Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project
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Big data, open science and the brain: lessons learned from genomicsStakeholder engagement: a key component of integrating genomic information into electronic health recordsBiobanks: importance, implications and opportunities for genetic counselorsWithin and beyond the communal turn to informed consent in industry-sponsored pharmacogenetics research: merits and challenges of community advisory boardsBroad Consent for Research With Biological Samples: Workshop ConclusionsExtracting research-quality phenotypes from electronic health records to support precision medicineOffering aggregate results to participants in genomic research: opportunities and challengesThe eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studiesConsent for genetic research in the Framingham Heart StudyGenetics and cardiovascular disease: a policy statement from the American Heart Association.Merging Electronic Health Record Data and Genomics for Cardiovascular Research: A Science Advisory From the American Heart Association.Recontacting participants for expanded uses of existing samples and data: a case study.Potential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?Unexpected findings in the exploration of African American underrepresentation in biospecimen collection and biobanksCommunity engagement in US biobanking: multiplicity of meaning and method.Structuring public engagement for effective input in policy development on human tissue biobanking'Cool! and creepy': engaging with college student stakeholders in Michigan's biobank.Research ethics. Research practice and participant preferences: the growing gulf.Current practice of public involvement activities in biomedical research and innovation: a systematic qualitative review.Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium.Genetic and ElectroNic medIcal records to predict oUtcomeS in Heart Failure patients (GENIUS-HF) - design and rationaleReasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group studyApplication of clinical text data for phenome-wide association studies (PheWASs).EngageUC: Developing an Efficient and Ethical Approach to Biobanking Research at the University of CaliforniaBiology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network.Community engagement in biobanking: Experiences from the eMERGE Network.Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.Desiderata for computable representations of electronic health records-driven phenotype algorithms.Acceptance of Asthma Pharmacogenetic Study by Children and AdultsThe role of nonverbal and verbal communication in a multimedia informed consent process.Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.'Born in Michigan? You're in the biobank': engaging population biobank participants through Facebook advertisements.Biobanking for research: a survey of patient population attitudes and understandingCharacterization of statin dose response in electronic medical records.Methods for optimizing statistical analyses in pharmacogenomics researchWhy do participants enroll in population biobank studies? A systematic literature review.Establishing and managing a periodontal biobank for research: the sharing of experience.Reducing Clinical Noise for Body Mass Index Measures Due to Unit and Transcription Errors in the Electronic Health Record.The genetics of drug efficacy: opportunities and challenges.Participants' Understanding of Informed Consent for Biobanking: A Systematic Review.
P2860
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P2860
Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project
description
2008 nî lūn-bûn
@nan
2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Community consultation and com ...... ized medicine research project
@ast
Community consultation and com ...... ized medicine research project
@en
Community consultation and com ...... ized medicine research project
@nl
type
label
Community consultation and com ...... ized medicine research project
@ast
Community consultation and com ...... ized medicine research project
@en
Community consultation and com ...... ized medicine research project
@nl
prefLabel
Community consultation and com ...... ized medicine research project
@ast
Community consultation and com ...... ized medicine research project
@en
Community consultation and com ...... ized medicine research project
@nl
P2093
P2860
P356
P1476
Community consultation and com ...... ized medicine research project
@en
P2093
Donna Chapman-Stone
Norman Fost
Philip F Giampietro
Teresa Derfus
P2860
P304
P356
10.1002/AJMG.A.32559
P407
P577
2008-12-01T00:00:00Z