A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
286
23

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
32
56

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
306
17

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
17

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
70
24

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
61
27

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
477
16

Informing clinical trial participants about study results.
Ann H Partridge, Eric P Winer. JAMA 2002
120
16

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
210
16

Informing study participants of research results: an ethical imperative.
Conrad V Fernandez, Eric Kodish, Charles Weijer. IRB 2003
134
16

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
78
19

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
34
44


Public perspectives on returning genetics and genomics research results.
J O'Daniel, S B Haga. Public Health Genomics 2011
59
22


Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
223
12

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
23

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
138
11

Considerations and costs of disclosing study findings to research participants.
Conrad V Fernandez, Chris Skedgel, Charles Weijer. CMAJ 2004
64
17

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
93
11

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
198
11

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
254
11

Dissemination of results in community-based participatory research.
Peggy G Chen, Nitza Diaz, Georgina Lucas, Marjorie S Rosenthal. Am J Prev Med 2010
92
11

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
163
10

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
24
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
65
13

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
162
9


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
19


Meeting the obligation to communicate clinical trial results to study volunteers.
Kenneth Getz, Zachary Hallinan, Diane Simmons, Marla Jo Brickman, Zhanna Jumadilova, Lynne Pauer, Marc Wilenzick, Briggs Morrison. Expert Rev Clin Pharmacol 2012
12
75

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
153
8


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
20
40

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
18
44

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

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
122
7

Researchers' views on return of incidental genomic research results: qualitative and quantitative findings.
Robert Klitzman, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung. Genet Med 2013
86
8


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
16
43

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
51
13


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
20
35

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
20
35

Providing the results of research to participants: a mixed-method study of the benefits and challenges of a consultative approach.
Mary Dixon-Woods, Carolyn Tarrant, Clare J Jackson, David R Jones, Sara Kenyon. Clin Trials 2011
14
42

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
51
11


Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
75
8

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
22
27

IRB perspectives on the return of individual results from genomic research.
Lynn G Dressler, Sondra Smolek, Roselle Ponsaran, Janell M Markey, Helene Starks, Nancy Gerson, Susan Lewis, Nancy Press, Eric Juengst, Georgia L Wiesner. Genet Med 2012
51
11


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.