A citation-based method for searching scientific literature

Sarah B Garrett, Marie Murphy, James Wiley, Daniel Dohan. J Empir Res Hum Res Ethics 2017
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Interactive multimedia consent for biobanking: a randomized trial.
Christian M Simon, David W Klein, Helen A Schartz. Genet Med 2016
29
40


Design Issues in E-Consent.
John Wilbanks. J Law Med Ethics 2018
25
40

"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
36
40

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
87
40

Readability standards for informed-consent forms as compared with actual readability.
Michael K Paasche-Orlow, Holly A Taylor, Frederick L Brancati. N Engl J Med 2003
386
30

Perspectives on Electronic Informed Consent From Patients Underrepresented in Research in the United States: A Focus Group Study.
Christian M Simon, Helen A Schartz, Gary E Rosenthal, Eric L Eisenstein, David W Klein. J Empir Res Hum Res Ethics 2018
15
30

Participants' Understanding of Informed Consent for Biobanking: A Systematic Review.
Elizabeth R Eisenhauer, Alan R Tait, Soo Young Rieh, Cynthia M Arslanian-Engoren. Clin Nurs Res 2019
17
30

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
104
30

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
41
30



Incorporating Biobank Consent into a Healthcare Setting: Challenges for Patient Understanding.
T J Kasperbauer, Karen K Schmidt, Ariane Thomas, Susan M Perkins, Peter H Schwartz. AJOB Empir Bioeth 2021
5
60

Research consent forms: continued unreadability and increasing length.
M E LoVerde, A V Prochazka, R L Byyny. J Gen Intern Med 1989
58
20

Simplifying informed consent for biorepositories: stakeholder perspectives.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. Genet Med 2010
37
20

Decisional capacity for informed consent in schizophrenia research.
W T Carpenter, J M Gold, A C Lahti, C A Queern, R R Conley, J J Bartko, J Kovnick, P S Appelbaum. Arch Gen Psychiatry 2000
339
20



Effects of two formats of informed consent on knowledge amongst persons with advanced HIV disease in a clinical trial of didanosine.
B Tindall, S Forde, M W Ross, D Goldstein, S Barker, D A Cooper. Patient Educ Couns 1994
29
20

The Deaconess Informed Consent Comprehension Test: an assessment tool for clinical research subjects.
C K Miller, D C O'Donnell, H R Searight, R A Barbarash. Pharmacotherapy 1996
75
20



Formative Evaluation of Participant Experience With Mobile eConsent in the App-Mediated Parkinson mPower Study: A Mixed Methods Study.
Megan Doerr, Amy Maguire Truong, Brian M Bot, John Wilbanks, Christine Suver, Lara M Mangravite. JMIR Mhealth Uhealth 2017
36
20

Consent Processes for Mobile App Mediated Research: Systematic Review.
Sarah Moore, Anne-Marie Tassé, Adrian Thorogood, Ingrid Winship, Ma'n Zawati, Megan Doerr. JMIR Mhealth Uhealth 2017
20
20

Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research.
Amy Corneli, Emily Namey, Monique P Mueller, Jenae Tharaldson, Steve Sortijas, Thomas Grey, Jeremy Sugarman. J Empir Res Hum Res Ethics 2017
17
20

Clinical Trial Participants' Views of the Risks and Benefits of Data Sharing.
Michelle M Mello, Van Lieou, Steven N Goodman. N Engl J Med 2018
80
20

Patient Perspectives About Decisions to Share Medical Data and Biospecimens for Research.
Jihoon Kim, Hyeoneui Kim, Elizabeth Bell, Tyler Bath, Paulina Paul, Anh Pham, Xiaoqian Jiang, Kai Zheng, Lucila Ohno-Machado. JAMA Netw Open 2019
25
20

A systematic literature review of individuals' perspectives on privacy and genetic information in the United States.
Ellen W Clayton, Colin M Halverson, Nila A Sathe, Bradley A Malin. PLoS One 2018
43
20

Patient Preferences for Use of Archived Biospecimens from Oncology Trials When Adequacy of Informed Consent Is Unclear.
Jeffrey Peppercorn, Eric Campbell, Steve Isakoff, Nora K Horick, Julia Rabin, Katharine Quain, Lecia V Sequist, Aditya Bardia, Deborah Collyar, Fay Hlubocky,[...]. Oncologist 2020
4
50

Development of the Precision Link Biobank at Boston Children's Hospital: Challenges and Opportunities.
Florence T Bourgeois, Paul Avillach, Sek Won Kong, Michelle M Heinz, Tram A Tran, Ramkrishna Chakrabarty, Jonathan Bickel, Piotr Sliz, Erin M Borglund, Susan Kornetsky,[...]. J Pers Med 2017
13
20

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
276
20


Implementation of Electronic Consent at a Biobank: An Opportunity for Precision Medicine Research.
Natalie T Boutin, Kathleen Mathieu, Alison G Hoffnagle, Nicole L Allen, Victor M Castro, Megan Morash, P Pearl O'Rourke, Elizabeth L Hohmann, Neil Herring, Lynn Bry,[...]. J Pers Med 2016
34
20

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
179
20

Challenges in creating an opt-in biobank with a registrar-based consent process and a commercial EHR.
Keith Marsolo, Jeremy Corsmo, Michael G Barnes, Carrie Pollick, Jamie Chalfin, Jeremy Nix, Christopher Smith, Rajesh Ganta. J Am Med Inform Assoc 2012
19
20

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
173
20

Principles of human subjects protections applied in an opt-out, de-identified biobank.
Jill Pulley, Ellen Clayton, Gordon R Bernard, Dan M Roden, Daniel R Masys. Clin Transl Sci 2010
148
20

Moving From Understanding of Consent Conditions to Heuristics of Trust.
Michael M Burgess, Kieran C O'Doherty. Am J Bioeth 2019
6
33

Randomization to standard and concise informed consent forms: development of evidence-based consent practices.
Mary E Enama, Zonghui Hu, Ingelise Gordon, Pamela Costner, Julie E Ledgerwood, Christine Grady. Contemp Clin Trials 2012
31
20

Broad Consent for Research on Biospecimens: The Views of Actual Donors at Four U.S. Medical Centers.
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
23
20

Measuring Understanding and Respecting Trust in Biobank Consent.
T J Kasperbauer, Peter H Schwartz. Am J Bioeth 2019
4
50

Biobanks and the Moral Concerns of Donors: A Democratic Deliberation.
Raymond G De Vries, Kerry A Ryan, Linda Gordon, Chris D Krenz, Tom Tomlinson, Scott Jewell, Scott Y H Kim. Qual Health Res 2019
7
28

A review of the key issues associated with the commercialization of biobanks.
Timothy Caulfield, Sarah Burningham, Yann Joly, Zubin Master, Mahsa Shabani, Pascal Borry, Allan Becker, Michael Burgess, Kathryn Calder, Christine Critchley,[...]. J Law Biosci 2014
47
20

Encouraging Participation And Transparency In Biobank Research.
Kayte Spector-Bagdady, Raymond G De Vries, Michele G Gornick, Andrew G Shuman, Sharon Kardia, Jodyn Platt. Health Aff (Millwood) 2018
18
20

Saturation in qualitative research: exploring its conceptualization and operationalization.
Benjamin Saunders, Julius Sim, Tom Kingstone, Shula Baker, Jackie Waterfield, Bernadette Bartlam, Heather Burroughs, Clare Jinks. Qual Quant 2018
20

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance.
Wylie Burke, Laura M Beskow, Susan Brown Trinidad, Stephanie M Fullerton, Kathleen Brelsford. J Law Med Ethics 2018
12
20

Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data.
Maui Hudson, Nanibaa' A Garrison, Rogena Sterling, Nadine R Caron, Keolu Fox, Joseph Yracheta, Jane Anderson, Phil Wilcox, Laura Arbour, Alex Brown,[...]. Nat Rev Genet 2020
47
20


Informed consent conversations and documents: A quantitative comparison.
Shlomo A Koyfman, Chandana A Reddy, Sabahat Hizlan, Angela C Leek, And Eric D Kodish. Cancer 2016
21
10

Telephone-based nursing intervention improves the effectiveness of the informed consent process in cancer clinical trials.
N K Aaronson, E Visser-Pol, G H Leenhouts, M J Muller, A C van der Schot, F S van Dam, R B Keus, C C Koning, W W ten Bokkel Huinink, J A van Dongen,[...]. J Clin Oncol 1996
128
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.