A citation-based method for searching scientific literature

Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
Times Cited: 27







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



Times Cited
  Times     Co-cited
Similarity


Biomedical Big Data: New Models of Control Over Access, Use and Governance.
Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
21
23

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
18

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
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

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
11

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
93
11

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
420
11

Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
93
11

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
61
11

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
80
11


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
7

The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
94
7

Blockchain technology for improving clinical research quality.
Mehdi Benchoufi, Philippe Ravaud. Trials 2017
34
7

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
50

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
7


Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
38
7

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


Big Data Application in Biomedical Research and Health Care: A Literature Review.
Jake Luo, Min Wu, Deepika Gopukumar, Yiqing Zhao. Biomed Inform Insights 2016
68
7

The inevitable application of big data to health care.
Travis B Murdoch, Allan S Detsky. JAMA 2013
470
7




The ethics of participant-led biomedical research.
Effy Vayena, John Tasioulas. Nat Biotechnol 2013
19
10

Open sharing of genomic data: Who does it and why?
Tobias Haeusermann, Bastian Greshake, Alessandro Blasimme, Darja Irdam, Martin Richards, Effy Vayena. PLoS One 2017
25
8


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
7

Data Sharing For Precision Medicine: Policy Lessons And Future Directions.
Alessandro Blasimme, Marta Fadda, Manuel Schneider, Effy Vayena. Health Aff (Millwood) 2018
12
16


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
412
7

A risk-based framework for biomedical data sharing.
Fida K Dankar, Radja Badji. J Biomed Inform 2017
5
40

Implementation of Electronic Consent at a Biobank: An Opportunity for Precision Medicine Research.
Natalie T Boutin, Kathleen Mathieu, Alison G Hoffnagle, Nicole L Allen, Victor M Castro, Megan Morash, P Pearl O'Rourke, Elizabeth L Hohmann, Neil Herring, Lynn Bry,[...]. J Pers Med 2016
22
9


The personal genome project.
G M Church. Mol Syst Biol 2005
106
7

Challenges of web-based personal genomic data sharing.
Mahsa Shabani, Pascal Borry. Life Sci Soc Policy 2015
12
16


Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials.
Adam Nishimura, Jantey Carey, Patricia J Erwin, Jon C Tilburt, M Hassan Murad, Jennifer B McCormick. BMC Med Ethics 2013
201
7


Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan.
Victoria Coathup, Harriet J A Teare, Jusaku Minari, Go Yoshizawa, Jane Kaye, Masanori P Takahashi, Kazuto Kato. BMC Med Ethics 2016
14
14

Don't just invite us to the table: authentic community engagement.
Sharon F Terry. Genet Test Mol Biomarkers 2013
8
25


Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
41
7

The RUDY study platform - a novel approach to patient driven research in rare musculoskeletal diseases.
M K Javaid, L Forestier-Zhang, L Watts, A Turner, C Ponte, H Teare, D Gray, N Gray, R Popert, J Hogg,[...]. Orphanet J Rare Dis 2016
20
10


An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
228
7

A Belmont Report for Health Data.
Efthimios Parasidis, Elizabeth Pike, Deven McGraw. N Engl J Med 2019
12
16

Privacy in the age of medical big data.
W Nicholson Price, I Glenn Cohen. Nat Med 2019
65
7



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.