A citation-based method for searching scientific literature

Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Bioethics 2014
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


Informed choice in direct-to-consumer genetic testing (DTCGT) websites: a content analysis of benefits, risks, and limitations.
Amanda Singleton, Lori Hamby Erby, Kathryn V Foisie, Kimberly A Kaphingst. J Genet Couns 2012
41
30




A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
60
20

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
20


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
15

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
15




23andMe and the FDA.
George J Annas, Sherman Elias. N Engl J Med 2014
68
15


Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
214
15



Beyond clinical utility: The multiple values of DTC genetics.
Mauro Turrini, Barbara Prainsack. Appl Transl Genom 2016
20
15

Personal genome testing: do you know what you are buying?
Heidi C Howard, Pascal Borry. Am J Bioeth 2009
19
10

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
153
10

Generic consent for genetic screening.
S Elias, G J Annas. N Engl J Med 1994
114
10


Some limits of informed consent.
O O'Neill. J Med Ethics 2003
223
10



A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions.
A Cecile J W Janssens, Marta Gwinn, Linda A Bradley, Ben A Oostra, Cornelia M van Duijn, Muin J Khoury. Am J Hum Genet 2008
167
10

Perceptions of genetic counseling services in direct-to-consumer personal genomic testing.
B F Darst, L Madlensky, N J Schork, E J Topol, C S Bloss. Clin Genet 2013
23
10

Willingness-to-pay for predictive tests with no immediate treatment implications: a survey of US residents.
Peter J Neumann, Joshua T Cohen, James K Hammitt, Thomas W Concannon, Hannah R Auerbach, Chihui Fang, David M Kent. Health Econ 2012
87
10


Association between health-service use and multiplex genetic testing.
Robert J Reid, Colleen M McBride, Sharon Hensley Alford, Cristofer Price, Andreas D Baxevanis, Lawrence C Brody, Eric B Larson. Genet Med 2012
31
10

Nonpropositional content in direct-to-consumer genetic testing advertisements.
Pascal Borry, Mahsa Shabani, Heidi Carmen Howard. Am J Bioeth 2013
7
28


Direct-to-consumer genetic testing: reliable or risky?
David H Spencer, Christina Lockwood, Eric Topol, James P Evans, Robert C Green, Elizabeth Mansfield, Zivana Tezak. Clin Chem 2011
13
15

Personalized genomic medicine and the rhetoric of empowerment.
Eric T Juengst, Michael A Flatt, Richard A Settersten. Hastings Cent Rep 2012
37
10



Impact of direct-to-consumer genomic testing at long term follow-up.
Cinnamon S Bloss, Nathan E Wineinger, Burcu F Darst, Nicholas J Schork, Eric J Topol. J Med Genet 2013
104
10

Dealing with the unexpected: consumer responses to direct-access BRCA mutation testing.
Uta Francke, Cheri Dijamco, Amy K Kiefer, Nicholas Eriksson, Bianca Moiseff, Joyce Y Tung, Joanna L Mountain. PeerJ 2013
53
10

Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature.
Lesley Goldsmith, Leigh Jackson, Anita O'Connor, Heather Skirton. J Community Genet 2013
31
10

An epidemiological perspective on the future of direct-to-consumer personal genome testing.
A Cecile Jw Janssens, Cornelia M van Duijn. Investig Genet 2010
33
10

The promise of whole-exome sequencing in medical genetics.
Bahareh Rabbani, Mustafa Tekin, Nejat Mahdieh. J Hum Genet 2014
248
10

Customers or research participants? Guidance for research practices in commercialization of personal genomics.
Sara L Tobin, Mildred K Cho, Sandra S-J Lee, David C Magnus, Megan Allyse, Kelly E Ormond, Nanibaa' A Garrison. Genet Med 2012
10
20


Health system implications of direct-to-consumer personal genome testing.
Amy L McGuire, Wylie Burke. Public Health Genomics 2011
28
10


Ethical issues raised by whole genome sequencing.
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
32
10


Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
10

Direct-to-consumer genome scanning services. Also for children?
Pascal Borry, Heidi C Howard, Karine Sénécal, Denise Avard. Nat Rev Genet 2009
27
10



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.