A citation-based method for searching scientific literature

Rebekah E McWhirter, Christine R Critchley, Dianne Nicol, Don Chalmers, Tess Whitton, Margaret Otlowski, Michael M Burgess, Joanne L Dickinson. J Pers Med 2014
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
122
27

Enhancing citizen engagement in cancer screening through deliberative democracy.
Lucie Rychetnik, Stacy M Carter, Julia Abelson, Hazel Thornton, Alexandra Barratt, Vikki A Entwistle, Geraldine Mackenzie, Glenn Salkeld, Paul Glasziou. J Natl Cancer Inst 2013
36
27

Engaging the public on biobanks: outcomes of the BC biobank deliberation.
K C O'Doherty, M M Burgess. Public Health Genomics 2009
59
27


Effectiveness of public deliberation methods for gathering input on issues in healthcare: Results from a randomized trial.
Kristin L Carman, Coretta Mallery, Maureen Maurer, Grace Wang, Steve Garfinkel, Manshu Yang, Dierdre Gilmore, Amy Windham, Marjorie Ginsburg, Shoshanna Sofaer,[...]. Soc Sci Med 2015
28
22

From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
83
22

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
22

Assessing the public's views in research ethics controversies: deliberative democracy and bioethics as natural allies.
Scott Y H Kim, Ian F Wall, Aimee Stanczyk, Raymond De Vries. J Empir Res Hum Res Ethics 2009
40
22


Informed consent in biobank research: a deliberative approach to the debate.
David M Secko, Nina Preto, Simon Niemeyer, Michael M Burgess. Soc Sci Med 2009
79
22

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
161
16

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
122
16

Effect of public deliberation on attitudes toward surrogate consent for dementia research.
S Y H Kim, H M Kim, D S Knopman, R De Vries, L Damschroder, P S Appelbaum. Neurology 2011
17
17

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
151
16


Recruiting for representation in public deliberation on the ethics of biobanks.
Holly Longstaff, Michael M Burgess. Public Underst Sci 2010
26
16

Public and biobank participant attitudes toward genetic research participation and data sharing.
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
152
16

Deliberations about deliberative methods: issues in the design and evaluation of public participation processes.
Julia Abelson, Pierre-Gerlier Forest, John Eyles, Patricia Smith, Elisabeth Martin, Francois-Pierre Gauvin. Soc Sci Med 2003
269
16


Community engagement in biobanking: Experiences from the eMERGE Network.
Amy A Lemke, Joel T Wu, Carol Waudby, Jill Pulley, Carol P Somkin, Susan Brown Trinidad. Genom Soc Policy 2010
31
16


Genomic data in the electronic medical record: perspectives from a biobank community advisory board.
Brittany C Kimball, Katherine E Nowakowski, Karen J Maschke, Jennifer B McCormick. J Empir Res Hum Res Ethics 2014
17
11

Race and trust in the health care system.
L Ebony Boulware, Lisa A Cooper, Lloyd E Ratner, Thomas A LaVeist, Neil R Powe. Public Health Rep 2003
477
11

Stakeholder engagement: a key component of integrating genomic information into electronic health records.
Andrea Hartzler, Catherine A McCarty, Luke V Rasmussen, Marc S Williams, Murray Brilliant, Erica A Bowton, Ellen Wright Clayton, William A Faucett, Kadija Ferryman, Julie R Field,[...]. Genet Med 2013
37
11

EngageUC: Developing an Efficient and Ethical Approach to Biobanking Research at the University of California.
Sarah B Garrett, Barbara A Koenig, Arleen Brown, Jen R Hult, Elizabeth A Boyd, Sarah Dry, Daniel Dohan. Clin Transl Sci 2015
10
20



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
274
11

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
114
11

Researchers' views on informed consent for return of secondary results in genomic research.
Paul S Appelbaum, Abby Fyer, Robert L Klitzman, Josue Martinez, Erik Parens, Yuan Zhang, Wendy K Chung. Genet Med 2015
10
20

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur J Hum Genet 2016
100
11

Views of genetics health professionals on the return of genomic results.
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014
35
11

Reporting genomic secondary findings: ACMG members weigh in.
Maren T Scheuner, Jane Peredo, Judith Benkendorf, Bruce Bowdish, Gerald Feldman, Lynn Fleisher, John J Mulvihill, Michael Watson, Gail E Herman, James Evans. Genet Med 2015
33
11



Point-counterpoint. Ethics and genomic incidental findings.
Amy L McGuire, Steven Joffe, Barbara A Koenig, Barbara B Biesecker, Laurence B McCullough, Jennifer S Blumenthal-Barby, Timothy Caulfield, Sharon F Terry, Robert C Green. Science 2013
122
11


Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing.
Angela R Bradbury, Linda J Patrick-Miller, Brian L Egleston, Laura DiGiovanni, Jamie Brower, Diana Harris, Evelyn M Stevens, Kara N Maxwell, Abha Kulkarni, Tyler Chavez,[...]. Genet Med 2016
37
11


Realizing the promise of population biobanks: a new model for translation.
Madeleine J Murtagh, Ipek Demir, Jennifer R Harris, Paul R Burton. Hum Genet 2011
16
12

Predicting intention to biobank: a national survey.
Christine R Critchley, Dianne Nicol, Margaret F A Otlowski, Mark J A Stranger. Eur J Public Health 2012
36
11

Identifying public expectations of genetic biobanks.
Christine Critchley, Dianne Nicol, Rebekah McWhirter. Public Underst Sci 2017
15
13

Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
32
11

Citizens' Perspectives on Disinvestment from Publicly Funded Pathology Tests: A Deliberative Forum.
Jackie M Street, Peta Callaghan, Annette J Braunack-Mayer, Janet E Hiller. Value Health 2015
8
25


The use of citizens' juries in health policy decision-making: a systematic review.
Jackie Street, Katherine Duszynski, Stephanie Krawczyk, Annette Braunack-Mayer. Soc Sci Med 2014
74
11

Blueprint for a deliberative public forum on biobanking policy: were theoretical principles achievable in practice?
Caron Molster, Susannah Maxwell, Leanne Youngs, Gaenor Kyne, Fiona Hope, Hugh Dawkins, Peter O'Leary. Health Expect 2013
23
11


Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature.
Alma Husedzinovic, Dominik Ose, Christoph Schickhardt, Stefan Fröhling, Eva C Winkler. Eur J Hum Genet 2015
25
11

National survey and community advisory board development for a bipolar disorder biobank.
Mark A Frye, Allen Doederlein, Barbara Koenig, Susan L McElroy, Malik Nassan, Lisa R Seymour, Joanna M Biernacka, Allen S Daniels. Bipolar Disord 2015
7
28


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.