A citation-based method for searching scientific literature

Ann H Partridge, Eric P Winer. JAMA 2002
Times Cited: 120







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



Times Cited
  Times     Co-cited
Similarity


Informing study participants of research results: an ethical imperative.
Conrad V Fernandez, Eric Kodish, Charles Weijer. IRB 2003
133
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
51

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
69
44

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
38


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
54


Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
220
26

Considerations and costs of disclosing study findings to research participants.
Conrad V Fernandez, Chris Skedgel, Charles Weijer. CMAJ 2004
63
38

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
43

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
47


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
21

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
23

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
20

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
17

Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
72
22

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
14


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
57
22


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
24






Best laid plans for offering results go awry.
Lisa S Parker. Am J Bioeth 2006
23
43

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
10

Communicating clinical trial results to research participants.
E Ray Dorsey, Christopher A Beck, Mary Adams, Gary Chadwick, Elisabeth A de Blieck, Colleen McCallum, Leslie Briner, Lisa Deuel, Anthony Clarke, Rick Stewart,[...]. Arch Neurol 2008
21
42

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
129
9


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

Medicine. Reestablishing the researcher-patient compact.
Isaac S Kohane, Kenneth D Mandl, Patrick L Taylor, Ingrid A Holm, Daniel J Nigrin, Louis M Kunkel. Science 2007
100
8

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
463
8

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
8


Dissemination of results in community-based participatory research.
Peggy G Chen, Nitza Diaz, Georgina Lucas, Marjorie S Rosenthal. Am J Prev Med 2010
83
9

Informing participants of allocation to placebo at trial closure: postal survey.
Zelda Di Blasi, Ted J Kaptchuk, John Weinman, Jos Kleijnen. BMJ 2002
24
29

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
7

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
10


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
7

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
296
7

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
24

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
43

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

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
26

What makes clinical research ethical?
E J Emanuel, D Wendler, C Grady. JAMA 2000
6


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.