A citation-based method for searching scientific literature

Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity



Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
27
23

The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
94
19

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
14

Policy implications of big data in the health sector.
Effy Vayena, Joan Dzenowagis, John S Brownstein, Aziz Sheikh. Bull World Health Organ 2018
20
15

Informed Consent and the Disclosure of Clinical Results to Research Participants.
Alessandro Blasimme, Celine Moret, Samia A Hurst, Effy Vayena. Am J Bioeth 2017
4
75

Defining digital medicine.
Eric Elenko, Lindsay Underwood, Daphne Zohar. Nat Biotechnol 2015
65
14

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
177
14

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
93
14



Ethics and Epistemology in Big Data Research.
Wendy Lipworth, Paul H Mason, Ian Kerridge, John P A Ioannidis. J Bioeth Inq 2017
15
13

Big data in biomedicine.
Fabricio F Costa. Drug Discov Today 2014
69
9

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
125
9

Finding the missing link for big biomedical data.
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
148
9

Precision medicine: opportunities, possibilities, and challenges for patients and providers.
Samantha A Adams, Carolyn Petersen. J Am Med Inform Assoc 2016
26
9

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
47
9

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
420
9


Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
21
9

A systematic review of barriers to data sharing in public health.
Willem G van Panhuis, Proma Paul, Claudia Emerson, John Grefenstette, Richard Wilder, Abraham J Herbst, David Heymann, Donald S Burke. BMC Public Health 2014
107
9

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
82
9

Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
38
9

Digital health: meeting the ethical and policy challenges.
Effy Vayena, Tobias Haeusermann, Afua Adjekum, Alessandro Blasimme. Swiss Med Wkly 2018
22
9

From the principles of genomic data sharing to the practices of data access committees.
Mahsa Shabani, Bartha Maria Knoppers, Pascal Borry. EMBO Mol Med 2015
23
9

BBMRI-ERIC Directory: 515 Biobanks with Over 60 Million Biological Samples.
Petr Holub, Morris Swertz, Robert Reihs, David van Enckevort, Heimo Müller, Jan-Eric Litton. Biopreserv Biobank 2016
28
9

Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach.
Menno Mostert, Annelien L Bredenoord, Monique C I H Biesaart, Johannes J M van Delden. Eur J Hum Genet 2016
32
9

Genetic incidental findings: autonomy regained?
Effy Vayena, John Tasioulas. Genet Med 2013
17
11

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
80
9

Research led by participants: a new social contract for a new kind of research.
Effy Vayena, Roger Brownsword, Sarah Jane Edwards, Bastian Greshake, Jeffrey P Kahn, Navjoyt Ladher, Jonathan Montgomery, Daniel O'Connor, Onora O'Neill, Martin P Richards,[...]. J Med Ethics 2016
31
9

Genomic incidental findings: reducing the burden to be fair.
Velizara Anastasova, Alessandro Blasimme, Sophie Julia, Anne Cambon-Thomsen. Am J Bioeth 2013
11
18

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
118
9

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
80
9

Ethical challenges of big data in public health.
Effy Vayena, Marcel Salathé, Lawrence C Madoff, John S Brownstein. PLoS Comput Biol 2015
86
9


What makes clinical research ethical?
E J Emanuel, D Wendler, C Grady. JAMA 2000
991
9

HIPAA and Protecting Health Information in the 21st Century.
I Glenn Cohen, Michelle M Mello. JAMA 2018
26
9

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
69
9

Health data cooperatives - citizen empowerment.
E Hafen, D Kossmann, A Brand. Methods Inf Med 2014
42
9

Genetic testing, insurance discrimination and medical research: what the United States can learn from peer countries.
Jean-Christophe Bélisle-Pipon, Effy Vayena, Robert C Green, I Glenn Cohen. Nat Med 2019
12
16

Considerations for ethics review of big data health research: A scoping review.
Marcello Ienca, Agata Ferretti, Samia Hurst, Milo Puhan, Christian Lovis, Effy Vayena. PLoS One 2018
27
9

How Should Health Data Be Used?
Bonnie Kaplan. Camb Q Healthc Ethics 2016
19
10

The Pathway to Patient Data Ownership and Better Health.
Katherine A Mikk, Harry A Sleeper, Eric J Topol. JAMA 2017
17
11

Protecting Your Patients' Interests in the Era of Big Data, Artificial Intelligence, and Predictive Analytics.
Patricia Balthazar, Peter Harri, Adam Prater, Nabile M Safdar. J Am Coll Radiol 2018
25
9

PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation.
Andrea C Tricco, Erin Lillie, Wasifa Zarin, Kelly K O'Brien, Heather Colquhoun, Danielle Levac, David Moher, Micah D J Peters, Tanya Horsley, Laura Weeks,[...]. Ann Intern Med 2018
9


Evidence based medicine: what it is and what it isn't.
D L Sackett, W M Rosenberg, J A Gray, R B Haynes, W S Richardson. BMJ 1996
4

Inter- and intra-biobank networks: classification of biobanks.
Darren Shickle, Marcus Griffin, Karen El-Arifi. Pathobiology 2010
19
5

Monitoring ethical, legal, and social issues in developing population genetic databases.
Melissa A Austin, Sarah E Harding, Courtney E McElroy. Genet Med 2003
18
5



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.