Informed consent for population-based research involving genetics.
about
Strangers at the benchside: research ethics consultationDNA databanks and consent: a suggested policy option involving an authorization modelThe role of genetic polymorphisms in environmental health.Methodologic and logistic issues in conducting longitudinal birth cohort studies: lessons learned from the Centers for Children's Environmental Health and Disease Prevention Research.The tension between data sharing and the protection of privacy in genomics researchIncidental findings in genetics research using archived DNAGenetic research participation in a young adult community sampleAttitudes toward genetic research review: results from a survey of human genetics researchersHandling ethical, legal and social issues in birth cohort studies involving genetic research: responses from studies in six countriesPublic expectations for return of results from large-cohort genetic researchAmyotrophic lateral sclerosis: an emerging era of collaborative gene discoveryNot so simple: a quasi-experimental study of how researchers adjudicate genetic research resultsActive choice but not too active: public perspectives on biobank consent models.Epidemiology and genetics of common mental disorders in the general population: the PEGASUS-Murcia project.Valid consent for genomic epidemiology in developing countriesGenome wide association for substance dependence: convergent results from epidemiologic and research volunteer samples.Potential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?Personal characteristics of older primary care patients who provide a buccal swab for apolipoprotein E testing and banking of genetic material: the spectrum studyParticipant characteristics that influence consent for genetic research in a population-based survey: the Baltimore epidemiologic catchment area follow-upPerspectives on human microbiome research ethicsTailoring the process of informed consent in genetic and genomic researchProspective biorepository participants' perspectives on access to research results.Bridging consent: from toll bridges to lift bridges?Biobanking, consent, and commercialization in international genetics research: the Type 1 Diabetes Genetics Consortium.Experiences and attitudes of genome investigators regarding return of individual genetic test results.Managing incidental findings and research results in genomic research involving biobanks and archived data sets.Receiving a summary of the results of a trial: qualitative study of participants' views.Disclosing individual genetic results to research participants.Considering the nature of individual research results.Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample.Genetic research with stored biological materials: ethics and practice.Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working groupElements of informed consent for pharmacogenetic research; perspective of the pharmacogenetics working group.Patient perspectives on group benefits and harms in genetic research.Returning individual research results: development of a cancer genetics education and risk communication protocolHuman nutrition and food research: opportunities and challenges in the post-genomic era.Informed consent in genomics and genetic research.Monitoring ethical, legal, and social issues in developing population genetic databases.Eating disorders, serotonin transporter polymorphisms and potential treatment response.Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility
P2860
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P2860
Informed consent for population-based research involving genetics.
description
2001 nî lūn-bûn
@nan
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
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
@wuu
name
Informed consent for population-based research involving genetics.
@ast
Informed consent for population-based research involving genetics.
@en
Informed consent for population-based research involving genetics.
@nl
type
label
Informed consent for population-based research involving genetics.
@ast
Informed consent for population-based research involving genetics.
@en
Informed consent for population-based research involving genetics.
@nl
prefLabel
Informed consent for population-based research involving genetics.
@ast
Informed consent for population-based research involving genetics.
@en
Informed consent for population-based research involving genetics.
@nl
P2093
P356
P1476
Informed consent for population-based research involving genetics.
@en
P2093
L M Beskow
L O Gostin
V B Penchaszadeh
P304
P356
10.1001/JAMA.286.18.2315
P407
P577
2001-11-01T00:00:00Z