A citation-based method for searching scientific literature

Dave Wendler, Ezekiel Emanuel. Arch Intern Med 2002
Times Cited: 142







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



Times Cited
  Times     Co-cited
Similarity


Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
157
25

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
201
23

Research with stored biological samples: what do research participants want?
Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, Susan G Hilsenbeck, Franklin G Miller, Ezekiel J Emanuel, David Wendler. Arch Intern Med 2005
81
25

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
281
20

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
138
18

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
463
18

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
220
17


Research on stored biological samples: views of African American and White American cancer patients.
Rebecca D Pentz, Laurent Billot, David Wendler. Am J Med Genet A 2006
66
24

Informing study participants of research results: an ethical imperative.
Conrad V Fernandez, Eric Kodish, Charles Weijer. IRB 2003
133
16

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
229
15

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
195
15


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
296
14

Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
184
13

Consent to the use of stored DNA for genetics research: a survey of attitudes in the Jewish population.
M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
47
27


Assessing the understanding of biobank participants.
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
104
13


Consent for genetic research in a general population: the NHANES experience.
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
125
12




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
12

Prospective biorepository participants' perspectives on access to research results.
Laura M Beskow, Sondra J Smolek. J Empir Res Hum Res Ethics 2009
33
36

Informed consent for genetic research on stored tissue samples.
E W Clayton, K K Steinberg, M J Khoury, E Thomson, L Andrews, M J Kahn, L M Kopelman, J O Weiss. JAMA 1995
202
11

High rate of consent to bank biologic samples for future research: the Eastern Cooperative Oncology Group experience.
Thomas Malone, Paul J Catalano, Peter J O'Dwyer, Bruce Giantonio. J Natl Cancer Inst 2002
57
19

Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
97
11

Patients' views on identifiability of samples and informed consent for genetic research.
Sara Chandros Hull, Richard R Sharp, Jeffrey R Botkin, Mark Brown, Mark Hughes, Jeremy Sugarman, Debra Schwinn, Pamela Sankar, Dragana Bolcic-Jankovic, Brian R Clarridge,[...]. Am J Bioeth 2008
81
13

Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
157
10

Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
84
11

Trends in ethical and legal frameworks for the use of human biobanks.
A Cambon-Thomsen, E Rial-Sebbag, B M Knoppers. Eur Respir J 2007
155
10

Returning genetic research results to individuals: points-to-consider.
Gaile Renegar, Christopher J Webster, Steffen Stuerzebecher, Lea Harty, Susan E Ide, Beth Balkite, Taryn A Rogalski-Salter, Nadine Cohen, Brian B Spear, Diane M Barnes,[...]. Bioethics 2006
69
14

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
129
10

Disclosure of individual genetic data to research participants: the debate reconsidered.
Annelien L Bredenoord, Hester Y Kroes, Edwin Cuppen, Michael Parker, Johannes J M van Delden. Trends Genet 2011
149
10

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
10

Medicine. Reestablishing the researcher-patient compact.
Isaac S Kohane, Kenneth D Mandl, Patrick L Taylor, Ingrid A Holm, Daniel J Nigrin, Louis M Kunkel. Science 2007
100
9



Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
72
12

Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.
Ebony B Bookman, Aleisha A Langehorne, John H Eckfeldt, Kathleen C Glass, Gail P Jarvik, Michael Klag, Greg Koski, Arno Motulsky, Benjamin Wilfond, Teri A Manolio,[...]. Am J Med Genet A 2006
160
9

Duty to disclose what? Querying the putative obligation to return research results to participants.
F A Miller, R Christensen, M Giacomini, J S Robert. J Med Ethics 2008
90
10


Informing clinical trial participants about study results.
Ann H Partridge, Eric P Winer. JAMA 2002
120
9

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
9

The return of research results to participants: pilot questionnaire of adolescents and parents of children with cancer.
C V Fernandez, D Santor, C Weijer, C Strahlendorf, A Moghrabi, R Pentz, J Gao, E Kodish. Pediatr Blood Cancer 2007
50
16

The ethics of research using biobanks: reason to question the importance attributed to informed consent.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Arch Intern Med 2005
70
11

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
448
8


Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
114
8


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.