deciphering the public’s genetic health reportThe impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysisA national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicineGenomic medicine: considerations for health professionals and the publicUsing lifetime risk estimates in personal genomic profiles: estimation of uncertaintyAn Assessment of Family History Information Captured in an Electronic Health RecordPractical considerations in genomic decision support: The eMERGE experiencePredictive and prognostic molecular markers for cancer medicinePlanning for translational research in genomicsMedical student preparedness for an era of personalized medicine: findings from one US medical schoolAre physicians prepared for whole genome sequencing? a qualitative analysisGenetics in health care: an overview of current and emerging models.Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectivesLay perceptions of predictive testing for diabetes based on DNA test results versus family history assessment: a focus group studyEvaluating genetic counseling for individuals with schizophrenia in the molecular ageThe MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicineProposed roadmap to stepwise integration of genetics in family medicine and clinical research.Genetic Knowledge Among Participants in the Coriell Personalized Medicine CollaborativeGenetic data sharing and privacy.Health screening behaviors among adults with hereditary hemorrhagic telangiectasia in North AmericaA toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.Evaluation of LOINC for representing constitutional cytogenetic test result reports.Considerations for designing a prototype genetic test for use in translational research."I am pregnant and my husband has diabetes. Is there a risk for my child?" A qualitative study of questions asked by email about the role of genetic susceptibility to diabetesLoss-of-function CYP2C9 variants: finding the correct clinical role for Type 2 diabetes pharmacogenetic testingDoes personal genome testing drive service utilization in an adult preventive medicine clinic?Familial risk of cancer and knowledge and use of genetic testing.Pharmacogenomic knowledge gaps and educational resource needs among physicians in selected specialties.Addressing the challenges of the clinical application of pharmacogenetic testingJumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 1. Fundamental Concepts in Molecular Genetics.Practical considerations to guide development of access controls and decision support for genetic information in electronic medical recordsIdentification of Novel Susceptibility Genes for Breast Cancer - Genome-Wide Association Studies or Evaluation of Candidate Genes?Realities and expectations of pharmacogenomics and personalized medicine: impact of translating genetic knowledge into clinical practice.Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and designGrowing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.Breast cancer susceptibility: current knowledge and implications for genetic counsellingEffect 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 trialImplementation and outcomes of telephone disclosure of clinical BRCA1/2 test results.
P2860
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P2860
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
@en
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
@nl
type
label
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
@en
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
@nl
prefLabel
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
@en
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
@nl
P2093
P356
P1476
Delivery of genomic medicine for common chronic adult diseases: a systematic review.
@en
P2093
Maren T Scheuner
Paul G Shekelle
Pauline Sieverding
P304
P356
10.1001/JAMA.299.11.1320
P407
P577
2008-03-01T00:00:00Z