A citation-based method for searching scientific literature

Conrad V Fernandez, Chris Skedgel, Charles Weijer. CMAJ 2004
Times Cited: 63







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



Times Cited
  Times     Co-cited
Similarity


Informing clinical trial participants about study results.
Ann H Partridge, Eric P Winer. JAMA 2002
120
42

Informing study participants of research results: an ethical imperative.
Conrad V Fernandez, Eric Kodish, Charles Weijer. IRB 2003
132
41


Do patients participating in clinical trials want to know study results?
Ann H Partridge, Harold J Burstein, Rebecca S Gelman, P Kelly Marcom, Eric P Winer. J Natl Cancer Inst 2003
64
36

Offering to return results to research participants: attitudes and needs of principal investigators in the Children's Oncology Group.
Conrad V Fernandez, Eric Kodish, Susan Shurin, Charles Weijer. J Pediatr Hematol Oncol 2003
46
50

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
220
36

Offering participants results of a clinical trial: sharing results of a negative study.
Ann H Partridge, Julia S Wong, Katherine Knudsen, Rebecca Gelman, Ebonie Sampson, Michele Gadd, Karyn L Bishop, Jay R Harris, Eric P Winer. Lancet 2005
68
33

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
160
33

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
33



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
74
28

Oncology physician and nurse practices and attitudes regarding offering clinical trial results to study participants.
Ann H Partridge, Nadia Hackett, Emily Blood, Rebecca Gelman, Steven Joffe, Susan Bauer-Wu, Katherine Knudsen, Karen Emmons, Deborah Collyar, Richard L Schilsky,[...]. J Natl Cancer Inst 2004
50
34

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
195
26

Impact on survivors of retinoblastoma when informed of study results on risk of second cancers.
Charlene J Schulz, Mary P Riddle, Heiddis B Valdimirsdottir, David H Abramson, Charles A Sklar. Med Pediatr Oncol 2003
50
32


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
30

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
22

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
56
23



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
201
17


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
15



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
15

Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
72
14

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
460
14



Disclosure of individual genetic data to research participants: the debate reconsidered.
Annelien L Bredenoord, Hester Y Kroes, Edwin Cuppen, Michael Parker, Johannes J M van Delden. Trends Genet 2011
149
11

Feedback of trial results to participants: a survey of clinicians' and patients' attitudes and experiences.
Karen Cox, Nima Moghaddam, Lydia Bird, Ruth Elkan. Eur J Oncol Nurs 2011
26
26

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
129
11


The rights of patients in research.
H Goodare, R Smith. BMJ 1995
88
9

Disclosure of research results to research participants: A pilot study of the needs and attitudes of adolescents and parents.
Conrad Vincent Fernandez, Shaureen Taweel, Eric D Kodish, Charles Weijer. Paediatr Child Health 2005
14
42

Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
138
9

Unblinding of trial participants to their treatment allocation: lessons from the Prospective Study of Pravastatin in the Elderly at Risk (PROSPER).
Eleanor M Dinnett, Moira M B Mungall, Jane A Kent, Elizabeth S Ronald, Karen E McIntyre, Elizabeth Anderson, Allan Gaw. Clin Trials 2005
20
30


Dissemination of research findings to research participants living with HIV in rural Uganda: challenges and rewards.
Anna Baylor, Conrad Muzoora, Mwebsa Bwana, Annet Kembabazi, Jessica E Haberer, Lynn T Matthews, Alexander C Tsai, Peter W Hunt, Jeffrey N Martin, David R Bangsberg. PLoS Med 2013
16
37

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
11

Obligations in offering to disclose genetic research results.
Conrad V Fernandez, Charles Weijer. Am J Bioeth 2006
28
17



The impact of sharing results of a randomized breast cancer clinical trial with study participants.
Ann H Partridge, A C Wolff, P K Marcom, P A Kaufman, L Zhang, R Gelman, C Moore, D Lake, G F Fleming, H S Rugo,[...]. Breast Cancer Res Treat 2009
13
38

Incidental findings in human subjects research: what do investigators owe research participants?
Franklin G Miller, Michelle M Mello, Steven Joffe. J Law Med Ethics 2008
70
7

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
7

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
157
7

Researcher perspectives on disclosure of incidental findings in genetic research.
Meredith C Meacham, Helene Starks, Wylie Burke, Kelly Edwards. J Empir Res Hum Res Ethics 2010
48
10


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.