A citation-based method for searching scientific literature

Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
Times Cited: 43







List of co-cited articles
131 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
34
17

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
156
13

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
58
13

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
150
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
115
11

Privacy in the age of medical big data.
W Nicholson Price, I Glenn Cohen. Nat Med 2019
186
11

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
499
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
45
9

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
104
9

A Belmont Report for Health Data.
Efthimios Parasidis, Elizabeth Pike, Deven McGraw. N Engl J Med 2019
17
23

The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
146
9

Policy implications of big data in the health sector.
Effy Vayena, Joan Dzenowagis, John S Brownstein, Aziz Sheikh. Bull World Health Organ 2018
33
9

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
6

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
139
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
41
7

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
133
6

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
308
6

Big Data, Big Tech, and Protecting Patient Privacy.
I Glenn Cohen, Michelle M Mello. JAMA 2019
41
7

The FAIR Guiding Principles for scientific data management and stewardship.
Mark D Wilkinson, Michel Dumontier, I Jsbrand Jan Aalbersberg, Gabrielle Appleton, Myles Axton, Arie Baak, Niklas Blomberg, Jan-Willem Boiten, Luiz Bonino da Silva Santos, Philip E Bourne,[...]. Sci Data 2016
6

Implementing Machine Learning in Health Care - Addressing Ethical Challenges.
Danton S Char, Nigam H Shah, David Magnus. N Engl J Med 2018
327
6

Dissecting racial bias in an algorithm used to manage the health of populations.
Ziad Obermeyer, Brian Powers, Christine Vogeli, Sendhil Mullainathan. Science 2019
704
6


Authority and the Future of Consent in Population-Level Biomedical Research.
Mark Sheehan, Rachel Thompson, Jon Fistein, Jim Davies, Michael Dunn, Michael Parker, Julian Savulescu, Kerrie Woods. Public Health Ethics 2019
14
21

Of Straws, Camels, Research Regulation, and IRBs.
Phoebe Friesen, Barbara Redman, Arthur Caplan. Ther Innov Regul Sci 2019
6
50



Ethics review of big data research: What should stay and what should be reformed?
Agata Ferretti, Marcello Ienca, Mark Sheehan, Alessandro Blasimme, Edward S Dove, Bobbie Farsides, Phoebe Friesen, Jeff Kahn, Walter Karlen, Peter Kleist,[...]. BMC Med Ethics 2021
8
37


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
160
4

The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
145
4

Blockchain technology for improving clinical research quality.
Mehdi Benchoufi, Philippe Ravaud. Trials 2017
46
4

Data sharing by scientists: practices and perceptions.
Carol Tenopir, Suzie Allard, Kimberly Douglass, Arsev Umur Aydinoglu, Lei Wu, Eleanor Read, Maribeth Manoff, Mike Frame. PLoS One 2011
205
4

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
96
4


Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
49
4

Digital health: meeting the ethical and policy challenges.
Effy Vayena, Tobias Haeusermann, Afua Adjekum, Alessandro Blasimme. Swiss Med Wkly 2018
36
5

Grand challenges in digital health.
Patty Kostkova. Front Public Health 2015
49
4

Protecting human research participants in the age of big data.
Susan T Fiske, Robert M Hauser. Proc Natl Acad Sci U S A 2014
19
10


Ten simple rules for responsible big data research.
Matthew Zook, Solon Barocas, Danah Boyd, Kate Crawford, Emily Keller, Seeta Peña Gangadharan, Alyssa Goodman, Rachelle Hollander, Barbara A Koenig, Jacob Metcalf,[...]. PLoS Comput Biol 2017
53
4

Big Data Application in Biomedical Research and Health Care: A Literature Review.
Jake Luo, Min Wu, Deepika Gopukumar, Yiqing Zhao. Biomed Inform Insights 2016
104
4


Ethical challenges of big data in public health.
Effy Vayena, Marcel Salathé, Lawrence C Madoff, John S Brownstein. PLoS Comput Biol 2015
110
4


The inevitable application of big data to health care.
Travis B Murdoch, Allan S Detsky. JAMA 2013
605
4


HIPAA and Protecting Health Information in the 21st Century.
I Glenn Cohen, Michelle M Mello. JAMA 2018
49
4


Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.
J M Oliver, M J Slashinski, T Wang, P A Kelly, S G Hilsenbeck, A L McGuire. Public Health Genomics 2012
78
4


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.