A citation-based method for searching scientific literature

Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
Times Cited: 79







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



Times Cited
  Times     Co-cited
Similarity


Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.
Colleen M McBride, Sharon Hensley Alford, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2009
87
30


Putting science over supposition in the arena of personalized genomics.
Colleen M McBride, Sharon Hensley Alford, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Nat Genet 2008
67
19

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
347
16

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
288
15


Social networkers' attitudes toward direct-to-consumer personal genome testing.
Amy L McGuire, Christina M Diaz, Tao Wang, Susan G Hilsenbeck. Am J Bioeth 2009
152
13

Consumer perceptions of direct-to-consumer personalized genomic risk assessments.
Cinnamon S Bloss, Laura Ornowski, Elana Silver, Michele Cargill, Vance Vanier, Nicholas J Schork, Eric J Topol. Genet Med 2010
89
12

Consumers' use of web-based information and their decisions about multiplex genetic susceptibility testing.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Lawrence C Brody, Andreas D Baxevanis. J Med Internet Res 2010
47
21

Considerations for designing a prototype genetic test for use in translational research.
C H Wade, C M McBride, S L R Kardia, L C Brody. Public Health Genomics 2010
20
50

Patients' understanding of and responses to multiplex genetic susceptibility test results.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2012
86
12

Racial and ethnic variations in knowledge and attitudes about genetic testing.
Eleanor Singer, Toni Antonucci, John Van Hoewyk. Genet Test 2004
121
11


The association between race and attitudes about predictive genetic testing.
Nikki Peters, Abigail Rose, Katrina Armstrong. Cancer Epidemiol Biomarkers Prev 2004
90
11

Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours.
Theresa M Marteau, David P French, Simon J Griffin, A T Prevost, Stephen Sutton, Clare Watkinson, Sophie Attwood, Gareth J Hollands. Cochrane Database Syst Rev 2010
195
11

Racial and ethnic disparities in awareness of genetic testing for cancer risk.
José A Pagán, Dejun Su, Lifeng Li, Katrina Armstrong, David A Asch. Am J Prev Med 2009
68
13



Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
214
10

Disclosure of APOE genotype for risk of Alzheimer's disease.
Robert C Green, J Scott Roberts, L Adrienne Cupples, Norman R Relkin, Peter J Whitehouse, Tamsen Brown, Susan LaRusse Eckert, Melissa Butson, A Dessa Sadovnick, Kimberly A Quaid,[...]. N Engl J Med 2009
317
8


Consumers' views of direct-to-consumer genetic information.
Colleen M McBride, Christopher H Wade, Kimberly A Kaphingst. Annu Rev Genomics Hum Genet 2010
55
12

Letting the genome out of the bottle--will we get our wish?
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N Engl J Med 2008
260
7


Genetic testing: psychological aspects and implications.
Caryn Lerman, Robert T Croyle, Kenneth P Tercyak, Heidi Hamann. J Consult Clin Psychol 2002
177
7

Future health applications of genomics: priorities for communication, behavioral, and social sciences research.
Colleen M McBride, Deborah Bowen, Lawrence C Brody, Celeste M Condit, Robert T Croyle, Marta Gwinn, Muin J Khoury, Laura M Koehly, Bruce R Korf, Theresa M Marteau,[...]. Am J Prev Med 2010
105
7

What can interest tell us about uptake of genetic testing? Intention and behavior amongst smokers related to patients with lung cancer.
S C Sanderson, S C O'Neill, L A Bastian, G Bepler, C M McBride. Public Health Genomics 2010
61
9

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
154
7

A systematic review of perceived risks, psychological and behavioral impacts of genetic testing.
Jodi T Heshka, Crystal Palleschi, Heather Howley, Brenda Wilson, Philip S Wells. Genet Med 2008
223
7

Warranted concerns, warranted outlooks: a focus group study of public understandings of genetic research.
Benjamin R Bates, John A Lynch, Jennifer L Bevan, Celeste M Condit. Soc Sci Med 2005
87
7

Effective recruitment and retention of minority research participants.
Antronette K Yancey, Alexander N Ortega, Shiriki K Kumanyika. Annu Rev Public Health 2006
657
7

Confronting genetic testing disparities: knowledge is power.
Michael Hall, Olufunmilayo I Olopade. JAMA 2005
64
9

Public knowledge of and attitudes toward genetics and genetic testing.
Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
134
7

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
7

The influence of health care policies and health care system distrust on willingness to undergo genetic testing.
Katrina Armstrong, Mary Putt, Chanita Hughes Halbert, David Grande, Jerome Sanford Schwartz, Kaijun Liao, Noora Marcus, Mirar Bristol Demeter, Judy Shea. Med Care 2012
31
19

Effects of racial and ethnic group and health literacy on responses to genomic risk information in a medically underserved population.
Kimberly A Kaphingst, Jewel D Stafford, Lucy D'Agostino McGowan, Joann Seo, Christina R Lachance, Melody S Goodman. Health Psychol 2015
24
25

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.
Muin J Khoury, Colleen M McBride, Sheri D Schully, John P A Ioannidis, W Gregory Feero, A Cecile J W Janssens, Marta Gwinn, Denise G Simons-Morton, Jay M Bernhardt, Michele Cargill,[...]. Genet Med 2009
152
6

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
6

Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.
Christina R Lachance, Lori A H Erby, Beth M Ford, Vincent C Allen, Kimberly A Kaphingst. Genet Med 2010
68
7


Direct-to-consumer genetic testing: good, bad or benign?
T Caulfield, N M Ries, P N Ray, C Shuman, B Wilson. Clin Genet 2010
51
9

Reasons for seeking genetic susceptibility testing among first-degree relatives of people with Alzheimer disease.
J Scott Roberts, Susan A LaRusse, Heather Katzen, Peter J Whitehouse, Melissa Barber, Stephen G Post, Norman Relkin, Kimberly Quaid, Robert H Pietrzak, L Adrienne Cupples,[...]. Alzheimer Dis Assoc Disord 2003
64
7

Differences between African Americans and Whites in their attitudes toward genetic testing for Alzheimer's disease.
Yvonne G Hipps, J Scott Roberts, Lindsay A Farrer, Robert C Green. Genet Test 2003
33
15

Health behavior changes after genetic risk assessment for Alzheimer disease: The REVEAL Study.
Serena Chao, J Scott Roberts, Theresa M Marteau, Rebecca Silliman, L Adrienne Cupples, Robert C Green. Alzheimer Dis Assoc Disord 2008
162
6

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.
S E Gollust, E S Gordon, C Zayac, G Griffin, M F Christman, R E Pyeritz, L Wawak, B A Bernhardt. Public Health Genomics 2012
112
6

Validation of screening questions for limited health literacy in a large VA outpatient population.
Lisa D Chew, Joan M Griffin, Melissa R Partin, Siamak Noorbaloochi, Joseph P Grill, Annamay Snyder, Katharine A Bradley, Sean M Nugent, Alisha D Baines, Michelle Vanryn. J Gen Intern Med 2008
801
6

Communicating genetic and genomic information: health literacy and numeracy considerations.
D H Lea, K A Kaphingst, D Bowen, I Lipkus, D W Hadley. Public Health Genomics 2011
142
6

Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing.
David J Kaufman, Juli M Bollinger, Rachel L Dvoskin, Joan A Scott. J Genet Couns 2012
114
6

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
6

Acceptance of genetic testing in a general population: age, education and gender differences.
A R Aro, A Hakonen, M Hietala, J Lönnqvist, P Niemelä, L Peltonen, P Aula. Patient Educ Couns 1997
52
9


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.