A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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

The path to personalized medicine.
Margaret A Hamburg, Francis S Collins. N Engl J Med 2010
947
7

Genomic medicine--a primer.
Alan E Guttmacher, Francis S Collins. N Engl J Med 2002
350
7



A vision for the future of genomics research.
Francis S Collins, Eric D Green, Alan E Guttmacher, Mark S Guyer. Nature 2003
997
6

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
335
6


The sequence of the human genome.
J C Venter, M D Adams, E W Myers, P W Li, R J Mural, G G Sutton, H O Smith, M Yandell, C A Evans, R A Holt,[...]. Science 2001
5

Research ethics. Research practice and participant preferences: the growing gulf.
S B Trinidad, S M Fullerton, E J Ludman, G P Jarvik, E B Larson, W Burke. Science 2011
67
7

Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and “personalized” medicine?
Wylie Burke, Hilary Burton, Alison E Hall, Mohamed Karmali, Muin J Khoury, Bartha Knoppers, Eric M Meslin, Fiona Stanley, Caroline F Wright, Ronald L Zimmern. Genet Med 2010
60
8

Finding the missing heritability of complex diseases.
Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti,[...]. Nature 2009
5

Will genetics revolutionize medicine?
N A Holtzman, T M Marteau. N Engl J Med 2000
255
5

Genomic medicine--an updated primer.
W Gregory Feero, Alan E Guttmacher, Francis S Collins. N Engl J Med 2010
280
5

First FDA authorization for next-generation sequencer.
Francis S Collins, Margaret A Hamburg. N Engl J Med 2013
121
5

Ten years on--the human genome and medicine.
Harold Varmus. N Engl J Med 2010
54
7


The ethical conduct of clinical research involving critically ill patients in the United States and Canada: principles and recommendations.
John M Luce, Deborah J Cook, Thomas R Martin, Derek C Angus, Homer A Boushey, J Randall Curtis, John E Heffner, Paul N Lanken, Mitchell M Levy, Paula Y Polite,[...]. Am J Respir Crit Care Med 2004
66
6

Research ethics and consent in the intensive care unit.
John M Luce. Curr Opin Crit Care 2003
25
16

Surrogate consent for research involving adults with impaired decision making: survey of Institutional Review Board practices.
Michelle Ng Gong, Gary Winkel, Rosamond Rhodes, Lynne D Richardson, Jeffrey H Silverstein. Crit Care Med 2010
26
15

Genomics. Deflating the genomic bubble.
James P Evans, Eric M Meslin, Theresa M Marteau, Timothy Caulfield. Science 2011
106
4

The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group.
Steven M Teutsch, Linda A Bradley, Glenn E Palomaki, James E Haddow, Margaret Piper, Ned Calonge, W David Dotson, Michael P Douglas, Alfred O Berg. Genet Med 2009
464
4

A map of human genome variation from population-scale sequencing.
Gonçalo R Abecasis, David Altshuler, Adam Auton, Lisa D Brooks, Richard M Durbin, Richard A Gibbs, Matt E Hurles, Gil A McVean. Nature 2010
4

Keeping pace with the times--the Genetic Information Nondiscrimination Act of 2008.
Kathy L Hudson, M K Holohan, Francis S Collins. N Engl J Med 2008
128
4

Clinical assessment incorporating a personal genome.
Euan A Ashley, Atul J Butte, Matthew T Wheeler, Rong Chen, Teri E Klein, Frederick E Dewey, Joel T Dudley, Kelly E Ormond, Aleksandra Pavlovic, Alexander A Morgan,[...]. Lancet 2010
462
4

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
4

Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
289
4

Welcome to the genomic era.
Alan E Guttmacher, Francis S Collins. N Engl J Med 2003
165
4

What Happens When Underperforming Big Ideas in Research Become Entrenched?
Michael J Joyner, Nigel Paneth, John P A Ioannidis. JAMA 2016
67
5

"Drivers" of translational cancer epidemiology in the 21st century: needs and opportunities.
Tram Kim Lam, Margaret Spitz, Sheri D Schully, Muin J Khoury. Cancer Epidemiol Biomarkers Prev 2013
36
11

Preemptive clinical pharmacogenetics implementation: current programs in five US medical centers.
Henry M Dunnenberger, Kristine R Crews, James M Hoffman, Kelly E Caudle, Ulrich Broeckel, Scott C Howard, Robert J Hunkler, Teri E Klein, William E Evans, Mary V Relling. Annu Rev Pharmacol Toxicol 2015
256
4

Genomics, Health Disparities, and Missed Opportunities for the Nation's Research Agenda.
Kathleen McGlone West, Erika Blacksher, Wylie Burke. JAMA 2017
40
10

The impact of communicating genetic risks of disease on risk-reducing health behaviour: systematic review with meta-analysis.
Gareth J Hollands, David P French, Simon J Griffin, A Toby Prevost, Stephen Sutton, Sarah King, Theresa M Marteau. BMJ 2016
231
4

Promises, promises, and precision medicine.
Michael J Joyner, Nigel Paneth. J Clin Invest 2019
46
8

Future health applications of genomics: priorities for communication, behavioral, and social sciences research.
Colleen M McBride, Deborah Bowen, Lawrence C Brody, Celeste M Condit, Robert T Croyle, Marta Gwinn, Muin J Khoury, Laura M Koehly, Bruce R Korf, Theresa M Marteau,[...]. Am J Prev Med 2010
102
3


Debating clinical utility.
Wylie Burke, A-M Laberge, N Press. Public Health Genomics 2010
46
6

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
3

Recommendations for informed consent forms for critical care clinical trials.
Henry J Silverman, John M Luce, Paul N Lanken, Alan H Morris, Andrea L Harabin, Cathryn F Oldmixon, B Taylor Thompson, Gordon R Bernard. Crit Care Med 2005
38
7

Stroke genetic research and adults with impaired decision-making capacity: a survey of IRB and investigator practices.
Donna T Chen, James F Meschia, Thomas G Brott, Robert D Brown, Bradford B Worrall. Stroke 2008
7
42

Considerations in the construction of an instrument to assess attitudes regarding critical illness gene variation research.
Bradley D Freeman, Carie R Kennedy, Dragana Bolcic-Jankovic, Alexander Eastman, Ellen Iverson, Erica Shehane, Aaron Celious, Jennifer Barillas, Brian Clarridge. J Empir Res Hum Res Ethics 2012
8
37

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
3

Ethical considerations in the collection of genetic data from critically ill patients: what do published studies reveal about potential directions for empirical ethics research?
B D Freeman, C R Kennedy, H L Frankel, B Clarridge, D Bolcic-Jankovic, E Iverson, E Shehane, A Celious, B A Zehnbauer, T G Buchman. Pharmacogenomics J 2010
8
37



Whole-genome sequencing for optimized patient management.
Matthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, Jennifer Friedman, Claudia Gonzaga-Jauregui, Irene Newsham, Jeffrey G Reid, John K Fink, Margaret B Morgan, Marie-Claude Gingras,[...]. Sci Transl Med 2011
177
3


Genomics for the world.
Carlos D Bustamante, Esteban González Burchard, Francisco M De la Vega. Nature 2011
300
3

Reconsidering the family history in primary care.
Eugene C Rich, Wylie Burke, Caryl J Heaton, Susanne Haga, Linda Pinsky, M Priscilla Short, Louise Acheson. J Gen Intern Med 2004
226
3

A formal risk-benefit framework for genomic tests: facilitating the appropriate translation of genomics into clinical practice.
David L Veenstra, Joshua A Roth, Louis P Garrison, Scott D Ramsey, Wylie Burke. Genet Med 2010
61
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.