A citation-based method for searching scientific literature

Charles R Jonassaint, Eunice R Santos, Crystal M Glover, Perry W Payne, Grace-Ann Fasaye, Nefertiti Oji-Njideka, Stanley Hooker, Wenndy Hernandez, Morris W Foster, Rick A Kittles, Charmaine D Royal. Hum Genet 2010
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


Racial and ethnic variations in knowledge and attitudes about genetic testing.
Eleanor Singer, Toni Antonucci, John Van Hoewyk. Genet Test 2004
121
22

Identity and genetic ancestry tracing.
Carl Elliott, Paul Brodwin. BMJ 2002
24
18

Genetics. The illusive gold standard in genetic ancestry testing.
Sandra Soo-Jin Lee, Deborah A Bolnick, Troy Duster, Pilar Ossorio, Kimberly Tallbear. Science 2009
29
18



Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's disease.
Ibidapo Akinleye, J Scott Roberts, Charmaine D M Royal, Erin Linnenbringer, Thomas O Obisesan, Grace-Ann Fasaye, Robert C Green. J Genet Couns 2011
21
19

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
18

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
47
18

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
18


Genetics. The science and business of genetic ancestry testing.
Deborah A Bolnick, Duana Fullwiley, Troy Duster, Richard S Cooper, Joan H Fujimura, Jonathan Kahn, Jay S Kaufman, Jonathan Marks, Ann Morning, Alondra Nelson,[...]. Science 2007
71
13

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

Inferring genetic ancestry: opportunities, challenges, and implications.
Charmaine D Royal, John Novembre, Stephanie M Fullerton, David B Goldstein, Jeffrey C Long, Michael J Bamshad, Andrew G Clark. Am J Hum Genet 2010
96
13



Genetic ancestry and the search for personalized genetic histories.
Mark D Shriver, Rick A Kittles. Nat Rev Genet 2004
99
13

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
13


Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study.
Samantha A Streicher, Saskia C Sanderson, Ethylin Wang Jabs, Michael Diefenbach, Meg Smirnoff, Inga Peter, Carol R Horowitz, Barbara Brenner, Lynne D Richardson. J Community Genet 2011
59
13

Public interest and expectations concerning commercial genotyping and genetic risk assessment.
Oksana A Makeeva, Valentina V Markova, Valery P Puzyrev. Per Med 2009
15
20

Personal genomics and individual identities: motivations and moral imperatives of early users.
Michelle L McGowan, Jennifer R Fishman, Marcie A Lambrix. New Genet Soc 2010
69
13

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
13

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
13



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
65
13

Non-Darwinian estimation: my ancestors, my genes' ancestors.
Kenneth M Weiss, Jeffrey C Long. Genome Res 2009
45
9



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
9

Tilting at windmills no longer: a data-driven discussion of DTC DNA ancestry tests.
Jennifer K Wagner, Jill D Cooper, Rene Sterling, Charmaine D Royal. Genet Med 2012
22
9

What is 'public opinion' about genetics?
C Condit. Nat Rev Genet 2001
59
9

Blacks as me: narrative identity.
Francoise Baylis. Dev World Bioeth 2003
7
28

The legitimacy of genetic ancestry tests.
Tony Frudakis. Science 2008
7
28


Interpreting the implications of DNA ancestry tests.
Jennifer K Wagner. Perspect Biol Med 2010
7
28

Linkage of early-onset familial breast cancer to chromosome 17q21.
J M Hall, M K Lee, B Newman, J E Morrow, L A Anderson, B Huey, M C King. Science 1990
9

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
9

Low rates of acceptance of BRCA1 and BRCA2 test results among African American women at increased risk for hereditary breast-ovarian cancer.
Chanita Hughes Halbert, Lisa Kessler, Jill E Stopfer, Susan Domchek, E Paul Wileyto. Genet Med 2006
51
9

An agenda for personalized medicine.
Pauline C Ng, Sarah S Murray, Samuel Levy, J Craig Venter. Nature 2009
195
9

Interventions to improve risk communication in clinical genetics: systematic review.
A Edwards, J Gray, A Clarke, J Dundon, G Elwyn, C Gaff, K Hood, R Iredale, S Sivell, C Shaw,[...]. Patient Educ Couns 2008
76
9


Psychosocial impact of the lack of information given at referral about familial risk for cancer.
Alison Metcalfe, Julie Werrett, Lucy Burgess, Collette Clifford. Psychooncology 2007
20
10


Attitudes on DNA ancestry tests.
Jennifer K Wagner, Kenneth M Weiss. Hum Genet 2012
12
16

The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur J Hum Genet 2006
196
9

Client perceptions of the impact of genetic counseling: an exploratory study.
Patricia McCarthy Veach, Sarah E Truesdell, Bonnie S LeRoy, Dianne M Bartels. J Genet Couns 1999
34
9

Goals of genetic counseling.
B B Biesecker. Clin Genet 2001
119
9

Attitudes to prenatal diagnosis and termination of pregnancy for 30 conditions among women in Saudi Arabia and the UK.
Ayman Alsulaiman, Jenny Hewison, Khaled K Abu-Amero, Shenaz Ahmed, Josephine M Green, Janet Hirst. Prenat Diagn 2012
19
10

Assessment of the content and process of genetic counseling: a critical review of empirical studies.
Bettina Meiser, Jennifer Irle, Elizabeth Lobb, Kristine Barlow-Stewart. J Genet Couns 2008
97
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.