A citation-based method for searching scientific literature

Michelle M Mello, Leslie E Wolf. N Engl J Med 2010
Times Cited: 198







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



Times Cited
  Times     Co-cited
Similarity


Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
626
14

Moving forward: breaking the cycle of mistrust between American Indians and researchers.
Christina M Pacheco, Sean M Daley, Travis Brown, Melissa Filippi, K Allen Greiner, Christine M Daley. Am J Public Health 2013
71
16


Broad Consent for Research With Biological Samples: Workshop Conclusions.
Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M Fullerton, Hank Greely, Mats G Hansson, Sara Hull, Scott Kim,[...]. Am J Bioeth 2015
146
10

Conducting research with tribal communities: sovereignty, ethics, and data-sharing issues.
Anna Harding, Barbara Harper, Dave Stone, Catherine O'Neill, Patricia Berger, Stuart Harris, Jamie Donatuto. Environ Health Perspect 2012
74
13

Alaska native people's perceptions, understandings, and expectations for research involving biological specimens.
Vanessa Y Hiratsuka, Jennifer K Brown, Theresa J Hoeft, Denise A Dillard. Int J Circumpolar Health 2012
36
27

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
481
9

Public preferences regarding informed consent models for participation in population-based genomic research.
Jodyn Platt, Juli Bollinger, Rachel Dvoskin, Sharon L R Kardia, David Kaufman. Genet Med 2014
55
14

Self-Determination in Health Research: An Alaska Native Example of Tribal Ownership and Research Regulation.
Vanessa Y Hiratsuka, Julie A Beans, Renee F Robinson, Jennifer L Shaw, Ileen Sylvester, Denise A Dillard. Int J Environ Res Public Health 2017
25
32

Exploring pathways to trust: a tribal perspective on data sharing.
Rosalina James, Rebecca Tsosie, Puneet Sahota, Myra Parker, Denise Dillard, Ileen Sylvester, John Lewis, Joseph Klejka, LeeAnna Muzquiz, Polly Olsen,[...]. Genet Med 2014
37
21

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
115
8

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.
Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V Pearson, Dietrich A Stephan, Stanley F Nelson, David W Craig. PLoS Genet 2008
460
7

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
232
7

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
7

Views of biobanking research among Alaska native people: the role of community context.
Vanessa Hiratsuka, Jennifer Brown, Denise Dillard. Prog Community Health Partnersh 2012
29
24

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
175
6


Bridging the divide between genomic science and indigenous peoples.
Bette Jacobs, Jason Roffenbender, Jeff Collmann, Kate Cherry, LeManuel Lee Bitsói, Kim Bassett, Charles H Evans. J Law Med Ethics 2010
28
21

Research ethics and indigenous communities.
Allyson Kelley, Annie Belcourt-Dittloff, Cheryl Belcourt, Gordon Belcourt. Am J Public Health 2013
38
15

American Indian health policy: historical trends and contemporary issues.
Donald Warne, Linda Bane Frizzell. Am J Public Health 2014
91
6

Creating research capacity through a tribally based institutional review board.
Deborah J Morton, Joely Proudfit, Daniel Calac, Martina Portillo, Geneva Lofton-Fitzsimmons, Theda Molina, Raymond Flores, Barbara Lawson-Risso, Romelle Majel-McCauley. Am J Public Health 2013
25
24

Misalliances in the Barrow Alcohol Study.
E F Foulks. Am Indian Alsk Native Ment Health Res 1989
45
13

Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
107
6

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
92
6

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
230
6

Risk, reward, and the double-edged sword: perspectives on pharmacogenetic research and clinical testing among Alaska Native people.
Jennifer L Shaw, Renee Robinson, Helene Starks, Wylie Burke, Denise A Dillard. Am J Public Health 2013
30
20

Genetic research in native communities.
Lorrieann Santos. Prog Community Health Partnersh 2008
32
15


Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
132
5

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
97
5

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
306
5

Research ethics. The complexities of genomic identifiability.
Laura L Rodriguez, Lisa D Brooks, Judith H Greenberg, Eric D Green. Science 2013
73
6

Tribal participatory research: mechanisms of a collaborative model.
Philip A Fisher, Thomas J Ball. Am J Community Psychol 2003
113
5

Lessons learned from community-based participatory research in Indian country.
Linda Burhansstipanov, Suzanne Christopher, Sister Ann Schumacher. Cancer Control 2005
113
5

Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
126
5


Review of community-based research: assessing partnership approaches to improve public health.
B A Israel, A J Schulz, E A Parker, A B Becker. Annu Rev Public Health 1998
5


Pharmacogenetic research in partnership with American Indian and Alaska Native communities.
Erica L Woodahl, Lawrence J Lesko, Scarlett Hopkins, Renee F Robinson, Kenneth E Thummel, Wylie Burke. Pharmacogenomics 2014
26
19




Perspectives on communication and engagement with regard to collecting biospecimens and family health histories for cancer research in a rural Alaska Native community.
Lisa G Dirks, Jennifer L Shaw, Vanessa Y Hiratsuka, Julie A Beans, Janet J Kelly, Denise A Dillard. J Community Genet 2019
9
55

"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
36
13

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
116
4

Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
137
4

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
55
7

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
107
4

Cancer patients' attitudes toward future research uses of stored human biological materials.
Paul R Helft, Victoria L Champion, Rachael Eckles, Cynthia S Johnson, Eric M Meslin. J Empir Res Hum Res Ethics 2007
40
10

Developing a simplified consent form for biobanking.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. PLoS One 2010
61
6


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.