A citation-based method for searching scientific literature

Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
Times Cited: 125







List of co-cited articles
391 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
32


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
31


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
24



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
16

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
26


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
14


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
13


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
13

Factors associated with enrollment in cancer genetics research.
Beth M Ford, James S Evans, Elena M Stoffel, Judith Balmaña, Meredith M Regan, Sapna Syngal. Cancer Epidemiol Biomarkers Prev 2006
31
38

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
16


Consent to the use of stored DNA for genetics research: a survey of attitudes in the Jewish population.
M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
47
23

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
13

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
17


Obtaining informed consent for genetic studies: The multiethnic study of atherosclerosis.
David Green, Mary Cushman, Norma Dermond, Eric A Johnson, Cecilia Castro, Donna Arnett, Joel Hill, Teri A Manolio. Am J Epidemiol 2006
22
45

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
232
10

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
10

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
30

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
517
9

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
21

Consent for genetics studies among clinical trial participants: findings from Action for Health in Diabetes (Look AHEAD).
M A Espeland, K Dotson, S A Jaramillo, S E Kahn, B Harrison, M Montez, J P Foreyt, B Montgomery, W C Knowler. Clin Trials 2006
27
33

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
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
107
9

Distrust, race, and research.
Giselle Corbie-Smith, Stephen B Thomas, Diane Marie M St George. Arch Intern Med 2002
657
8



Consent for future genetic research: the NHANES experience in 2007-2008.
Geraldine M McQuillan, Kathryn S Porter. IRB 2011
11
72

Participation in cancer clinical trials: race-, sex-, and age-based disparities.
Vivek H Murthy, Harlan M Krumholz, Cary P Gross. JAMA 2004
7


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
9

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
7


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
7

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
10

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
11

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
138
7

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
7

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
6

Why are African Americans under-represented in medical research studies? Impediments to participation.
V L Shavers-Hornaday, C F Lynch, L F Burmeister, J C Torner. Ethn Health 1997
248
6

Factors that influence characteristics of genetic biobanks.
Jennifer E Sanner, Lorraine Frazier. J Nurs Scholarsh 2007
33
18


Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
137
6


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.