scholarly article | Q13442814 |
P50 | author | Gail Geller | Q58609081 |
P2093 | author name string | Juli Murphy | |
David Kaufman | |||
Kathy Hudson | |||
Lisa LeRoy | |||
Gail Geller | |||
Joan Scott | |||
P2860 | cites work | Public expectations for return of results from large-cohort genetic research | Q28754402 |
The uneasy ethical and legal underpinnings of large-scale genomic biobanks | Q34004552 | ||
Genes, environment and the value of prospective cohort studies | Q34567044 | ||
Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework | Q34766838 | ||
The Belmont Report. Ethical principles and guidelines for the protection of human subjects of research | Q38464684 | ||
Informed consent for biorepositories: assessing prospective participants' understanding and opinions | Q40080444 | ||
Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research | Q40502508 | ||
Attitudes and perceptions of patients towards methods of establishing a DNA biobank | Q48076854 | ||
Subjects matter: a survey of public opinions about a large genetic cohort study | Q48315283 | ||
Proposed international guidelines on ethical issues in medical genetics and genetic services (part I). | Q53274862 | ||
Medicine. Reestablishing the researcher-patient compact. | Q54072717 | ||
Biobank research and the right to privacy | Q56785542 | ||
Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion | Q58672001 | ||
The case for a US prospective cohort study of genes and environment | Q59051741 | ||
Merging and emerging cohorts: necessary but not sufficient | Q79579692 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | informed consent | Q764527 |
biobank | Q864217 | ||
P304 | page(s) | 2128-34 | |
P577 | publication date | 2009-12-01 | |
P1433 | published in | American Journal of Public Health | Q4744266 |
P1476 | title | Public perspectives on informed consent for biobanking | |
P478 | volume | 99 |