A citation-based method for searching scientific literature

Oonagh Corrigan. Sociol Health Illn 2003
Times Cited: 164







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



Times Cited
  Times     Co-cited
Similarity


Refusing the information paradigm: informed consent, medical research, and patient participation.
Ulrike Felt, Milena D Bister, Michael Strassnig, Ursula Wagner. Health (London) 2009
29
34

Some limits of informed consent.
O O'Neill. J Med Ethics 2003
218
10

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
383
6





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
4

Informed consent in a changing environment.
Mary Boulton, Michael Parker. Soc Sci Med 2007
26
15

What makes clinical research in developing countries ethical? The benchmarks of ethical research.
Ezekiel J Emanuel, David Wendler, Jack Killen, Christine Grady. J Infect Dis 2004
436
4



Neuroscientists' everyday experiences of ethics: the interplay of regulatory, professional, personal and tangible ethical spheres.
Caragh Brosnan, Alan Cribb, Steven P Wainwright, Clare Williams. Sociol Health Illn 2013
10
40


Distrust, race, and research.
Giselle Corbie-Smith, Stephen B Thomas, Diane Marie M St George. Arch Intern Med 2002
637
4

Challenging assumptions about minority participation in US clinical research.
Jill A Fisher, Corey A Kalbaugh. Am J Public Health 2011
108
4



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
9

Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
122
4

Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials.
Adam Nishimura, Jantey Carey, Patricia J Erwin, Jon C Tilburt, M Hassan Murad, Jennifer B McCormick. BMC Med Ethics 2013
238
4

Participants' understanding of informed consent in clinical trials over three decades: systematic review and meta-analysis.
Nguyen Thanh Tam, Nguyen Tien Huy, Le Thi Bich Thoa, Nguyen Phuoc Long, Nguyen Thi Huyen Trang, Kenji Hirayama, Juntra Karbwang. Bull World Health Organ 2015
94
4



From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
217
3


Assessing decisional capacity for clinical research or treatment: a review of instruments.
Laura B Dunn, Milap A Nowrangi, Barton W Palmer, Dilip V Jeste, Elyn R Saks. Am J Psychiatry 2006
229
3

Quality of informed consent in cancer clinical trials: a cross-sectional survey.
S Joffe, E F Cook, P D Cleary, J W Clark, J C Weeks. Lancet 2001
419
3

Informed consent, anticipatory regulation and ethnographic practice.
Elizabeth Murphy, Robert Dingwall. Soc Sci Med 2007
47
6

Consent and assent to participate in research from people with dementia.
Susan Slaughter, Dixie Cole, Eileen Jennings, Marlene A Reimer. Nurs Ethics 2007
73
4


Judging the ethics of qualitative research: considering the "ethics as process" model.
P Ramcharan, J R Cutcliffe. Health Soc Care Community 2001
40
7

How sociology can save bioethics . . . maybe.
José López. Sociol Health Illn 2004
21
14




Clinical trials and medical care: defining the therapeutic misconception.
Gail E Henderson, Larry R Churchill, Arlene M Davis, Michele M Easter, Christine Grady, Steven Joffe, Nancy Kass, Nancy M P King, Charles W Lidz, Franklin G Miller,[...]. PLoS Med 2007
221
3

Are racial and ethnic minorities less willing to participate in health research?
David Wendler, Raynard Kington, Jennifer Madans, Gretchen Van Wye, Heidi Christ-Schmidt, Laura A Pratt, Otis W Brawley, Cary P Gross, Ezekiel Emanuel. PLoS Med 2006
491
3

Representation of the elderly, women, and minorities in heart failure clinical trials.
Asefeh Heiat, Cary P Gross, Harlan M Krumholz. Arch Intern Med 2002
483
3

Effective recruitment and retention of minority research participants.
Antronette K Yancey, Alexander N Ortega, Shiriki K Kumanyika. Annu Rev Public Health 2006
657
3

Participation in cancer clinical trials: race-, sex-, and age-based disparities.
Vivek H Murthy, Harlan M Krumholz, Cary P Gross. JAMA 2004
3

Informed consent for clinical trials: a comparative study of standard versus simplified forms.
T C Davis, R F Holcombe, H J Berkel, S Pramanik, S G Divers. J Natl Cancer Inst 1998
185
3

Informed consent for clinical trials: in search of the "best" method.
S J Edwards, R J Lilford, J Thornton, J Hewison. Soc Sci Med 1998
87
3



Proposing modesty for informed consent.
Michael M Burgess. Soc Sci Med 2007
22
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
3


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.