A citation-based method for searching scientific literature

A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
Times Cited: 171







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



Times Cited
  Times     Co-cited
Similarity


Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
136
34

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
174
27

DNA data sharing: research participants' perspectives.
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
75
28

Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.
J M Oliver, M J Slashinski, T Wang, P A Kelly, S G Hilsenbeck, A L McGuire. Public Health Genomics 2012
74
24

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
95
16

Biobanking for research: a survey of patient population attitudes and understanding.
Alanna Kulchak Rahm, Michelle Wrenn, Nikki M Carroll, Heather Spencer Feigelson. J Community Genet 2013
56
26


Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
115
12

To share or not to share: a randomized trial of consent for data sharing in genome research.
Amy L McGuire, Jill M Oliver, Melody J Slashinski, Jennifer L Graves, Tao Wang, P Adam Kelly, William Fisher, Ching C Lau, John Goss, Mehmet Okcu,[...]. Genet Med 2011
68
17


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
43
25




Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
54
18

Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
37
27

Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
128
10

Public preferences regarding informed consent models for participation in population-based genomic research.
Jodyn Platt, Juli Bollinger, Rachel Dvoskin, Sharon L R Kardia, David Kaufman. Genet Med 2014
54
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
85
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
159
9


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
105
9

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
475
9

Two large-scale surveys on community attitudes toward an opt-out biobank.
Kyle B Brothers, Daniel R Morrison, Ellen W Clayton. Am J Med Genet A 2011
51
17

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
105
9

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
46
19

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
91
9

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
221
9

Why do participants enroll in population biobank studies? A systematic literature review.
Hélène Nobile, Eric Vermeulen, Kristof Thys, Manuela M Bergmann, Pascal Borry. Expert Rev Mol Diagn 2013
34
26

Veterans' attitudes regarding a database for genomic research.
David Kaufman, Juli Murphy, Lori Erby, Kathy Hudson, Joan Scott. Genet Med 2009
35
22

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
105
8

Personal privacy, public benefits, and biobanks: a conjoint analysis of policy priorities and public perceptions.
Daryl Pullman, Holly Etchegary, Katherine Gallagher, Kathleen Hodgkinson, Montgomery Keough, David Morgan, Catherine Street. Genet Med 2012
35
22


Glad you asked: participants' opinions of re-consent for dbGap data submission.
Evette J Ludman, Stephanie M Fullerton, Leslie Spangler, Susan Brown Trinidad, Monica M Fujii, Gail P Jarvik, Eric B Larson, Wylie Burke. J Empir Res Hum Res Ethics 2010
82
9

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
141
8

Factors influencing public participation in biobanking.
Mamoun Ahram, Areej Othman, Manal Shahrouri, Ebtihal Mustafa. Eur J Hum Genet 2014
39
20

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
8

Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
138
7

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
35
20

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
54
12

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
35
20

Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health.
Daniel B Thiel, Tevah Platt, Jodyn Platt, Susan B King, Sharon L R Kardia. J Community Genet 2014
25
28

Community engagement in US biobanking: multiplicity of meaning and method.
K M Haldeman, R J Cadigan, A Davis, A Goldenberg, G E Henderson, D Lassiter, E Reavely. Public Health Genomics 2014
18
38

Patients' views on identifiability of samples and informed consent for genetic research.
Sara Chandros Hull, Richard R Sharp, Jeffrey R Botkin, Mark Brown, Mark Hughes, Jeremy Sugarman, Debra Schwinn, Pamela Sankar, Dragana Bolcic-Jankovic, Brian R Clarridge,[...]. Am J Bioeth 2008
81
8

Study newsletters, community and ethics advisory boards, and focus group discussions provide ongoing feedback for a large biobank.
Catherine A McCarty, Ann Garber, Jonathan C Reeser, Norman C Fost. Am J Med Genet A 2011
33
21

Formative research on perceptions of biobanking: what community members think.
John S Luque, Gwendolyn P Quinn, Francisco A Montel-Ishino, Mariana Arevalo, Shalanda A Bynum, Shalewa Noel-Thomas, Kristen J Wells, Clement K Gwede, Cathy D Meade. J Cancer Educ 2012
69
10

Understanding public reactions to commercialization of biobanks and use of biobank resources.
Dianne Nicol, Christine Critchley, Rebekah McWhirter, Tess Whitton. Soc Sci Med 2016
30
23

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
335
6


The role of race and trust in tissue/blood donation for genetic research.
Jada Bussey-Jones, Joanne Garrett, Gail Henderson, Mairead Moloney, Connie Blumenthal, Giselle Corbie-Smith. Genet Med 2010
80
7


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.