J Harris, K Keywood. Theor Med Bioeth 2001
Times Cited: 37
Times Cited: 37
Times Cited
Times Co-cited
Similarity
Genetic links, family ties, and social bonds: rights and responsibilities in the face of genetic knowledge.
R Rhodes. J Med Philos 1998
R Rhodes. J Med Philos 1998
37
In defence of ignorance: genetic information and the right not to know.
Graeme T Laurie. Eur J Health Law 1999
Graeme T Laurie. Eur J Health Law 1999
36
33
The right to remain in ignorance about genetic information--can such a right be defended in the name of autonomy?
Phillipa Malpas. N Z Med J 2005
Phillipa Malpas. N Z Med J 2005
54
Protecting and promoting privacy in an uncertain world: further defences of ignorance and the right not to know.
G T Laurie. Eur J Health Law 2000
G T Laurie. Eur J Health Law 2000
50
The right not to know: the case of psychiatric disorders.
Lisa Bortolotti, Heather Widdows. J Med Ethics 2011
Lisa Bortolotti, Heather Widdows. J Med Ethics 2011
26
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
13
"Please don't tell me". The right not to know.
Jonathan Herring, Charles Foster. Camb Q Healthc Ethics 2012
Jonathan Herring, Charles Foster. Camb Q Healthc Ethics 2012
41
18
Comment on a view favoring ignorance of genetic information: confidentiality, autonomy, beneficence and the right not to know.
M C Bottis. Eur J Health Law 2000
M C Bottis. Eur J Health Law 2000
44
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.
S Creighton, E W Almqvist, D MacGregor, B Fernandez, H Hogg, J Beis, J P Welch, C Riddell, R Lokkesmoe, M Khalifa,[...]. Clin Genet 2003
S Creighton, E W Almqvist, D MacGregor, B Fernandez, H Hogg, J Beis, J P Welch, C Riddell, R Lokkesmoe, M Khalifa,[...]. Clin Genet 2003
10
Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
10
Privacy and disclosure in medical genetics examined in an ethics of care.
Dorothy C Wertz, John C Fletcher. Bioethics 1991
Dorothy C Wertz, John C Fletcher. Bioethics 1991
13
Challenging medical-legal norms. The role of autonomy, confidentiality, and privacy in protecting individual and familial group rights in genetic information.
G T Laurie. J Leg Med 2001
G T Laurie. J Leg Med 2001
33
17
Concern, pressure and lack of knowledge affect choice of not wanting to know high-risk status.
Ulrica Swartling, Stefan Eriksson, Johnny Ludvigsson, Gert Helgesson. Eur J Hum Genet 2007
Ulrica Swartling, Stefan Eriksson, Johnny Ludvigsson, Gert Helgesson. Eur J Hum Genet 2007
27
Is there a case in favour of predictive genetic testing in young children?
S Robertson, J Savulescu. Bioethics 2001
S Robertson, J Savulescu. Bioethics 2001
8
The right not to know and preimplantation genetic diagnosis for Huntington's disease.
E Asscher, B-J Koops. J Med Ethics 2010
E Asscher, B-J Koops. J Med Ethics 2010
17
To know or not to know: a review of behaviour and suicidal ideation in preclinical Huntington's disease.
Tarja-Brita Robins Wahlin. Patient Educ Couns 2007
Tarja-Brita Robins Wahlin. Patient Educ Couns 2007
8
Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing.
Megan Allyse, Marsha Michie. Trends Biotechnol 2013
Megan Allyse, Marsha Michie. Trends Biotechnol 2013
8
Recognizing the Right Not to Know: Conceptual, Professional, and Legal Implications.
Graeme Laurie. J Law Med Ethics 2014
Graeme Laurie. J Law Med Ethics 2014
16
The "right not to know" in the genomic era: time to break from tradition?
Benjamin E Berkman, Sara Chandros Hull. Am J Bioeth 2014
Benjamin E Berkman, Sara Chandros Hull. Am J Bioeth 2014
17
The right not to know--worthy of preservation any longer? An ethical perspective.
T Austad. Clin Genet 1996
T Austad. Clin Genet 1996
37
To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
8
Testing for the Huntington gene: a right to know, a right not to know, or a duty to know.
M W Shaw. Am J Med Genet 1987
M W Shaw. Am J Med Genet 1987
11
Right not to know or duty to know? Prenatal screening for polycystic renal disease.
R Kielstein, H M Sass. J Med Philos 1992
R Kielstein, H M Sass. J Med Philos 1992
23
Consent to epistemic interventions: a contribution to the debate on the right (not) to know.
Niels Nijsingh. Med Health Care Philos 2016
Niels Nijsingh. Med Health Care Philos 2016
100
A philosophical and critical analysis of the European convention of bioethics.
G Hottois. J Med Philos 2000
G Hottois. J Med Philos 2000
28
Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium.
P S Harper, C Lim, D Craufurd. J Med Genet 2000
P S Harper, C Lim, D Craufurd. J Med Genet 2000
5
The new genetics and its consequences for family, kinship, medicine and medical genetics.
Kaja Finkler, Cécile Skrzynia, James P Evans. Soc Sci Med 2003
Kaja Finkler, Cécile Skrzynia, James P Evans. Soc Sci Med 2003
5
Bioethical theory and practice in genetic screening for type 1 diabetes.
U Gustafsson Stolt, J Ludvigsson, P E Liss, T Svensson. Med Health Care Philos 2003
U Gustafsson Stolt, J Ludvigsson, P E Liss, T Svensson. Med Health Care Philos 2003
15
Information and informed consent in a longitudinal screening involving children: a questionnaire survey.
Ulrica Gustafsson Stolt, Gert Helgesson, Per-Erik Liss, Tommy Svensson, Johnny Ludvigsson. Eur J Hum Genet 2005
Ulrica Gustafsson Stolt, Gert Helgesson, Per-Erik Liss, Tommy Svensson, Johnny Ludvigsson. Eur J Hum Genet 2005
10
Autonomy, respect, and genetic information policy: a reply to Tuija Takala and Matti Häyry.
Rosamond Rhodes. J Med Philos 2000
Rosamond Rhodes. J Med Philos 2000
25
Men's decision-making about predictive BRCA1/2 testing: the role of family.
N Hallowell, A Ardern-Jones, R Eeles, C Foster, A Lucassen, C Moynihan, M Watson. J Genet Couns 2005
N Hallowell, A Ardern-Jones, R Eeles, C Foster, A Lucassen, C Moynihan, M Watson. J Genet Couns 2005
5
Predictive genetic test decisions for Huntington's disease: context, appraisal and new moral imperatives.
Sandra D Taylor. Soc Sci Med 2004
Sandra D Taylor. Soc Sci Med 2004
5
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.