A citation-based method for searching scientific literature

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
Times Cited: 73







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



Times Cited
  Times     Co-cited
Similarity


Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
551
19

"I don't want to be Henrietta Lacks": diverse patient perspectives on donating biospecimens for precision medicine research.
Sandra S-J Lee, Mildred K Cho, Stephanie A Kraft, Nina Varsava, Katie Gillespie, Kelly E Ormond, Benjamin S Wilfond, David Magnus. Genet Med 2019
27
44

Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
81
12

Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
86
10

Trust, Precision Medicine Research, and Equitable Participation of Underserved Populations.
Maya Sabatello, Shawneequa Callier, Nanibaa' A Garrison, Elizabeth G Cohn. Am J Bioeth 2018
9
88


A framework for enhancing ethical genomic research with Indigenous communities.
Katrina G Claw, Matthew Z Anderson, Rene L Begay, Krystal S Tsosie, Keolu Fox, Nanibaa' A Garrison. Nat Commun 2018
92
9

The Precision Medicine Nation.
Maya Sabatello, Paul S Appelbaum. Hastings Cent Rep 2017
18
33

Conducting Precision Medicine Research with African Americans.
Chanita Hughes Halbert, Jasmine McDonald, Susan Vadaparampil, LaShanta Rice, Melanie Jefferson. PLoS One 2016
26
23

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
87
8

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
8

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
81
8


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
169
6


From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
89
6

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
439
6



Increasing participation in genomic research and biobanking through community-based capacity building.
Elizabeth Gross Cohn, Maryam Husamudeen, Elaine L Larson, Janet K Williams. J Genet Couns 2015
22
18




Persons with disabilities as an unrecognized health disparity population.
Gloria L Krahn, Deborah Klein Walker, Rosaly Correa-De-Araujo. Am J Public Health 2015
247
5

The role of race and trust in tissue/blood donation for genetic research.
Jada Bussey-Jones, Joanne Garrett, Gail Henderson, Mairead Moloney, Connie Blumenthal, Giselle Corbie-Smith. Genet Med 2010
78
5

Disability inclusion in precision medicine research: a first national survey.
Maya Sabatello, Ying Chen, Yuan Zhang, Paul S Appelbaum. Genet Med 2019
11
36

Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative Study.
Karen Spencer, Caroline Sanders, Edgar A Whitley, David Lund, Jane Kaye, William Gregory Dixon. J Med Internet Res 2016
62
6

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
184
5

Biobanking: the foundation of personalized medicine.
Robert E Hewitt. Curr Opin Oncol 2011
161
5

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V Campbell, Calvin W L Ho, Kazuto Kato, Jusaku Minari, Chih-Hsing Ho, Colin Mitchell,[...]. BMC Med Ethics 2016
52
7

Patient and interest organizations' views on personalized medicine: a qualitative study.
Isabelle Budin-Ljøsne, Jennifer R Harris. BMC Med Ethics 2016
19
21

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
213
5

Reframing Consent for Clinical Research: A Function-Based Approach.
Neal W Dickert, Nir Eyal, Sara F Goldkind, Christine Grady, Steven Joffe, Bernard Lo, Franklin G Miller, Rebecca D Pentz, Robert Silbergleit, Kevin P Weinfurt,[...]. Am J Bioeth 2017
57
7


Biobanks and the Moral Concerns of Donors: A Democratic Deliberation.
Raymond G De Vries, Kerry A Ryan, Linda Gordon, Chris D Krenz, Tom Tomlinson, Scott Jewell, Scott Y H Kim. Qual Health Res 2019
5
80

Community engagement in US biobanking: multiplicity of meaning and method.
K M Haldeman, R J Cadigan, A Davis, A Goldenberg, G E Henderson, D Lassiter, E Reavely. Public Health Genomics 2014
16
18

An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
278
4

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
55
5

A solidarity-based approach to the governance of research biobanks.
Barbara Prainsack, Alena Buyx. Med Law Rev 2013
39
7


Engaging Māori in biobanking and genomic research: a model for biobanks to guide culturally informed governance, operational, and community engagement activities.
Angela Beaton, Maui Hudson, Moe Milne, Ramari Viola Port, Khyla Russell, Barry Smith, Valmaine Toki, Lynley Uerata, Phillip Wilcox, Karen Bartholomew,[...]. Genet Med 2017
31
9

Public and biobank participant attitudes toward genetic research participation and data sharing.
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
165
4

Two large-scale surveys on community attitudes toward an opt-out biobank.
Kyle B Brothers, Daniel R Morrison, Ellen W Clayton. Am J Med Genet A 2011
50
6

Metaphors matter: from biobank to a library of medical information.
Mildred K Cho, Nina Varsava, Stephanie A Kraft, Gary Ashwal, Katie Gillespie, David Magnus, Kelly E Ormond, Alex Thomas, Benjamin S Wilfond, Sandra S-J Lee. Genet Med 2018
5
60

Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.
Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017
12
25

Distributive justice, diversity, and inclusion in precision medicine: what will success look like?
Elizabeth G Cohn, Gail E Henderson, Paul S Appelbaum. Genet Med 2017
21
14

Genomics for the world.
Carlos D Bustamante, Esteban González Burchard, Francisco M De la Vega. Nature 2011
304
4

Public Health in the Precision-Medicine Era.
Ronald Bayer, Sandro Galea. N Engl J Med 2015
116
4

A Survey of U.S Adults' Opinions about Conduct of a Nationwide Precision Medicine Initiative® Cohort Study of Genes and Environment.
David J Kaufman, Rebecca Baker, Lauren C Milner, Stephanie Devaney, Kathy L Hudson. PLoS One 2016
51
5

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
4


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.