A citation-based method for searching scientific literature

Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity



The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat. Biotechnol. 2015
77
20

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
79
20

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N. Engl. J. Med. 2015
15

Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
20
15

Policy implications of big data in the health sector.
Effy Vayena, Joan Dzenowagis, John S Brownstein, Aziz Sheikh. Bull. World Health Organ. 2018
17
17

Defining digital medicine.
Eric Elenko, Lindsay Underwood, Daphne Zohar. Nat. Biotechnol. 2015
55
15

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
162
15


Ethics and Epistemology in Big Data Research.
Wendy Lipworth, Paul H Mason, Ian Kerridge, John P A Ioannidis. J Bioeth Inq 2017
14
14

Big data in biomedicine.
Fabricio F Costa. Drug Discov. Today 2014
58
10

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat. Rev. Genet. 2009
121
10

Finding the missing link for big biomedical data.
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
139
10

Precision medicine: opportunities, possibilities, and challenges for patients and providers.
Samantha A Adams, Carolyn Petersen. J Am Med Inform Assoc 2016
25
10

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
43
10

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
393
10


Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
21
10

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
92
10

Informed Consent and the Disclosure of Clinical Results to Research Participants.
Alessandro Blasimme, Celine Moret, Samia A Hurst, Effy Vayena. Am J Bioeth 2017
3
66

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
78
10

Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
36
10

Digital health: meeting the ethical and policy challenges.
Effy Vayena, Tobias Haeusermann, Afua Adjekum, Alessandro Blasimme. Swiss Med Wkly 2018
17
11

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
10

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
25
10

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
27
10

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
76
10

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
110
10

Ethical challenges of big data in public health.
Effy Vayena, Marcel Salathé, Lawrence C Madoff, John S Brownstein. PLoS Comput. Biol. 2015
79
10


What makes clinical research ethical?
E J Emanuel, D Wendler, C Grady. JAMA 2000
952
10


HIPAA and Protecting Health Information in the 21st Century.
I Glenn Cohen, Michelle M Mello. JAMA 2018
20
10

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
61
10

The Role of Participants in a Medical Information Commons.
Mary A Majumder, Juli M Bollinger, Angela G Villanueva, Patricia A Deverka, Barbara A Koenig. J Law Med Ethics 2019
6
33

Health data cooperatives - citizen empowerment.
E Hafen, D Kossmann, A Brand. Methods Inf Med 2014
41
10

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
24
10

How Should Health Data Be Used?
Bonnie Kaplan. Camb Q Healthc Ethics 2016
17
11

The Pathway to Patient Data Ownership and Better Health.
Katherine A Mikk, Harry A Sleeper, Eric J Topol. JAMA 2017
13
15

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
10


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
5

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
17
5


The ethics of biobanks.
Sven Ove Hansson. Camb Q Healthc Ethics 2004
9
11

Ethics and evidence based medicine.
I Kerridge, M Lowe, D Henry. BMJ 1998
64
5



Criminal Prohibition of Wrongful Re‑identification: Legal Solution or Minefield for Big Data?
Mark Phillips, Edward S Dove, Bartha M Knoppers. J Bioeth Inq 2017
8
12


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.