review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Alice K. Hawkins | |
P2860 | cites work | Translating pharmacogenomics: challenges on the road to the clinic | Q21092371 |
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays | Q21092481 | ||
Research ethics recommendations for whole-genome research: consensus statement | Q21145862 | ||
From genetic privacy to open consent | Q24550752 | ||
Mutation detection in the ABCC6 gene and genotype-phenotype analysis in a large international case series affected by pseudoxanthoma elasticum | Q24648254 | ||
DNA databanks and consent: a suggested policy option involving an authorization model | Q24795476 | ||
Genomic medicine: considerations for health professionals and the public | Q27499767 | ||
Evolutionary concepts in biobanking - the BC BioLibrary | Q28392339 | ||
Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project | Q28756483 | ||
Democratising access to genetic services. | Q30353330 | ||
Commercial biobanks and genetic research: ethical and legal issues | Q30948908 | ||
The charitable trust as a model for genomic biobanks | Q30988245 | ||
Structuring public engagement for effective input in policy development on human tissue biobanking | Q33869885 | ||
The uneasy ethical and legal underpinnings of large-scale genomic biobanks | Q34004552 | ||
Genebanks: A Comparison of Eight Proposed International Genetic Databases | Q34197070 | ||
Potential harms, anonymization, and the right to withdraw consent to biobank research | Q34429768 | ||
Biobanking for Europe | Q34584168 | ||
Trends in ethical and legal frameworks for the use of human biobanks | Q34658049 | ||
Ethical, legal, and social implications of biobanks for genetics research | Q34763998 | ||
Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework | Q34766838 | ||
Broadening consent--and diluting ethics? | Q34933645 | ||
Monitoring ethical, legal, and social issues in developing population genetic databases | Q35582392 | ||
The emergence of epidemiology in the genomics age. | Q35866648 | ||
Securing our genetic health: engendering trust in UK Biobank | Q36078686 | ||
Biobanking: international norms | Q36150035 | ||
Should donors be allowed to give broad consent to future biobank research? | Q36410751 | ||
From hype to mothballs in four years: troubles in the development of large-scale DNA biobanks in Europe | Q36495112 | ||
National population-based biobanks for genetic research | Q36782922 | ||
Ethics and biobanks | Q37080971 | ||
Informed consent in biobank research: a deliberative approach to the debate | Q37354492 | ||
Biobanking for epidemiological research and public health | Q40181846 | ||
The social and ethical issues of post-genomic human biobanks | Q42639498 | ||
Biobanks, bioethics and concepts of donated blood in the UK. | Q45951412 | ||
'Biobanks' "engagements": engendering trust or engineering consent?'. | Q47153106 | ||
Navigating an ethical patchwork--human gene banks | Q48139225 | ||
Engaging the public on biobanks: outcomes of the BC biobank deliberation | Q48286546 | ||
Community engagement and informed consent in the International HapMap project. | Q53234473 | ||
Biobanks. Population databases boom, from Iceland to the U.S. | Q53408965 | ||
Population Biobanks: The Ethical Gravity of Informed Consent | Q56769692 | ||
‘I'm not Really Read up on Genetics’: Biobanks and the Social Context of Informed Consent | Q56769695 | ||
Informed consent in a changing environment | Q56785700 | ||
Marshfield Clinic Personalized Medicine Research Project (PMRP): design, methods and recruitment for a large population-based biobank | Q57194133 | ||
Biobanks | Q57261729 | ||
Shifting Subject Positions | Q57632732 | ||
The emergence of an ethical duty to disclose genetic research results: international perspectives | Q58674081 | ||
Nanotechnology, Governance, and Public Deliberation: What Role for the Social Sciences? | Q73180417 | ||
Further plans announced for national biobanks | Q82833198 | ||
Banking expectations: the promises and problems of biobanks | Q88790360 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | data sharing | Q5227350 |
biobank | Q864217 | ||
genetic counseling | Q1124169 | ||
tissue bank | Q2893478 | ||
P304 | page(s) | 423-9 | |
P577 | publication date | 2010-08-03 | |
2010-10-01 | |||
P1433 | published in | Journal of Genetic Counseling | Q6295247 |
P1476 | title | Biobanks: importance, implications and opportunities for genetic counselors | |
Biobanks: Importance, Implications and Opportunities for Genetic Counselors | |||
P478 | volume | 19 |
Q21202161 | "Who owns your poop?": insights regarding the intersection of human microbiome research and the ELSI aspects of biobanking and related studies |
Q39143901 | "Why throw away something useful?": Attitudes and opinions of people treated for bipolar disorder and their relatives on organ and tissue donation. |
Q36983135 | A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs |
Q37323166 | A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases |
Q57156796 | Banking brains: a pre-mortem "how to" guide to successful donation |
Q28662280 | Biobanking: The Melding of Research with Clinical Care |
Q26767428 | Biobanks in the era of personalized medicine: objectives, challenges, and innovation: Overview |
Q35055868 | Ethical aspects of human biobanks: a systematic review |
Q42690293 | Ethical considerations in biobanks: how a public health ethics perspective sheds new light on old controversies |
Q28686910 | Formative research on perceptions of biobanking: what community members think |
Q28654959 | Newspaper coverage of biobanks |
Q40571766 | Participants' Role Expectations in Genetics Research and Re-consent: Revising the Theory and Methods of Mental Models Research Relating to Roles. |
Q39044592 | Perceptions of tissue storage in a dementia population among spouses and offspring |
Q64067205 | Population's perspectives toward biobanks in scientific research: a study from Jordan |
Q34074073 | REXIC Project: Retrospective Cross-Sectional Study of Documentation of Informed Consent for Research Biobanking in A Public Research and Teaching Hospital. |
Q37041787 | Raising Genomic Citizens: Adolescents and the Return of Secondary Genomic Findings |
Q42968231 | Returning Results: Let's Be Honest! |
Q90419989 | Sustainability in Biobanking |
Q47768267 | The Genetic Counselor's Role in Managing Ethical Dilemmas Arising in the Laboratory Setting |
Q47765271 | The Precision Medicine Nation |
Q48672150 | The sense of responsibility in the context of professional activities in Medical Genetics |
Q37876693 | Using electronic health records to drive discovery in disease genomics |