A citation-based method for searching scientific literature

Klaus Hoeyer, Niels Lynöe. Med Health Care Philos 2006
Times Cited: 23







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



Times Cited
  Times     Co-cited
Similarity



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
26

The ethics of research using biobanks: reason to question the importance attributed to informed consent.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
70
17

False hopes and best data: consent to research and the therapeutic misconception.
P S Appelbaum, L H Roth, C W Lidz, P Benson, W Winslade. Hastings Cent Rep 1987
567
17

Empty ethics: the problem with informed consent.
Oonagh Corrigan. Sociol Health Illn 2003
164
17


Attitudes and perceptions of patients towards methods of establishing a DNA biobank.
Jill M Pulley, Margaret M Brace, Gordon R Bernard, Dan R Masys. Cell Tissue Bank 2008
74
17

Research understanding, attitude and awareness towards biobanking: a survey among Italian twin participants to a genetic epidemiological study.
Virgilia Toccaceli, Corrado Fagnani, Lorenza Nisticò, Cristina D'Ippolito, Lorenzo Giannantonio, Sonia Brescianini, Maria Antonietta Stazi. BMC Med Ethics 2009
19
21

Beyond "misunderstanding": written information and decisions about taking part in a genetic epidemiology study.
Mary Dixon-Woods, Richard E Ashcroft, Clare J Jackson, Martin D Tobin, Joelle Kivits, Paul R Burton, Nilesh J Samani. Soc Sci Med 2007
86
17

An investigation of patients' motivations for their participation in genetics-related research.
N Hallowell, S Cooke, G Crawford, A Lucassen, M Parker, C Snowdon. J Med Ethics 2010
69
17

Governing UK Biobank: the importance of ensuring public trust.
Richard Tutton, Jane Kaye, Klaus Hoeyer. Trends Biotechnol 2004
31
13

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
13

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
13

Consent for genetic research in a general population: the NHANES experience.
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
125
13


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
230
13

Attitudes and beliefs of African Americans toward participation in medical research.
G Corbie-Smith, S B Thomas, M V Williams, S Moody-Ayers. J Gen Intern Med 1999
695
13

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
217
13

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
13

"If I could in a small way help": motivations for and beliefs about sample donation for genetic research.
Marsha Michie, Gail Henderson, Joanne Garrett, Giselle Corbie-Smith. J Empir Res Hum Res Ethics 2011
26
13

Hypothetical and factual willingness to participate in biobank research.
Linus Johnsson, Gert Helgesson, Thorunn Rafnar, Ingibjorg Halldorsdottir, Kee-Seng Chia, Stefan Eriksson, Mats G Hansson. Eur J Hum Genet 2010
59
13

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
204
13



Tackling community concerns about commercialisation and genetic research: a modest interdisciplinary proposal.
Gillian Haddow, Graeme Laurie, Sarah Cunningham-Burley, Kathryn G Hunter. Soc Sci Med 2007
55
8


Why do women consent to surgery, even when they do not want to? An interactionist and Bourdieusian analysis.
Mary Dixon-Woods, Simon J Williams, Clare J Jackson, Andrea Akkad, Sara Kenyon, Marwan Habiba. Soc Sci Med 2006
41
8

Choosing embryos: ethical complexity and relational autonomy in staff accounts of PGD.
Kathryn Ehrich, Clare Williams, Bobbie Farsides, Jane Sandall, Rosamund Scott. Sociol Health Illn 2007
29
8


An empirical study of tissue banking in Australia: navigating regulatory and ethical challenges.
Georgina Clark, Wendy Lipworth, Bokey Les, J M Little, Ian H Kerridge. J Law Med 2006
4
50

Refusing the information paradigm: informed consent, medical research, and patient participation.
Ulrike Felt, Milena D Bister, Michael Strassnig, Ursula Wagner. Health (London) 2009
29
8


Dangerous intersections.
David Korn. Issues Sci Technol 1996
10
20

Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
98
8

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
8

Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study.
Linus Johnsson, Mats G Hansson, Stefan Eriksson, Gert Helgesson. BMJ 2008
45
8



Research with stored biological samples: what do research participants want?
Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, Susan G Hilsenbeck, Franklin G Miller, Ezekiel J Emanuel, David Wendler. Arch Intern Med 2005
81
8


Empirical data about women's attitudes towards a hypothetical pediatric biobank.
Alon B Neidich, Josh W Joseph, Carole Ober, Lainie Friedman Ross. Am J Med Genet A 2008
45
8


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
8

The therapeutic misconception: informed consent in psychiatric research.
P S Appelbaum, L H Roth, C Lidz. Int J Law Psychiatry 1982
378
8

Consent forms and the therapeutic misconception: the example of gene transfer research.
Nancy M P King, Gail E Henderson, Larry R Churchill, Arlene M Davis, Sara Chandros Hull, Daniel K Nelson, P Christy Parham-Vetter, Barbara Bluestone Rothschild, Michele M Easter, Benjamin S Wilfond. IRB 2005
56
8


Distrust, race, and research.
Giselle Corbie-Smith, Stephen B Thomas, Diane Marie M St George. Arch Intern Med 2002
637
8

Why do people cooperate with medical research? Findings from three studies.
Mary Dixon-Woods, Carolyn Tarrant. Soc Sci Med 2009
46
8




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.