A citation-based method for searching scientific literature

Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
Times Cited: 125







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



Times Cited
  Times     Co-cited
Similarity


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
136
21

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
62
30



Public attitudes towards preventive genomics and personal interest in genetic testing to prevent disease: a survey study.
Eric Vermeulen, Lidewij Henneman, Carla G van El, Martina C Cornel. Eur J Public Health 2014
34
38

Australian study on public knowledge of human genetics and health.
C Molster, T Charles, A Samanek, P O'Leary. Public Health Genomics 2009
75
16

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
79
15

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
97
11

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
138
11

Public attitudes and beliefs about genetics.
Celeste M Condit. Annu Rev Genomics Hum Genet 2010
52
19

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
55
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
43
20

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
228
9

Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review.
Katie E J Hann, Madeleine Freeman, Lindsay Fraser, Jo Waller, Saskia C Sanderson, Belinda Rahman, Lucy Side, Sue Gessler, Anne Lanceley. BMC Public Health 2017
80
11

Racial and ethnic variations in knowledge and attitudes about genetic testing.
Eleanor Singer, Toni Antonucci, John Van Hoewyk. Genet Test 2004
120
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
57
14

Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative.
Tara J Schmidlen, Laura Scheinfeldt, Ruixue Zhaoyang, Rachel Kasper, Kevin Sweet, Erynn S Gordon, Margaret Keller, Cathy Stack, Neda Gharani, Mary B Daly,[...]. J Genet Couns 2016
20
40


Public attitudes toward genetic testing: perceived benefits and objections.
Lidewij Henneman, Danielle R M Timmermans, Gerrit Van Der Wal. Genet Test 2006
48
16

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
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
108
7

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
40
17

Genetic literacy and patient perceptions of IBD testing utility and disease control: a randomized vignette study of genetic testing.
Gillian W Hooker, Holly Peay, Lori Erby, Theodore Bayless, Barbara B Biesecker, Debra L Roter. Inflamm Bowel Dis 2014
21
33

A survey of UK public interest in internet-based personal genome testing.
Lynn F Cherkas, Juliette M Harris, Elana Levinson, Tim D Spector, Barbara Prainsack. PLoS One 2010
75
9

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

How Well Do Customers of Direct-to-Consumer Personal Genomic Testing Services Comprehend Genetic Test Results? Findings from the Impact of Personal Genomics Study.
Jenny E Ostergren, Michele C Gornick, Deanna Alexis Carere, Sarah S Kalia, Wendy R Uhlmann, Mack T Ruffin, Joanna L Mountain, Robert C Green, J Scott Roberts. Public Health Genomics 2015
45
15

Measuring genetic knowledge: a brief survey instrument for adolescents and adults.
S M Fitzgerald-Butt, A Bodine, K M Fry, J Ash, A N Zaidi, V Garg, C A Gerhardt, K L McBride. Clin Genet 2016
16
43

Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
35
20

Health Orientation, Knowledge, and Attitudes toward Genetic Testing and Personalized Genomic Services: Preliminary Data from an Italian Sample.
Serena Oliveri, Marianna Masiero, Paola Arnaboldi, Ilaria Cutica, Chiara Fioretti, Gabriella Pravettoni. Biomed Res Int 2016
20
35



Genetic knowledge and attitudes of parents of children with congenital heart defects.
Sara M Fitzgerald-Butt, Jennifer Klima, Kelly Kelleher, Deena Chisolm, Kim L McBride. Am J Med Genet A 2014
12
50


Communicating genetic risk information for common disorders in the era of genomic medicine.
Denise M Lautenbach, Kurt D Christensen, Jeffrey A Sparks, Robert C Green. Annu Rev Genomics Hum Genet 2013
83
7

Genome-based health literacy: a new challenge for public health genomics.
E V Syurina, I Brankovic, N Probst-Hensch, A Brand. Public Health Genomics 2011
40
15


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
28
21

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
46
10

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
32
15


Understanding patient and provider perceptions and expectations of genomic medicine.
Michael J Hall, Andrea D Forman, Susan V Montgomery, Kim L Rainey, Mary B Daly. J Surg Oncol 2015
18
27

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
84
5

Parent and public interest in whole-genome sequencing.
Daniel S Dodson, Aaron J Goldenberg, Matthew M Davis, Dianne C Singer, Beth A Tarini. Public Health Genomics 2015
16
31

Direct-to-consumer personalized genomic testing.
Cinnamon S Bloss, Burcu F Darst, Eric J Topol, Nicholas J Schork. Hum Mol Genet 2011
60
8

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
354
5

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
5

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
83
6

Public awareness and use of direct-to-consumer personal genomic tests from four state population-based surveys, and implications for clinical and public health practice.
Katherine Kolor, Debra Duquette, Amy Zlot, Joan Foland, Beth Anderson, Rebecca Giles, Jennifer Wrathall, Muin J Khoury. Genet Med 2012
32
15

Young Adults' Belief in Genetic Determinism, and Knowledge and Attitudes towards Modern Genetics and Genomics: The PUGGS Questionnaire.
Rebecca Bruu Carver, Jérémy Castéra, Niklas Gericke, Neima Alice Menezes Evangelista, Charbel N El-Hani. PLoS One 2017
17
29


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.