A citation-based method for searching scientific literature

Fiona A Miller, Mita Giacomini, Catherine Ahern, Jason S Robert, Sonya de Laat. BMC Med Ethics 2008
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
204
42


The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur J Hum Genet 2006
196
32

What is a meaningful result? Disclosing the results of genomic research in autism to research participants.
Fiona Alice Miller, Robin Zoe Hayeems, Jessica Peace Bytautas. Eur J Hum Genet 2010
46
32

Duty to disclose what? Querying the putative obligation to return research results to participants.
F A Miller, R Christensen, M Giacomini, J S Robert. J Med Ethics 2008
90
28

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
221
28

Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.
Ebony B Bookman, Aleisha A Langehorne, John H Eckfeldt, Kathleen C Glass, Gail P Jarvik, Michael Klag, Greg Koski, Arno Motulsky, Benjamin Wilfond, Teri A Manolio,[...]. Am J Med Genet A 2006
159
28

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
469
25

Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
156
21

Informing study participants of research results: an ethical imperative.
Conrad V Fernandez, Eric Kodish, Charles Weijer. IRB 2003
133
21

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
159
21

Returning genetic research results to individuals: points-to-consider.
Gaile Renegar, Christopher J Webster, Steffen Stuerzebecher, Lea Harty, Susan E Ide, Beth Balkite, Taryn A Rogalski-Salter, Nadine Cohen, Brian B Spear, Diane M Barnes,[...]. Bioethics 2006
69
21

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
21

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
133
21

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
281
21

Communication of biobanks' research results: what do (potential) participants want?
Tineke M Meulenkamp, Sjef K Gevers, Jasper A Bovenberg, Gerard H Koppelman, Astrid van Hylckama Vlieg, Ellen M A Smets. Am J Med Genet A 2010
66
21






Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results.
Robin Zoe Hayeems, Fiona Alice Miller, Li Li, Jessica Peace Bytautas. Eur J Hum Genet 2011
24
20

The therapeutic misconception: informed consent in psychiatric research.
P S Appelbaum, L H Roth, C Lidz. Int J Law Psychiatry 1982
378
14

Best laid plans for offering results go awry.
Lisa S Parker. Am J Bioeth 2006
23
17


Considerations and costs of disclosing study findings to research participants.
Conrad V Fernandez, Chris Skedgel, Charles Weijer. CMAJ 2004
63
14

The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
214
14

Receiving a summary of the results of a trial: qualitative study of participants' views.
Mary Dixon-Woods, Clare Jackson, Kate C Windridge, Sara Kenyon. BMJ 2006
76
14

Communication of pharmacogenetic research results to HIV-infected treated patients: standpoints of professionals and patients.
Grégoire Moutel, Nathalie Duchange, François Raffi, Lama I Sharara, Ioannis Théodorou, Violaine Noël, Sandrine de Montgolfier, Ingrid Callies, François Bricaire, Christian Hervé,[...]. Eur J Hum Genet 2005
24
16

Ethics of future disclosure of individual risk information in a genetic cohort study: a survey of donor preferences.
Kenji Matsui, Reidar K Lie, Yoshikuni Kita, Hirotsugu Ueshima. J Epidemiol 2008
20
20

Return of "accurate" and "actionable" results: yes!
Bartha Maria Knoppers, Claude Laberge. Am J Bioeth 2009
18
22

Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
73
14



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
14

Public perspectives on returning genetics and genomics research results.
J O'Daniel, S B Haga. Public Health Genomics 2011
57
14

Researcher practices on returning genetic research results.
Christopher Heaney, Genevieve Tindall, Joe Lucas, Susanne B Haga. Genet Test Mol Biomarkers 2010
25
16

Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting.
Conrad V Fernandez, Caron Strahlendorf, Denise Avard, Bartha M Knoppers, Colleen O'Connell, Eric Bouffet, David Malkin, Nada Jabado, Kym Boycott, Poul H Sorensen. Genet Med 2013
36
14


False hopes and best data: consent to research and the therapeutic misconception.
P S Appelbaum, L H Roth, C W Lidz, P Benson, W Winslade. Hastings Cent Rep 1987
567
10


Views of American oncologists about the purposes of clinical trials.
Steven Joffe, Jane C Weeks. J Natl Cancer Inst 2002
70
10

Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
184
10

The return of research results to participants: pilot questionnaire of adolescents and parents of children with cancer.
C V Fernandez, D Santor, C Weijer, C Strahlendorf, A Moghrabi, R Pentz, J Gao, E Kodish. Pediatr Blood Cancer 2007
50
10

Providing research results to participants: attitudes and needs of adolescents and parents of children with cancer.
Conrad Vincent Fernandez, Jun Gao, Caron Strahlendorf, Albert Moghrabi, Rebecca Davis Pentz, Raymond Carlton Barfield, Justin Nathaniel Baker, Darcy Santor, Charles Weijer, Eric Kodish. J Clin Oncol 2009
58
10

Issues of consent and feedback in a genetic epidemiological study of women with breast cancer.
M P M Richards, M Ponder, P Pharoah, S Everest, J Mackay. J Med Ethics 2003
43
10



Offering results to research subjects: U.S. Institutional Review Board policy.
Christa Kozanczyn, Katie Collins, Conrad V Fernandez. Account Res 2007
18
16



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.