A citation-based method for searching scientific literature

Cinnamon S Bloss, Burcu F Darst, Eric J Topol, Nicholas J Schork. Hum Mol Genet 2011
Times Cited: 61







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



Times Cited
  Times     Co-cited
Similarity


Demographic differences in the utilization of clinical and direct-to-consumer genetic testing.
Nikki M Carroll, Erica Blum-Barnett, Sarah D Madrid, Cabell Jonas, Kristen Janes, Monica Alvarado, Ruth Bedoy, Valerie Paolino, Nazneen Aziz, Elizabeth A McGlynn,[...]. J Genet Couns 2020
15
6



Diversity in Clinical and Biomedical Research: A Promise Yet to Be Fulfilled.
Sam S Oh, Joshua Galanter, Neeta Thakur, Maria Pino-Yanes, Nicolas E Barcelo, Marquitta J White, Danielle M de Bruin, Ruth M Greenblatt, Kirsten Bibbins-Domingo, Alan H B Wu,[...]. PLoS Med 2015
271
1


Racial and ethnic variations in knowledge and attitudes about genetic testing.
Eleanor Singer, Toni Antonucci, John Van Hoewyk. Genet Test 2004
127
1


Qualitative data analysis for health services research: developing taxonomy, themes, and theory.
Elizabeth H Bradley, Leslie A Curry, Kelly J Devers. Health Serv Res 2007
1

Return of Research-Related Genetic Test Results and Genetic Discrimination Concerns: Facilitators and Barriers of Genetic Research Participation in Diverse Groups.
Andrea N Burnett-Hartman, Erica Blum-Barnett, Nikki M Carroll, Sarah D Madrid, Cabell Jonas, Kristen Janes, Monica Alvarado, Ruth Bedoy, Valerie Paolino, Nazneen Aziz,[...]. Public Health Genomics 2020
9
11

Genetic Testing Awareness and Attitudes among Latinos: Exploring Shared Perceptions and Gender-Based Differences.
Jada G Hamilton, Elyse Shuk, Guedy Arniella, C Javier González, Geoffrey S Gold, Francesca Gany, Mark E Robson, Jennifer L Hay. Public Health Genomics 2016
29
3

Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease.
Yvonne Bombard, Elizabeth Penziner, Oksana Suchowersky, Mark Guttman, Jane S Paulsen, Joan L Bottorff, Michael R Hayden. Eur J Hum Genet 2008
39
2

Racial/Ethnic Disparities in Genomic Sequencing.
Daniel E Spratt, Tiffany Chan, Levi Waldron, Corey Speers, Felix Y Feng, Olorunseun O Ogunwobi, Joseph R Osborne. JAMA Oncol 2016
163
1

Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
141
1



Health IT, hacking, and cybersecurity: national trends in data breaches of protected health information.
Jay G Ronquillo, J Erik Winterholler, Kamil Cwikla, Raphael Szymanski, Christopher Levy. JAMIA Open 2018
18
5

Biobank Recruitment: Motivations for Nonparticipation.
Katrina A B Goddard, K Sabina Smith, Chuhe Chen, Carmit McMullen, Cheryl Johnson. Biopreserv Biobank 2009
30
3

Veterans' attitudes regarding a database for genomic research.
David Kaufman, Juli Murphy, Lori Erby, Kathy Hudson, Joan Scott. Genet Med 2009
38
2


De-identified genomic data sharing: the research participant perspective.
Deborah Goodman, Catherine O Johnson, Deborah Bowen, Megan Smith, Lari Wenzel, Karen Edwards. J Community Genet 2017
26
3

Attitudes toward genetic testing for cancer risk after genetic counseling and decision support: a qualitative comparison between hereditary cancer types.
Claire E Wakefield, Nadine A Kasparian, Bettina Meiser, Judi Homewood, Judy Kirk, Kathy Tucker. Genet Test 2007
9
11

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
163
1

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
210
1

Health research participants' preferences for receiving research results.
Christopher R Long, M Kathryn Stewart, Thomas V Cunningham, T Scott Warmack, Pearl A McElfish. Clin Trials 2016
36
2

Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur J Hum Genet 2016
62
1

Primary care patients' views and decisions about, experience of and reactions to direct-to-consumer genetic testing: a longitudinal study.
Katherine Wasson, Tonya Nashay Sanders, Nancy S Hogan, Sara Cherny, Kathy J Helzlsouer. J Community Genet 2013
25
4

Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
187
1

The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature.
Deborah Goodman, Deborah Bowen, Lari Wenzel, Paris Tehrani, Francis Fernando, Araksi Khacheryan, Farihah Chowdhury, Catherine O Johnson, Karen Edwards. Transl Behav Med 2018
17
5




Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results.
Robyn Hylind, Maureen Smith, Laura Rasmussen-Torvik, Sharon Aufox. J Community Genet 2018
14
7

A systematic literature review of individuals' perspectives on privacy and genetic information in the United States.
Ellen W Clayton, Colin M Halverson, Nila A Sathe, Bradley A Malin. PLoS One 2018
51
1

Formative research on perceptions of biobanking: what community members think.
John S Luque, Gwendolyn P Quinn, Francisco A Montel-Ishino, Mariana Arevalo, Shalanda A Bynum, Shalewa Noel-Thomas, Kristen J Wells, Clement K Gwede, Cathy D Meade. J Cancer Educ 2012
67
1

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
97
1

Preferences regarding genetic research results: comparing veterans and nonveterans responses.
N Arar, J Seo, S Lee, H E Abboud, L A Copeland, P Noel, M Parchman. Public Health Genomics 2010
16
6



Increasing the visibility of coding decisions in team-based qualitative research in nursing.
Carl Thompson, Dorothy McCaughan, Nicky Cullum, Trevor A Sheldon, Pauline Raynor. Int J Nurs Stud 2004
26
3


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.