A citation-based method for searching scientific literature

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
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Dissemination of results in community-based participatory research.
Peggy G Chen, Nitza Diaz, Georgina Lucas, Marjorie S Rosenthal. Am J Prev Med 2010
84
62


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
56

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
56

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
56

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
50


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
50

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
50

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
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
43

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
43

Informing clinical trial participants about study results.
Ann H Partridge, Eric P Winer. JAMA 2002
120
43

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
43

Considerations and costs of disclosing study findings to research participants.
Conrad V Fernandez, Chris Skedgel, Charles Weijer. CMAJ 2004
63
37


Response to written feedback of clinical data within a longitudinal study: a qualitative study exploring the ethical implications.
Karen Lorimer, Cindy M Gray, Kate Hunt, Sally Wyke, Annie Anderson, Michaela Benzeval. BMC Med Res Methodol 2011
12
33

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
25



Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
25

Does dissemination extend beyond publication: a survey of a cross section of public funded research in the UK.
Paul M Wilson, Mark Petticrew, Michael W Calnan, Irwin Nazareth. Implement Sci 2010
36
25

Researchers' experiences with and perceptions of returning results to participants: Study protocol.
Pearl A McElfish, Rachel S Purvis, Christopher R Long. Contemp Clin Trials Commun 2018
7
57

Health researchers' experiences, perceptions and barriers related to sharing study results with participants.
Christopher R Long, Rachel S Purvis, Elizabeth Flood-Grady, Kim S Kimminau, Robert L Rhyne, Mark R Burge, M Kathryn Stewart, Amy J Jenkins, Laura P James, Pearl A McElfish. Health Res Policy Syst 2019
16
25


Recommendations for the return of research results to study participants and guardians: a report from the Children's Oncology Group.
Conrad V Fernandez, Kathleen Ruccione, Robert J Wells, Jay B Long, Wendy Pelletier, Mary C Hooke, Rebecca D Pentz, Robert B Noll, Justin N Baker, Maura O'Leary,[...]. J Clin Oncol 2012
19
18

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
18

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
18

Communication and dissemination strategies to facilitate the use of health-related evidence.
Lauren McCormack, Stacey Sheridan, Megan Lewis, Vanessa Boudewyns, Cathy L Melvin, Christine Kistler, Linda J Lux, Katherine Cullen, Kathleen N Lohr. Evid Rep Technol Assess (Full Rep) 2013
54
18

Designing for dissemination among public health researchers: findings from a national survey in the United States.
Ross C Brownson, Julie A Jacobs, Rachel G Tabak, Christine M Hoehner, Katherine A Stamatakis. Am J Public Health 2013
133
18

Revisiting the Quantitative-Qualitative Debate: Implications for Mixed-Methods Research.
Joanna E M Sale, Lynne H Lohfeld, Kevin Brazil. Qual Quant 2002
93
18

Health Research Funding Agencies' Policies, Recommendations, and Tools for Dissemination.
Pearl A McElfish, Rachel S Purvis, M Kathryn Stewart, Laura James, Karen H Kim Yeary, Christopher R Long. Prog Community Health Partnersh 2018
8
37

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
12

"They should take time": disclosure of clinical trial results as part of a social relationship.
Aline Sarradon-Eck, Juliette Sakoyan, Alice Desclaux, Julien Mancini, Dominique Genre, Claire Julian-Reynier. Soc Sci Med 2012
10
20

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
12


Feedback of research findings for vaccine trials: experiences from two malaria vaccine trials involving healthy children on the Kenyan Coast.
Caroline Gikonyo, Dorcas Kamuya, Bibi Mbete, Patricia Njuguna, Ally Olotu, Philip Bejon, Vicki Marsh, Sassy Molyneux. Dev World Bioeth 2013
9
22

Breast-feeding in South Korea: factors influencing its initiation and duration.
Woojin Chung, Hanjoong Kim, Chung-Mo Nam. Public Health Nutr 2008
26
12

Why is therapeutic misconception so prevalent?
Charles W Lidz, Karen Albert, Paul Appelbaum, Laura B Dunn, Eve Overton, Ekaterina Pivovarova. Camb Q Healthc Ethics 2015
34
12

What makes clinical research ethical?
E J Emanuel, D Wendler, C Grady. JAMA 2000
12

Clinical trials and medical care: defining the therapeutic misconception.
Gail E Henderson, Larry R Churchill, Arlene M Davis, Michele M Easter, Christine Grady, Steven Joffe, Nancy Kass, Nancy M P King, Charles W Lidz, Franklin G Miller,[...]. PLoS Med 2007
221
12

Whatever happened to qualitative description?
M Sandelowski. Res Nurs Health 2000
12

Patients' views on incidental findings from clinical exome sequencing.
Kristin E Clift, Colin M E Halverson, Alexander S Fiksdal, Ashok Kumbamu, Richard R Sharp, Jennifer B McCormick. Appl Transl Genom 2015
57
12

Health research participants are not receiving research results: a collaborative solution is needed.
Christopher R Long, M Kathryn Stewart, Pearl A McElfish. Trials 2017
16
12

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
6



Participants' preference for type of leaflet used to feed back the results of a randomised trial: a survey.
Stephen Brealey, Lazaros Andronis, Laura Dennis, Christine Atwell, Stirling Bryan, Simon Coulton, Helen Cox, Ben Cross, Fiona Fylan, Andrew Garratt,[...]. Trials 2010
5
20


The research-treatment distinction: a problematic approach for determining which activities should have ethical oversight.
Nancy E Kass, Ruth R Faden, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
155
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.