A citation-based method for searching scientific literature

Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
Times Cited: 29







List of co-cited articles
89 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
31
20


The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
110
17

Defining digital medicine.
Eric Elenko, Lindsay Underwood, Daphne Zohar. Nat Biotechnol 2015
69
13

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
208
13

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
10

Google DeepMind and healthcare in an age of algorithms.
Julia Powles, Hal Hodson. Health Technol (Berl) 2017
67
10

Policy implications of big data in the health sector.
Effy Vayena, Joan Dzenowagis, John S Brownstein, Aziz Sheikh. Bull World Health Organ 2018
27
11

Informed Consent and the Disclosure of Clinical Results to Research Participants.
Alessandro Blasimme, Celine Moret, Samia A Hurst, Effy Vayena. Am J Bioeth 2017
5
60

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
89
10

Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
43
10

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
110
10


Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
76
10

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
90
10

The other side of the coin: Harm due to the non-use of health-related data.
Kerina H Jones, Graeme Laurie, Leslie Stevens, Christine Dobbs, David V Ford, Nathan Lea. Int J Med Inform 2017
35
10

Public responses to the sharing and linkage of health data for research purposes: a systematic review and thematic synthesis of qualitative studies.
Mhairi Aitken, Jenna de St Jorre, Claudia Pagliari, Ruth Jepson, Sarah Cunningham-Burley. BMC Med Ethics 2016
89
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
78
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
38
10

Future-proofing biobanks' governance.
Felix Gille, Effy Vayena, Alessandro Blasimme. Eur J Hum Genet 2020
7
42

Ethics and Epistemology in Big Data Research.
Wendy Lipworth, Paul H Mason, Ian Kerridge, John P A Ioannidis. J Bioeth Inq 2017
17
11


Big data in biomedicine.
Fabricio F Costa. Drug Discov Today 2014
76
6

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
142
6

Finding the missing link for big biomedical data.
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
164
6

Precision medicine: opportunities, possibilities, and challenges for patients and providers.
Samantha A Adams, Carolyn Petersen. J Am Med Inform Assoc 2016
29
6

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
51
6

The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
122
6

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
463
6


Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
23
8

From public health genomics to precision public health: a 20-year journey.
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
50
6

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
120
6

Digital health: meeting the ethical and policy challenges.
Effy Vayena, Tobias Haeusermann, Afua Adjekum, Alessandro Blasimme. Swiss Med Wkly 2018
25
8


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
24
8

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
34
6


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
34
6

Redefining genomic privacy: trust and empowerment.
Yaniv Erlich, James B Williams, David Glazer, Kenneth Yocum, Nita Farahany, Maynard Olson, Arvind Narayanan, Lincoln D Stein, Jan A Witkowski, Robert C Kain. PLoS Biol 2014
50
6

Big Data in Public Health: Terminology, Machine Learning, and Privacy.
Stephen J Mooney, Vikas Pejaver. Annu Rev Public Health 2018
55
6

Privacy Challenges of Genomic Big Data.
Hong Shen, Jian Ma. Adv Exp Med Biol 2017
7
28




Genetic incidental findings: autonomy regained?
Effy Vayena, John Tasioulas. Genet Med 2013
19
10

Respecting donors to biobank research.
Tom Tomlinson. Hastings Cent Rep 2013
21
9

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
6

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
227
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.