A citation-based method for searching scientific literature

Benjamin R Bates, John A Lynch, Jennifer L Bevan, Celeste M Condit. Soc Sci Med 2005
Times Cited: 88







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



Times Cited
  Times     Co-cited
Similarity




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
710
13

Attitudes about genetics in underserved, culturally diverse populations.
Diana S Catz, Nancy S Green, Jonathan N Tobin, Michele A Lloyd-Puryear, Penny Kyler, Ann Umemoto, Jennifer Cernoch, Roxane Brown, Fredericka Wolman. Community Genet 2005
109
12

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
11


Mapping the human genome: an assessment of media coverage and public reaction.
Ellen S Tambor, Barbara A Bernhardt, Joann Rodgers, Neil A Holtzman, Gail Geller. Genet Med 2002
37
27



The association between race and attitudes about predictive genetic testing.
Nikki Peters, Abigail Rose, Katrina Armstrong. Cancer Epidemiol Biomarkers Prev 2004
95
9

Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.
Katrina Armstrong, Ellyn Micco, Amy Carney, Jill Stopfer, Mary Putt. JAMA 2005
301
9

Public knowledge and public trust.
Sarah Cunningham-Burley. Community Genet 2006
34
23

Racial and ethnic variations in knowledge and attitudes about genetic testing.
Eleanor Singer, Toni Antonucci, John Van Hoewyk. Genet Test 2004
127
7

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
10

Genetic research and health disparities.
Pamela Sankar, Mildred K Cho, Celeste M Condit, Linda M Hunt, Barbara Koenig, Patricia Marshall, Sandra Soo-Jin Lee, Paul Spicer. JAMA 2004
160
7

Informed lay preferences for delivery of racially varied pharmacogenomics.
Jennifer L Bevan, Jonh A Lynch, Tasha N Dubriwny, Tina M Harris, Paul J Achter, Amy L Reeder, Celeste M Condit. Genet Med 2003
47
12



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
6

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
6

Attitudes and misconceptions about predictive genetic testing for cancer risk.
Abigail L Rose, Nikki Peters, Judy A Shea, Katrina Armstrong. Community Genet 2005
34
17

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
7

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
79
7

Participation in genetic testing research varies by social group.
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
82
7

Exploring the public understanding of basic genetic concepts.
Angela D Lanie, Toby Epstein Jayaratne, Jane P Sheldon, Sharon L R Kardia, Elizabeth S Anderson, Merle Feldbaum, Elizabeth M Petty. J Genet Couns 2004
141
5

Exploration of the impact of messages about genes and race on lay attitudes.
C M Condit, R L Parrott, B R Bates, J Bevan, P J Achter. Clin Genet 2004
31
16

Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) study.
C Royal, A Baffoe-Bonnie, R Kittles, I Powell, J Bennett, G Hoke, C Pettaway, S Weinrich, S Vijayakumar, C Ahaghotu,[...]. Ann Epidemiol 2000
79
6


Attitudes of African American premedical students toward genetic testing and screening.
Sara L Laskey, Joseph Williams, Jacqui Pierre-Louis, MaryAnn O'Riordan, Anne Matthews, Nathaniel H Robin. Genet Med 2003
40
12

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
5

Great expectations: views of genetic research participants regarding current and future genetic studies.
Gail Henderson, Joanne Garrett, Jada Bussey-Jones, Mairead Eastin Moloney, Connie Blumenthal, Giselle Corbie-Smith. Genet Med 2008
42
11

The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues.
Stuart Hogarth, Gail Javitt, David Melzer. Annu Rev Genomics Hum Genet 2008
158
5

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
116
5

Intentions to participate in genetics research among African American smokers.
Chanita Hughes Halbert, Oscar H Gandy, Aliya Collier, Lee Shaker. Cancer Epidemiol Biomarkers Prev 2006
30
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
176
5

Effective recruitment and retention of minority research participants.
Antronette K Yancey, Alexander N Ortega, Shiriki K Kumanyika. Annu Rev Public Health 2006
680
5

Recruiting adolescents into genetic studies of smoking behavior.
Janet Audrain, Kenneth P Tercyak, Paula Goldman, Angelita Bush. Cancer Epidemiol Biomarkers Prev 2002
34
11

International perceptions and approval of gene therapy.
D R Macer, S Akiyama, A T Alora, Y Asada, J Azariah, H Azariah, M V Boost, P Chatwachirawong, Y Kato, V Kaushik. Hum Gene Ther 1995
34
11


The use of race variables in genetic studies of complex traits and the goal of reducing health disparities: a transdisciplinary perspective.
Alexandra E Shields, Michael Fortun, Evelynn M Hammonds, Patricia A King, Caryn Lerman, Rayna Rapp, Patrick F Sullivan. Am Psychol 2005
98
4

Barriers and strategies for sustained participation of African-American men in cohort studies.
Cathrine Hoyo, M LaVerne Reid, Paul A Godley, Theodore Parrish, Lenora Smith, Marilie Gammon. Ethn Dis 2003
24
16


Concerns over participation in genetic research among Malay-Muslims, Chinese and Indians in Singapore: a focus group study.
Mee Lian Wong, Kee Seng Chia, Sharon Wee, Sin Eng Chia, Jeannette Lee, Woon Puay Koh, Han Ming Shen, Julian Thumboo, Dicky Sofjan. Community Genet 2004
20
20

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
4

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
7

A legacy for the children--attitudes of older adults in the United Kingdom to genetic testing.
Heather Skirton, Lorraine Q Frazier, Amy O Calvin, Marlene Z Cohen. J Clin Nurs 2006
23
17

Ethnic differences in knowledge and attitudes about BRCA1 testing in women at increased risk.
C Hughes, A Gomez-Caminero, J Benkendorf, J Kerner, C Isaacs, J Barter, C Lerman. Patient Educ Couns 1997
163
4

Asking the right questions: views on genetic variation research among black and white research participants.
Jada Bussey-Jones, Gail Henderson, Joanne Garrett, Mairead Moloney, Connie Blumenthal, Giselle Corbie-Smith. J Gen Intern Med 2009
16
25



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.