about
Big Data: the challenge for small research groups in the era of cancer genomicsEthical and deontological issues in Transfusion MedicineStakeholders' perspectives on biobank-based genomic research: systematic review of the literatureScientists' perspectives on consent in the context of biobanking research.Gene mutations responsible for primary immunodeficiency disorders: A report from the first primary immunodeficiency biobank in IranInternational Charter of principles for sharing bio-specimens and dataFair Shares and Sharing Fairly: A Survey of Public Views on Open Science, Informed Consent and Participatory Research in BiobankingPractice variation across consent templates for biobank research. a survey of German biobanksThe Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.Patient/family views on data sharing in rare diseases: study in the European LeukoTreat project.Bio-collections in autism research.Consent for use of clinical leftover biosample: a survey among Chinese patients and the general publicHypothetical and factual willingness to participate in biobank researchBiobanking research on oncological residual material: a framework between the rights of the individual and the interest of society.Community engagement for big epidemiology: deliberative democracy as a tool.Ethical aspects of human biobanks: a systematic review.Gut Health in the era of the human gut microbiota: from metaphor to biovalue.Bioethical considerations in developing a biorepository for the Pneumonia Etiology Research for Child Health projectDeveloping a policy for paediatric biobanks: principles for good practice.Athlome Project Consortium: a concerted effort to discover genomic and other "omic" markers of athletic performance.Public support and consent preference for biomedical research and biobanking in JordanContributing to research via biobanks: what it means to cancer patientsA biorepository for ophthalmic surgical specimens.Cancer patient perceptions about biobanking and preferred timing of consent.The interface of population-based cancer registries and biobanks in etiological and clinical research--current and future perspectives.The Bio-PIN: a concept to improve biobanking.The utility of collaborative biobanks for cardiovascular research.Application of metabolomics approaches to the study of respiratory diseases.Participation in biobanks for research by incapacitated adults: review and discussion of current guidelines.Genomic medicine and risk prediction across the disease spectrum.Legal & ethical compliance when sharing biospecimen.Developments in biospecimen research.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.Where should we draw the line between quality of care and other ethical concerns related to medical registries and biobanks?Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership.Ethically sustainable governance in the biobanking of eggs and embryos for research."Forward-Thinking" in U.S. Biobanking.Chinese biobanks: present and future.Attitudes towards biosample donation in andrology patients.Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Ethics and biobanks.
@en
Ethics and biobanks.
@nl
type
label
Ethics and biobanks.
@en
Ethics and biobanks.
@nl
prefLabel
Ethics and biobanks.
@en
Ethics and biobanks.
@nl
P2860
P921
P356
P1476
Ethics and biobanks.
@en
P2093
M G Hansson
P2860
P2888
P356
10.1038/SJ.BJC.6604795
P407
P577
2008-11-25T00:00:00Z