A citation-based method for searching scientific literature

C Molster, T Charles, A Samanek, P O'Leary. Public Health Genomics 2009
Times Cited: 82







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



Times Cited
  Times     Co-cited
Similarity


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
29

Public experiences, knowledge and expectations about medical genetics and the use of genetic information.
Lidewij Henneman, Danielle R M Timmermans, Gerrit van der Wal. Community Genet 2004
100
21


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
140
19


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
146
15




Age differences in genetic knowledge, health literacy and causal beliefs for health conditions.
S Ashida, M Goodman, C Pandya, L M Koehly, C Lachance, J Stafford, K A Kaphingst. Public Health Genomics 2011
65
15

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
10

The association between knowledge and attitudes about genetic testing for cancer risk in the United States.
Abigail Rose, Nikki Peters, Judy A Shea, Katrina Armstrong. J Health Commun 2005
50
18


Understandings of basic genetics in the United States: results from a national survey of black and white men and women.
K D Christensen, T E Jayaratne, J S Roberts, S L R Kardia, E M Petty. Public Health Genomics 2010
49
18

Lay understanding of familial risk of common chronic diseases: a systematic review and synthesis of qualitative research.
Fiona M Walter, Jon Emery, Dejana Braithwaite, Theresa M Marteau. Ann Fam Med 2004
180
9


Lay understanding of genetics: a test of a hypothesis.
M Richards, M Ponder. J Med Genet 1996
66
12

Development and evaluation of a genetics literacy assessment instrument for undergraduates.
Bethany Vice Bowling, Erin E Acra, Lihshing Wang, Melanie F Myers, Gary E Dean, Glenn C Markle, Christine L Moskalik, Carl A Huether. Genetics 2008
83
9

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
88
9

Effects of informed consent for individual genome sequencing on relevant knowledge.
K A Kaphingst, F M Facio, M-R Cheng, S Brooks, H Eidem, A Linn, B B Biesecker, L G Biesecker. Clin Genet 2012
83
9

Knowledge about genetics among African Americans.
Lisa Kessler, Aliya Collier, Chanita Hughes Halbert. J Genet Couns 2007
26
26


Attitude and knowledge about genetics and genetic testing.
H Etchegary, M Cappelli, B Potter, M Vloet, I Graham, M Walker, B Wilson. Public Health Genomics 2010
50
14

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
228
8


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
351
8

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
68
10

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
89
8


New literacy challenge for the twenty-first century: genetic knowledge is poor even among well educated.
Robert Chapman, Maxim Likhanov, Fatos Selita, Ilya Zakharov, Emily Smith-Woolley, Yulia Kovas. J Community Genet 2019
38
18

Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
215
7

The general public's information needs and perceptions regarding hereditary cancer: an application of the Integrated Change Model.
Hein de Vries, Ilse Mesters, Hermanna van de Steeg, Cora Honing. Patient Educ Couns 2005
164
7

What does "a gene for heart disease" mean? A focus group study of public understandings of genetic risk factors.
Benjamin R Bates, Alan Templeton, Paul J Achter, Tina M Harris, Celeste M Condit. Am J Med Genet A 2003
60
10

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
8

Public attitudes toward genetic testing: perceived benefits and objections.
Lidewij Henneman, Danielle R M Timmermans, Gerrit Van Der Wal. Genet Test 2006
50
12

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
7

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
117
7

Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010.
Lidewij Henneman, Eric Vermeulen, Carla G van El, Liesbeth Claassen, Danielle R M Timmermans, Martina C Cornel. Eur J Hum Genet 2013
72
8

A vision for the future of genomics research.
Francis S Collins, Eric D Green, Alan E Guttmacher, Mark S Guyer. Nature 2003
6





Racial and ethnic variations in knowledge and attitudes about genetic testing.
Eleanor Singer, Toni Antonucci, John Van Hoewyk. Genet Test 2004
127
6

Psychiatric genetic testing: attitudes and intentions among future users and providers.
Mett Marri Laegsgaard, Ole Mors. Am J Med Genet B Neuropsychiatr Genet 2008
32
15

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, Susannah Green, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2011
101
6

Relationship between public attitudes toward genomic studies related to medicine and their level of genomic literacy in Japan.
Izumi Ishiyama, Akiko Nagai, Kaori Muto, Akiko Tamakoshi, Minori Kokado, Kyoko Mimura, Tetsuro Tanzawa, Zentaro Yamagata. Am J Med Genet A 2008
33
15

Attitudes of patients with cancer about personalized medicine and somatic genetic testing.
Stacy W Gray, Katherine Hicks-Courant, Christopher S Lathan, Levi Garraway, Elyse R Park, Jane C Weeks. J Oncol Pract 2012
83
6

Consumers report lower confidence in their genetics knowledge following direct-to-consumer personal genomic testing.
Deanna Alexis Carere, Peter Kraft, Kimberly A Kaphingst, J Scott Roberts, Robert C Green. Genet Med 2016
41
12

Genetic essentialism: on the deceptive determinism of DNA.
Ilan Dar-Nimrod, Steven J Heine. Psychol Bull 2011
226
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.