Biobanks. Population databases boom, from Iceland to the U.S.
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Prospective study of one million deaths in India: rationale, design, and validation resultsPublic expectations for return of results from large-cohort genetic researchTechnical and policy approaches to balancing patient privacy and data sharing in clinical and translational researchChallenges to informed consent.Logistic-AFT location-scale mixture regression models with nonsusceptibility for left-truncated and general interval-censored data.Construction of atorvastatin dose-response relationships using data from a large population-based DNA biobank.The Genome Austria Tissue Bank (GATiB).Establishment of a cervical cancer bio-bank for the Chinese population: from project-based sample collection to routine management.A common CNR1 (cannabinoid receptor 1) haplotype attenuates the decrease in HDL cholesterol that typically accompanies weight gain.National Biobanks: Clinical Labor, Risk Production, and the Creation of BiovalueCharacteristics of responders to a request for a buccal cell specimen among survivors of childhood cancer and their siblingsIntegrating heterogeneous high-throughput data for meta-dimensional pharmacogenomics and disease-related studiesBeliefs and attitudes towards participating in genetic research - a population based cross-sectional study.Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework.Ethical aspects of human biobanks: a systematic review.Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group studyBuilding on relationships of trust in biobank research.Monitoring ethical, legal, and social issues in developing population genetic databases.Use of an electronic medical record for the identification of research subjects with diabetes mellitus.From pharmacogenetics to personalized medicine: a vital need for educating health professionals and the community.Biobank governance: heterogeneous modes of ordering and democratization.Bodily rights and property rights.Biobanks for genomics and genomics for biobanks.Public views on the donation and use of human biological samples in biomedical research: a mixed methods study.Biobanking for research: a survey of patient population attitudes and understandingQuantification of the clinical modifiers impacting high-density lipoprotein cholesterol in the community: Personalized Medicine Research Project.Characterization of statin dose response in electronic medical records.Ethical aspects of participation in the database of genotypes and phenotypes of the National Center for Biotechnology Information: the Cancer and Leukemia Group B Experience.Biobank governance: trends and perspectives.Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?The Marshfield Clinic Personalized Medicine Research Project: 2008 scientific update and lessons learned in the first 6 yearsGenetics of Dizygotic Twinning: A Feasibility Study for a Biobank
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P2860
Biobanks. Population databases boom, from Iceland to the U.S.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
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2002年學術文章
@zh-hant
name
Biobanks. Population databases boom, from Iceland to the U.S.
@en
Biobanks. Population databases boom, from Iceland to the U.S.
@nl
type
label
Biobanks. Population databases boom, from Iceland to the U.S.
@en
Biobanks. Population databases boom, from Iceland to the U.S.
@nl
prefLabel
Biobanks. Population databases boom, from Iceland to the U.S.
@en
Biobanks. Population databases boom, from Iceland to the U.S.
@nl
P921
P1433
P1476
Biobanks. Population databases boom, from Iceland to the U.S.
@en
P304
P356
10.1126/SCIENCE.298.5596.1158
P407
P577
2002-11-01T00:00:00Z