A citation-based method for searching scientific literature

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
Times Cited: 69







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



Times Cited
  Times     Co-cited
Similarity



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
51
62

Informing clinical trial participants about study results.
Ann H Partridge, Eric P Winer. JAMA 2002
120
46

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
75
46

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
48

Informing study participants of research results: an ethical imperative.
Conrad V Fernandez, Eric Kodish, Charles Weijer. IRB 2003
133
40



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
54

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
51
47

Considerations and costs of disclosing study findings to research participants.
Conrad V Fernandez, Chris Skedgel, Charles Weijer. CMAJ 2004
63
33


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
34


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

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
21

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
29
44


Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
222
17

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
15


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
14

Dissemination of results in community-based participatory research.
Peggy G Chen, Nitza Diaz, Georgina Lucas, Marjorie S Rosenthal. Am J Prev Med 2010
84
14

Health research participants' preferences for receiving research results.
Christopher R Long, M Kathryn Stewart, Thomas V Cunningham, T Scott Warmack, Pearl A McElfish. Clin Trials 2016
26
38


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
56

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
57



Offering results to research participants.
S Danielle MacNeil, Conrad V Fernandez. BMJ 2006
20
40

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
203
11

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
14
57

Participants' uptake of clinical trial results: a randomised experiment.
J Mancini, D Genre, F Dalenc, J-M Ferrero, P Kerbrat, A-L Martin, H Roché, F Maylevin, C Tarpin, P Viens,[...]. Br J Cancer 2010
15
53

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

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
35


Community dissemination and genetic research: moving beyond results reporting.
Susan Brown Trinidad, Evette J Ludman, Scarlett Hopkins, Rosalina D James, Theresa J Hoeft, Annie Kinegak, Henry Lupie, Ralph Kinegak, Bert B Boyer, Wylie Burke. Am J Med Genet A 2015
18
38

Qualitative study of participants' perceptions and preferences regarding research dissemination.
Rachel S Purvis, Traci H Abraham, Christopher R Long, M Kathryn Stewart, T Scott Warmack, Pearl Anna McElfish. AJOB Empir Bioeth 2017
18
38

What makes clinical research ethical?
E J Emanuel, D Wendler, C Grady. JAMA 2000
8

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
13

Informing participants of allocation to placebo at trial closure: postal survey.
Zelda Di Blasi, Ted J Kaptchuk, John Weinman, Jos Kleijnen. BMJ 2002
24
25

Perception of quality of life before and after disclosure of trial results: a report from the Program on the Surgical Control of the Hyperlipidemias (POSCH).
H Buchwald, L L Fitch, J P Matts, J W Johnson, B J Hansen, M R Stuenkel, H B Brooks. Control Clin Trials 1993
17
35

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
8



Communicating the results of research: how do participants of a cardiac rehabilitation RCT prefer to be informed?
Hasnain Dalal, Jennifer Wingham, Colin Pritchard, Sharon Northey, Philip Evans, Rod S Taylor, John Campbell. Health Expect 2010
10
60

Offering results to research subjects: U.S. Institutional Review Board policy.
Christa Kozanczyn, Katie Collins, Conrad V Fernandez. Account Res 2007
18
27

Disclosure of genetics research results after the death of the patient participant: a qualitative study of the impact on relatives.
E Ormondroyd, C Moynihan, M Watson, C Foster, S Davolls, A Ardern-Jones, R Eeles. J Genet Couns 2007
32
15

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
20

Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
72
7


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.