A citation-based method for searching scientific literature

Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
Times Cited: 31







List of co-cited articles
84 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
29
20

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
133
16

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
12

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
90
12

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

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
9

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
110
9

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
463
9

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
117
9

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
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
120
6

The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
110
6

Blockchain technology for improving clinical research quality.
Mehdi Benchoufi, Philippe Ravaud. Trials 2017
39
6

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
40

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
6


Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
43
6

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


Protecting human research participants in the age of big data.
Susan T Fiske, Robert M Hauser. Proc Natl Acad Sci U S A 2014
18
11


Big Data Application in Biomedical Research and Health Care: A Literature Review.
Jake Luo, Min Wu, Deepika Gopukumar, Yiqing Zhao. Biomed Inform Insights 2016
76
6


The inevitable application of big data to health care.
Travis B Murdoch, Allan S Detsky. JAMA 2013
523
6




The ethics of participant-led biomedical research.
Effy Vayena, John Tasioulas. Nat Biotechnol 2013
21
9

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
27
7


Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
132
6

Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results.
J Scott Roberts, Michele C Gornick, Deanna Alexis Carere, Wendy R Uhlmann, Mack T Ruffin, Robert C Green. Public Health Genomics 2017
57
6

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
34
6

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

Reimagining Human Research Protections for 21st Century Science.
Cinnamon Bloss, Camille Nebeker, Matthew Bietz, Deborah Bae, Barbara Bigby, Mary Devereaux, James Fowler, Ann Waldo, Nadir Weibel, Kevin Patrick,[...]. J Med Internet Res 2016
21
9

Engaging research participants to inform the ethical conduct of mobile imaging, pervasive sensing, and location tracking research.
Camille Nebeker, Tiffany Lagare, Michelle Takemoto, Brittany Lewars, Katie Crist, Cinnamon S Bloss, Jacqueline Kerr. Transl Behav Med 2016
32
6

Ethical and regulatory challenges of research using pervasive sensing and other emerging technologies: IRB perspectives.
Camille Nebeker, John Harlow, Rebeca Espinoza Giacinto, Rubi Orozco-Linares, Cinnamon S Bloss, Nadir Weibel. AJOB Empir Bioeth 2017
31
6



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
444
6

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
26
7


The personal genome project.
G M Church. Mol Syst Biol 2005
122
6

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
225
6


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


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.