Autonomy and a right not to know

J Husted, M Chadwick - The right to know and the right not to …, 2014 - books.google.com
Genetics and diseases of genetic origin inescapably involve families. Thus genetic
information obtained by testing one person may contain information of the same kind on one …

Protecting genetic information: a comparison of normative approaches

P Kosseim, M Letendre, BM Knoppers - GenEdit, 2004 - papyrus.bib.umontreal.ca
The increasing use of genetic information has emerged as an important concern worldwide
as scientific and technological advances continue to advance at lightening speed and as …

[图书][B] Genetic discrimination and genetic privacy in a comparative perspective

JH Gerards, AW Heringa, HL Janssen - 2005 - books.google.com
During the last decades, a better understanding of the influence of genetic factors on the
onset of illness and disease has evolved. Unfortunately, however, the information revealed …

[HTML][HTML] The ethical use of existing samples for genome research

OF Bathe, AL McGuire - Genetics in Medicine, 2009 - Elsevier
Modern biobanking efforts consist of prospective collections of tissues linked to clinical data
for patients who have given informed consent for the research use of their specimens and …

Ethical and practical challenges surrounding genetic and genomic research in developing countries

A Nyika - Acta Tropica, 2009 - Elsevier
The nature of some potential benefits and risks associated with genetic research is different
from the types of potential benefits and risks associated with other types of health research …

Relative responsibilities: is there an obligation to discuss genomics research participation with family members?

P Boddington - Public Health Genomics, 2010 - karger.com
One of the many ethical challenges presented by research in genomics is that, although
informed consent to research has traditionally been a matter for the individual participant …

Informed consent in direct‐to‐consumer personal genome testing: the outline of a model between specific and generic consent

EM Bunnik, ACJW Janssens, MHN Schermer - Bioethics, 2014 - Wiley Online Library
Broad genome‐wide testing is increasingly finding its way to the public through the online
direct‐to‐consumer marketing of so‐called personal genome tests. Personal genome tests …

Consent codes: upholding standard data use conditions

SOM Dyke, AA Philippakis, J Rambla De Argila… - PLoS …, 2016 - journals.plos.org
Consent Codes: Upholding Standard Data Use Conditions | PLOS Genetics Skip to main
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Human genetic banking and the limits of informed consent

G Williams, D Schroeder - Reconfiguring Nature, 2017 - taylorfrancis.com
In the medical context human genetic banking has attracted a quite different discourse, with
individual rights at the forefront: those relating to the informed consent of actual and potential …

Genetic Information Access, a Legal Perspective: A Duty to Know or a Right Not to Know, and a Duty or Option to Warn?

T Lemmens, L Luther, M Hoy - eLS, 2008 - Wiley Online Library
It is often argued that concern with basic personal privacy suggests that individuals should
be allowed to decide in isolation whether to obtain genetic information through testing and …