about
Personal genome sequencing: current approaches and challengesGenome-wide association studies: a primerRisk assessment and communication tools for genotype associations with multifactorial phenotypes: the concept of "edge effect" and cultivating an ethical bridge between omics innovations and societyData sharing in genomics--re-shaping scientific practiceInformed consent in the genomics eraEvolving approaches to the ethical management of genomic dataEyes wide open: the personal genome project, citizen science and veracity in informed consentBiobanks in the era of personalized medicine: objectives, challenges, and innovation: OverviewBetween Openness and Privacy in GenomicsThe tension between data sharing and the protection of privacy in genomics researchCommunicating results in post-Belmont era biomonitoring studies: lessons from genetics and neuroimaging researchAttitudes of research participants and the general public towards genomic data sharing: a systematic literature reviewComprehensive genomic studies: emerging regulatory, strategic, and quality assurance challenges for biorepositoriesIdentifiability in biobanks: models, measures, and mitigation strategiesA public resource facilitating clinical use of genomesQuantification of private information leakage from phenotype-genotype data: linking attacksImproving the informed consent process in international collaborative rare disease research: effective consent for effective research.A global network for investigating the genomic epidemiology of malariaGenomics and privacy: implications of the new reality of closed data for the fieldA vision for ubiquitous sequencingAn "Ethical Moment" in Data SharingThe risk of re-identification versus the need to identify individuals in rare disease researchAddressing Benefits, Risks and Consent in Next Generation Sequencing StudiesFacilitating a culture of responsible and effective sharing of cancer genome dataInternational Charter of principles for sharing bio-specimens and dataBalancing Benefits and Risks of Immortal Data: Participants' Views of Open Consent in the Personal Genome ProjectDoes science need bioethicists? Ethics and science collaboration in biomedical researchEthical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in JapanMultidisciplinary approach to genomics research in Africa: the AfriCRAN modelEpigenome data release: a participant-centered approach to privacy protectionChallenges of web-based personal genomic data sharingSystems Medicine 2.0: potential benefits of combining electronic health care records with systems science modelsSecureMA: protecting participant privacy in genetic association meta-analysisEvaluating the consent preferences of UK research volunteers for genetic and clinical studiesRoutes for breaching and protecting genetic privacyDisentangling public participation in science and biomedicineRevisiting respect for persons in genomic researchOur genomes today: time to be clearInformed Consent in Genome-Scale Research: What Do Prospective Participants Think?'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care
P2860
Q22065782-5548B241-7A6E-4D49-978D-DFC554DA0798Q24273247-D1A384C4-EA1B-4E3A-8F97-BDEEA7057655Q24289220-9F8DC422-1824-4579-BDDF-3A9F1CFCDEB5Q24550016-0e851dff-4547-beb7-dc1f-14634262b3deQ24550536-4F109BF3-D14D-4E82-916A-BDBB6F3C40C2Q24618993-DD989AAB-59F1-4428-A807-93E4DB9A112CQ24634042-9BD91BA9-4634-4F53-A106-B5C8F4F089C3Q26767428-B9334BCE-02FE-4EAD-8B9F-4303BC478DBEQ26772241-5923CE3C-A83F-4170-ABD8-3DBD770BB761Q26866269-98450DA4-07F1-441F-9112-B80E4B19708AQ27008196-24303335-FFB9-4978-AEEC-0C7219308DEBQ27008350-EA1E47BB-921A-4824-8E9A-0533F1801070Q27009141-CA8AD3C0-BAC6-4141-BAD7-822B70748C34Q27010356-25B4FDD9-A451-4DDD-A9FF-C583A42A100DQ27133763-8978E4C0-3D65-45CE-9E1D-2240E4CE5783Q27313579-100C2454-51DF-49AC-897A-114BE9E881EEQ27324539-076178AB-C960-4F57-AE29-DCE3C97A0B5CQ28031370-2FCEDB9A-ECFF-4A57-9748-ECC5B079EA35Q28254700-212E84C9-1742-4C6A-84DB-3F4E2429020EQ28268019-9855C3B2-66C7-41DF-9F74-C88A0727BBEAQ28587951-6A34B26B-B474-428B-8CEC-A810372C6BD2Q28595728-4309E954-4D1B-4748-8976-646D50695DD5Q28596875-DC0371F5-A794-4712-9519-4FB0A8EBA381Q28597289-5129453B-104E-4619-8C39-21F92BDD6643Q28602512-1E3E3720-B1A4-45D9-BFBD-967B7DFE2375Q28602597-77C8D94F-8DBB-4AB4-9B97-25262C2D27E8Q28607116-C8F93F14-EE27-4574-B19E-0A3FDB8C9437Q28607430-B95389D9-3991-4351-9E25-6E5F10A48B96Q28611197-72392CC7-DA40-40A7-A0F8-1C2C2239C058Q28646976-3BB71E67-F604-4F18-911A-C3B69F92D246Q28647937-0EB64A02-3D81-4115-8796-328AB6FA7171Q28650276-7520FC48-9E89-4CDC-8D52-5E4C4CA9702DQ28652195-F245AAB1-9A86-48C6-877A-43D9AFEBFB4AQ28652534-664BC472-9627-4BB8-A7B6-59F9ECB272D4Q28656170-EE7C4C5A-1166-4F33-9C5B-90846EDDD7B1Q28660335-6401B1E2-2A13-40DB-AEEF-1A58A7809F16Q28660341-7CF8CDAC-67A0-4731-B96F-5A6A0D1CBC0FQ28679291-E06248BE-7E64-4A77-91EC-AF22900757BCQ28704258-41A79062-5FA2-4ED2-A78B-7BA06C52B445Q28711804-F9301881-A354-4D2F-ABDB-FAFAF8F20BFB
P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին 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
From genetic privacy to open consent
@ast
From genetic privacy to open consent
@en
From genetic privacy to open consent
@nl
type
label
From genetic privacy to open consent
@ast
From genetic privacy to open consent
@en
From genetic privacy to open consent
@nl
prefLabel
From genetic privacy to open consent
@ast
From genetic privacy to open consent
@en
From genetic privacy to open consent
@nl
P2860
P50
P3181
P356
P1476
From genetic privacy to open consent
@en
P2093
Daniel B Vorhaus
P2860
P2888
P304
P3181
P356
10.1038/NRG2360
P407
P577
2008-05-01T00:00:00Z
P5875
P6179
1018303410