A citation-based method for searching scientific literature

M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
Times Cited: 47







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



Times Cited
  Times     Co-cited
Similarity



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
48

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
44

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
34


High rate of consent to bank biologic samples for future research: the Eastern Cooperative Oncology Group experience.
Thomas Malone, Paul J Catalano, Peter J O'Dwyer, Bruce Giantonio. J Natl Cancer Inst 2002
57
25

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
75
25

Informed consent for genetic research on stored tissue samples.
E W Clayton, K K Steinberg, M J Khoury, E Thomson, L Andrews, M J Kahn, L M Kopelman, J O Weiss. JAMA 1995
202
23

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
140
23

Willingness to donate blood samples for genetic research: a survey from a community in Singapore.
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
57
23



Research on stored biological samples: views of African American and White American cancer patients.
Rebecca D Pentz, Laurent Billot, David Wendler. Am J Med Genet A 2006
65
17


Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
185
14


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
14

Attitudes of the Japanese public and doctors towards use of archived information and samples without informed consent: preliminary findings based on focus group interviews.
Atsushi Asai, Motoki Ohnishi, Etsuyo Nishigaki, Miho Sekimoto, Shunichi Fukuhara, Tsuguya Fukui. BMC Med Ethics 2002
24
25





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
210
12

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
182
12

DNA data sharing: research participants' perspectives.
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
77
12

Ethical issues in genetic research: disclosure and informed consent.
P R Reilly, M F Boshar, S H Holtzman. Nat Genet 1997
82
10


Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
56
10

Genetics. No longer de-identified.
Amy L McGuire, Richard A Gibbs. Science 2006
119
10

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
107
10

Racial differences in factors that influence the willingness to participate in medical research studies.
Vickie L Shavers, Charles F Lynch, Leon F Burmeister. Ann Epidemiol 2002
363
8

Patients' views on residual blood use for research purposes.
N Hamajima, K Tajima, H Oya, T Kato, K Okuma, H Kaneda, S Moritaka, T Kato. Jpn J Cancer Res 1998
10
40

Awareness and motivation of Japanese donors of blood for research.
T Nakayama, K Muto, N Yoshiike, T Yokoyama. Am J Public Health 1999
10
40

Racial differences in enrolment in a cancer genetics registry.
Patricia G Moorman, Celette Sugg Skinner, James P Evans, Beth Newman, James R Sorenson, Brian Calingaert, Lisa Susswein, T Sydnee Crankshaw, Cathrine Hoyo, Joellen M Schildkraut. Cancer Epidemiol Biomarkers Prev 2004
66
8



Patients' consent preferences for research uses of information in electronic medical records: interview and survey data.
Donald J Willison, Karim Keshavjee, Kalpana Nair, Charlie Goldsmith, Anne M Holbrook. BMJ 2003
87
8


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
71
8

Employees' perspectives on ethically important aspects of genetic research participation: a pilot study.
Laura Weiss Roberts, Teddy D Warner, Cynthia M A Geppert, Melinda Rogers, Katherine A Green Hammond. Compr Psychiatry 2005
17
23

Privacy in genetics research.
B P Fuller, M J Kahn, P A Barr, L Biesecker, E Crowley, J Garber, M K Mansoura, P Murphy, J Murray, J Phillips,[...]. Science 1999
51
8

Strategies for consulting with the community: the cases of four large-scale genetic databases.
B Godard, J Marshall, C Laberge, B M Knoppers. Sci Eng Ethics 2004
32
12

Trends in ethical and legal frameworks for the use of human biobanks.
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
158
8


Native Hawaiian preferences for informed consent and disclosure of results from genetic research.
Megan Fong, Kathryn L Braun, R Mei-Ling Chang. J Cancer Educ 2006
21
19


Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
86
8

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
176
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
163
8

Biobank Recruitment: Motivations for Nonparticipation.
Katrina A B Goddard, K Sabina Smith, Chuhe Chen, Carmit McMullen, Cheryl Johnson. Biopreserv Biobank 2009
29
13


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.