A citation-based method for searching scientific literature

Catherine A McCarty, Anuradha Nair, Diane M Austin, Philip F Giampietro. Community Genet 2007
Times Cited: 61







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



Times Cited
  Times     Co-cited
Similarity


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
107
42

Development of a large-scale de-identified DNA biobank to enable personalized medicine.
D M Roden, J M Pulley, M A Basford, G R Bernard, E W Clayton, J R Balser, D R Masys. Clin Pharmacol Ther 2008
574
18

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
18

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
176
18


Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
86
16

Quality of informed consent in cancer clinical trials: a cross-sectional survey.
S Joffe, E F Cook, P D Cleary, J W Clark, J C Weeks. Lancet 2001
422
16

Marshfield Clinic Personalized Medicine Research Project (PMRP): design, methods and recruitment for a large population-based biobank.
Catherine A McCarty, Russell A Wilke, Philip F Giampietro, Steve D Wesbrook, Michael D Caldwell. Per Med 2005
143
14

Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project.
Catherine A McCarty, Donna Chapman-Stone, Teresa Derfus, Philip F Giampietro, Norman Fost. Am J Med Genet A 2008
62
14

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
13

Quality of informed consent: a new measure of understanding among research subjects.
S Joffe, E F Cook, P D Cleary, J W Clark, J C Weeks. J Natl Cancer Inst 2001
254
13

Beyond "misunderstanding": written information and decisions about taking part in a genetic epidemiology study.
Mary Dixon-Woods, Richard E Ashcroft, Clare J Jackson, Martin D Tobin, Joelle Kivits, Paul R Burton, Nilesh J Samani. Soc Sci Med 2007
87
13

Attitudes and perceptions of patients towards methods of establishing a DNA biobank.
Jill M Pulley, Margaret M Brace, Gordon R Bernard, Dan R Masys. Cell Tissue Bank 2008
75
11


Willingness to donate blood samples for genetic research: a survey from a community in Singapore.
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
57
12

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
98
11


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
182
11

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
Catherine A McCarty, Rex L Chisholm, Christopher G Chute, Iftikhar J Kullo, Gail P Jarvik, Eric B Larson, Rongling Li, Daniel R Masys, Marylyn D Ritchie, Dan M Roden,[...]. BMC Med Genomics 2011
461
11

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
138
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
461
9

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
9



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
9

Biobanking for research: a survey of patient population attitudes and understanding.
Alanna Kulchak Rahm, Michelle Wrenn, Nikki M Carroll, Heather Spencer Feigelson. J Community Genet 2013
59
10

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
9

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
8



Great expectations: views of genetic research participants regarding current and future genetic studies.
Gail Henderson, Joanne Garrett, Jada Bussey-Jones, Mairead Eastin Moloney, Connie Blumenthal, Giselle Corbie-Smith. Genet Med 2008
42
11

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
140
8

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
156
8

False hopes and best data: consent to research and the therapeutic misconception.
P S Appelbaum, L H Roth, C W Lidz, P Benson, W Winslade. Hastings Cent Rep 1987
571
8

DNA data sharing: research participants' perspectives.
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
77
8


PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Joshua C Denny, Marylyn D Ritchie, Melissa A Basford, Jill M Pulley, Lisa Bastarache, Kristin Brown-Gentry, Deede Wang, Dan R Masys, Dan M Roden, Dana C Crawford. Bioinformatics 2010
590
8

Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.
Marylyn D Ritchie, Joshua C Denny, Dana C Crawford, Andrea H Ramirez, Justin B Weiner, Jill M Pulley, Melissa A Basford, Kristin Brown-Gentry, Jeffrey R Balser, Daniel R Masys,[...]. Am J Hum Genet 2010
245
8

Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.
Joshua C Denny, Marylyn D Ritchie, Dana C Crawford, Jonathan S Schildcrout, Andrea H Ramirez, Jill M Pulley, Melissa A Basford, Daniel R Masys, Jonathan L Haines, Dan M Roden. Circulation 2010
98
8

Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
Abel N Kho, M Geoffrey Hayes, Laura Rasmussen-Torvik, Jennifer A Pacheco, William K Thompson, Loren L Armstrong, Joshua C Denny, Peggy L Peissig, Aaron W Miller, Wei-Qi Wei,[...]. J Am Med Inform Assoc 2012
190
8

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, W Andrew Faucett, Rongling Li, Teri A Manolio, Saskia C Sanderson, Joseph Kannry, Randi Zinberg, Melissa A Basford,[...]. Genet Med 2013
416
8

Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
Laura M Beskow, Carrie B Dombeck, Cole P Thompson, J Kemp Watson-Ormond, Kevin P Weinfurt. Genet Med 2015
42
11

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
8

Expanding the ethical analysis of biobanks.
Mark A Rothstein. J Law Med Ethics 2005
56
7

Implications of disclosing individual results of clinical research.
Ellen Wright Clayton, Lainie Friedman Ross. JAMA 2006
75
6

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
185
6

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
6

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
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.