A citation-based method for searching scientific literature

R Andorno. J Med Ethics 2004
Times Cited: 90







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



Times Cited
  Times     Co-cited
Similarity


Ignorance, information and autonomy.
J Harris, K Keywood. Theor Med Bioeth 2001
37
40

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
16




Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information.
N Hallowell, C Foster, R Eeles, A Ardern-Jones, V Murday, M Watson. J Med Ethics 2003
110
10

Genetic professionals' reports of nondisclosure of genetic risk information within families.
Angus Clarke, Martin Richards, Lauren Kerzin-Storrar, Jane Halliday, Mary Anne Young, Sheila A Simpson, Katie Featherstone, Karen Forrest, Anneke Lucassen, Patrick J Morrison,[...]. Eur J Hum Genet 2005
68
11

The right not to know: the case of psychiatric disorders.
Lisa Bortolotti, Heather Widdows. J Med Ethics 2011
20
40

To tell or not to tell: barriers and facilitators in family communication about genetic risk.
K Forrest, S A Simpson, B J Wilson, E R van Teijlingen, L McKee, N Haites, E Matthews. Clin Genet 2003
222
7

The 'right' not to know.
D E Ost. J Med Philos 1984
23
30


The "duty to warn" a patient's family members about hereditary disease risks.
Kenneth Offit, Elizabeth Groeger, Sam Turner, Eve A Wadsworth, Mary A Weiser. JAMA 2004
145
6


Freedom and a right (not) to know.
Juha Räikkä. Bioethics 1998
8
75


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
425
6


"Please don't tell me". The right not to know.
Jonathan Herring, Charles Foster. Camb Q Healthc Ethics 2012
12
50


Medical Geneticists' duty to warn at-risk relatives for genetic disease.
Marni J Falk, R Beth Dugan, Mary Ann O'Riordan, Anne L Matthews, Nathaniel H Robin. Am J Med Genet A 2003
54
9

Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients.
Erna Claes, Gerry Evers-Kiebooms, Andrea Boogaerts, Marleen Decruyenaere, Lieve Denayer, Eric Legius. Am J Med Genet A 2003
148
5



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

Challenges in the clinical application of whole-genome sequencing.
Kelly E Ormond, Matthew T Wheeler, Louanne Hudgins, Teri E Klein, Atul J Butte, Russ B Altman, Euan A Ashley, Henry T Greely. Lancet 2010
145
5

Confidentiality and sharing genetic information with relatives.
Anneke Lucassen, Michael Parker. Lancet 2010
17
29

Genetic information: a joint account?
Michael Parker, Anneke M Lucassen. BMJ 2004
62
8

Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
69
7

Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
204
5

The "right not to know" in the genomic era: time to break from tradition?
Benjamin E Berkman, Sara Chandros Hull. Am J Bioeth 2014
18
27

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
221
5


Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
720
5

Family communication about positive BRCA1 and BRCA2 genetic test results.
Bobbi McGivern, Jessica Everett, Geoffrey G Yager, Robert C Baumiller, Amanda Hafertepen, Howard M Saal. Genet Med 2004
82
4

Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience.
R Beth Dugan, Georgia L Wiesner, Eric T Juengst, Maryann O'Riordan, Anne L Matthews, Nathaniel H Robin. Am J Med Genet C Semin Med Genet 2003
65
6




Genetic ignorance and reasonable paternalism.
T Takala. Theor Med Bioeth 2001
14
28


Facilitating family communication about predictive genetic testing: probands' perceptions.
Clara L Gaff, Veronica Collins, Tiffany Symes, Jane Halliday. J Genet Couns 2005
72
5


Predictive testing for Huntington's disease.
Aad Tibben. Brain Res Bull 2007
77
5


Communicating genetic information in families--a review of guidelines and position papers.
Laura E Forrest, Martin B Delatycki, Loane Skene, MaryAnne Aitken. Eur J Hum Genet 2007
79
5

Genetic testing: psychological aspects and implications.
Caryn Lerman, Robert T Croyle, Kenneth P Tercyak, Heidi Hamann. J Consult Clin Psychol 2002
157
4

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
4


A systematic review of perceived risks, psychological and behavioral impacts of genetic testing.
Jodi T Heshka, Crystal Palleschi, Heather Howley, Brenda Wilson, Philip S Wells. Genet Med 2008
206
4



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.