A citation-based method for searching scientific literature

Teddy D Warner, Carol J Weil, Christopher Andry, Howard B Degenholtz, Lisa Parker, Latarsha J Carithers, Michelle Feige, David Wendler, Rebecca D Pentz. J Empir Res Hum Res Ethics 2018
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Broad Consent for Research With Biological Samples: Workshop Conclusions.
Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M Fullerton, Hank Greely, Mats G Hansson, Sara Hull, Scott Kim,[...]. Am J Bioeth 2015
130
25

Biobanking past, present and future: responsibilities and benefits.
Yvonne G De Souza, John S Greenspan. AIDS 2013
96
18

Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
37
18

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
79
18

Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
Laura M Beskow, Carrie B Dombeck, Cole P Thompson, J Kemp Watson-Ormond, Kevin P Weinfurt. Genet Med 2015
36
18

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
199
18

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
78
18

The moral concerns of biobank donors: the effect of non-welfare interests on willingness to donate.
Raymond G De Vries, Tom Tomlinson, H Myra Kim, Chris D Krenz, Kerry A Ryan, Nicole Lehpamer, Scott Y H Kim. Life Sci Soc Policy 2016
20
18



Research ethics. Paying patients for their tissue: the legacy of Henrietta Lacks.
Robert D Truog, Aaron S Kesselheim, Steven Joffe. Science 2012
21
12

Improving informed consent with minority participants: results from researcher and community surveys.
Sandra Crouse Quinn, Mary A Garza, James Butler, Craig S Fryer, Erica T Casper, Stephen B Thomas, David Barnard, Kevin H Kim. J Empir Res Hum Res Ethics 2012
14
14





The Mayo Clinic Biobank: a building block for individualized medicine.
Janet E Olson, Euijung Ryu, Kiley J Johnson, Barbara A Koenig, Karen J Maschke, Jody A Morrisette, Mark Liebow, Paul Y Takahashi, Zachary S Fredericksen, Ruchi G Sharma,[...]. Mayo Clin Proc 2013
129
12

Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
103
12

A qualitative study of participants' views on re-consent in a longitudinal biobank.
Mary Dixon-Woods, David Kocman, Liz Brewster, Janet Willars, Graeme Laurie, Carolyn Tarrant. BMC Med Ethics 2017
7
28

Cancer patient perceptions on the ethical and legal issues related to biobanking.
Zubin Master, Jaime O Claudio, Christen Rachul, Jean C Y Wang, Mark D Minden, Timothy Caulfield. BMC Med Genomics 2013
33
12

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
225
12

Biobanking 3.0: evidence based and customer focused biobanking.
Daniel Simeon-Dubach, Peter Watson. Clin Biochem 2014
61
12

Interactive multimedia consent for biobanking: a randomized trial.
Christian M Simon, David W Klein, Helen A Schartz. Genet Med 2016
23
12

Developing a simplified consent form for biobanking.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. PLoS One 2010
60
12

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
138
12

Potential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?
J L Ridgeway, L C Han, J E Olson, K A Lackore, B A Koenig, T J Beebe, J Y Ziegenfuss. Public Health Genomics 2013
27
12

Genes, cells, and biobanks: Yes, there's still a consent problem.
Timothy Caulfield, Blake Murdoch. PLoS Biol 2017
30
12

The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
David J Carey, Samantha N Fetterolf, F Daniel Davis, William A Faucett, H Lester Kirchner, Uyenlinh Mirshahi, Michael F Murray, Diane T Smelser, Glenn S Gerhard, David H Ledbetter. Genet Med 2016
142
12

Assessing the understanding of biobank participants.
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
102
12

Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
166
12

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
65
12

"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research.
Sandra S-J Lee, Mildred K Cho, Stephanie A Kraft, Nina Varsava, Katie Gillespie, Kelly E Ormond, Benjamin S Wilfond, David Magnus. Genet Med 2019
21
12

Empirical assessment of whether moderate payments are undue or unjust inducements for participation in clinical trials.
Scott D Halpern, Jason H T Karlawish, David Casarett, Jesse A Berlin, David A Asch. Arch Intern Med 2004
111
6



Payment of clinical research subjects.
Christine Grady. J Clin Invest 2005
160
6




The case for compensation of tissue donors.
R Tavar, T F Murphy. Arch Intern Med 2001
3
33

The effects of cancer research participation on patient experience: a mixed-methods analysis.
L McGrath-Lone, H Ward, C Schoenborn, S Day. Eur J Cancer Care (Engl) 2016
8
12

Ownership and use of tissue specimens for research.
Rina Hakimian, David Korn. JAMA 2004
49
6


Inclusion of diverse populations in genomic research and health services: Genomix workshop report.
Savio S Mathew, Julian Barwell, Nasaim Khan, Ella Lynch, Michael Parker, Nadeem Qureshi. J Community Genet 2017
15
6

Improving the informed consent process for research subjects with low literacy: a systematic review.
Leonardo Tamariz, Ana Palacio, Mauricio Robert, Erin N Marcus. J Gen Intern Med 2013
74
6


Patients' perception of the informed consent process for neurooncology clinical trials.
Eva Knifed, Nir Lipsman, Warren Mason, Mark Bernstein. Neuro Oncol 2008
20
6


Community Perceptions of Biobanking Participation: A Qualitative Study among Mexican-Americans in Three Texas Cities.
Natalia I Heredia, Sarah Krasny, Larkin L Strong, Laura Von Hatten, Lynne Nguyen, Belinda M Reininger, Lorna H McNeill, María E Fernández. Public Health Genomics 2017
16
6

Barriers and Strategies to Participation in Tissue Research Among African-American Men.
Bettina F Drake, Danielle Boyd, Kimberly Carter, Sarah Gehlert, Vetta Sanders Thompson. J Cancer Educ 2017
10
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.