A citation-based method for searching scientific literature

J Harris, K Keywood. Theor Med Bioeth 2001
Times Cited: 37







List of co-cited articles
89 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity






Genetic ignorance and reasonable paternalism.
T Takala. Theor Med Bioeth 2001
14
64

The 'right' not to know.
D E Ost. J Med Philos 1984
23
34

Genetic information, rights, and autonomy.
M Häyry, T Takala. Theor Med Bioeth 2001
13
61

Freedom and a right (not) to know.
Juha Räikkä. Bioethics 1998
8
87



The right to genetic ignorance confirmed.
Tuija Takala. Bioethics 1999
19
26

The right not to know: the case of psychiatric disorders.
Lisa Bortolotti, Heather Widdows. J Med Ethics 2011
19
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
13

"Please don't tell me". The right not to know.
Jonathan Herring, Charles Foster. Camb Q Healthc Ethics 2012
12
41

Genetic ignorance, moral obligations and social duties.
T Takala, M Häyry. J Med Philos 2000
22
18

Genetic privacy: orthodoxy or oxymoron?
A Sommerville, V English. J Med Ethics 1999
20
20


Genetic information: a joint account?
Michael Parker, Anneke M Lucassen. BMJ 2004
62
10

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
106
10

The relative importance of undesirable truths.
Lisa Bortolotti. Med Health Care Philos 2013
5
80

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
422
10




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
11
27

Why test children for adult-onset genetic diseases?
Rosamond Rhodes. Mt Sinai J Med 2006
47
8







The "right not to know" in the genomic era: time to break from tradition?
Benjamin E Berkman, Sara Chandros Hull. Am J Bioeth 2014
17
17


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
99
8






Informed consent and other fairy tales.
M A Jones. Med Law Rev 1999
23
8

Some limits of informed consent.
O O'Neill. J Med Ethics 2003
169
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
45
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
13
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
20
10


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
52
5


Who should know about our genetic makeup and why?
T Takala, H A Gylling. J Med Ethics 2000
9
22



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.