A citation-based method for searching scientific literature

Vilhjalmur Arnason. Bioethics 2004
Times Cited: 75







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



Times Cited
  Times     Co-cited
Similarity



Nationwide citizen access to their health data: analysing and comparing experiences in Denmark, Estonia and Australia.
Christian Nøhr, Liisa Parv, Pille Kink, Elizabeth Cummings, Helen Almond, Jens Rahbek Nørgaard, Paul Turner. BMC Health Serv Res 2017
25
4

Data Resource Profile: The New Zealand Integrated Data Infrastructure (IDI).
Barry J Milne, June Atkinson, Tony Blakely, Hilary Day, Jeroen Douwes, Sheree Gibb, Meisha Nicolson, Nichola Shackleton, Andrew Sporle, Andrea Teng. Int J Epidemiol 2019
20
5

Data protection and biomedical research in Switzerland: setting the record straight.
Andrea Martani, Philipp Egli, Michael Widmer, Bernice Elger. Swiss Med Wkly 2020
3
33


eHealth in Switzerland - building consensus, awareness and architecture.
Christian Lovis, Hansjorg Looser, Adrian Schmid, Judith Wagner, Stefan Wyss. Stud Health Technol Inform 2011
2
50

The promise of real-world data.
Hannah Stower. Nat Med 2019
4
25


Factors influencing harmonized health data collection, sharing and linkage in Denmark and Switzerland: A systematic review.
Lester Darryl Geneviève, Andrea Martani, Maria Christina Mallet, Tenzin Wangmo, Bernice Simone Elger. PLoS One 2019
6
16

Using electronic health records for clinical research: the case of the EHR4CR project.
Georges De Moor, Mats Sundgren, Dipak Kalra, Andreas Schmidt, Martin Dugas, Brecht Claerhout, Töresin Karakoyun, Christian Ohmann, Pierre-Yves Lastic, Nadir Ammour,[...]. J Biomed Inform 2015
80
1


Using Health Insurance Network Provider Data and Public Data Sets to Identify SARS-CoV-2 Vaccinators in the USA.
John R Litaker, Naomi Tamez, Wesley Durkalski, Richard Taylor. Front Public Health 2021
1
100

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
39
2


Switzerland: Health System Review.
Carlo De Pietro, Paul Camenzind, Isabelle Sturny, Luca Crivelli, Suzanne Edwards-Garavoglia, Anne Spranger, Friedrich Wittenbecher, Wilm Quentin. Health Syst Transit 2015
75
1

Enhancing Reuse of Data and Biological Material in Medical Research: From FAIR to FAIR-Health.
Petr Holub, Florian Kohlmayer, Fabian Prasser, Michaela Th Mayrhofer, Irene Schlünder, Gillian M Martin, Sara Casati, Lefteris Koumakis, Andrea Wutte, Łukasz Kozera,[...]. Biopreserv Biobank 2018
15
6

Editorial: The Use of Routine Health Data in Low- and Middle-Income Countries.
Jim Todd, Michael Johnson Mahande. Front Public Health 2020
1
100

A qualitative study of Canada's experience with the implementation of electronic health information technology.
Ronen Rozenblum, Yeona Jang, Eyal Zimlichman, Claudia Salzberg, Melissa Tamblyn, David Buckeridge, Alan Forster, David W Bates, Robyn Tamblyn. CMAJ 2011
31
3

The Nordic countries as a cohort for pharmacoepidemiological research.
Kari Furu, Björn Wettermark, Morten Andersen, Jaana E Martikainen, Anna Birna Almarsdottir, Henrik Toft Sørensen. Basic Clin Pharmacol Toxicol 2010
358
1

Regional Variation of Cost of Care in the Last 12 Months of Life in Switzerland: Small-area Analysis Using Insurance Claims Data.
Radoslaw Panczak, Xhyljeta Luta, Maud Maessen, Andreas E Stuck, Claudia Berlin, Kurt Schmidlin, Oliver Reich, Viktor von Wyl, David C Goodman, Matthias Egger,[...]. Med Care 2017
17
5

Unpatients-why patients should own their medical data.
Leonard J Kish, Eric J Topol. Nat Biotechnol 2015
33
3


The International Cancer Genome Consortium Data Portal.
Junjun Zhang, Rosita Bajari, Dusan Andric, Francois Gerthoffert, Alexandru Lepsa, Hardeep Nahal-Bose, Lincoln D Stein, Vincent Ferretti. Nat Biotechnol 2019
74
1

Cohort profile of the CARTaGENE study: Quebec's population-based biobank for public health and personalized genomics.
Philip Awadalla, Catherine Boileau, Yves Payette, Youssef Idaghdour, Jean-Philippe Goulet, Bartha Knoppers, Pavel Hamet, Claude Laberge. Int J Epidemiol 2013
96
1


How to fix the GDPR's frustration of global biomedical research.
Jasper Bovenberg, David Peloquin, Barbara Bierer, Mark Barnes, Bartha Maria Knoppers. Science 2020
11
9

Cohort Profile: Alberta's Tomorrow Project.
Ming Ye, Paula J Robson, Dean T Eurich, Jennifer E Vena, Jian-Yi Xu, Jeffrey A Johnson. Int J Epidemiol 2017
18
5

The Cambridge Analytica affair and Internet-mediated research.
Christophe Olivier Schneble, Bernice Simone Elger, David Shaw. EMBO Rep 2018
7
14


UK Biobank: from concept to reality.
William Ollier, Tim Sprosen, Tim Peakman. Pharmacogenomics 2005
104
1


An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
1

Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.
Pooja Middha Kapoor, Nasim Mavaddat, Parichoy Pal Choudhury, Amber N Wilcox, Sara Lindström, Sabine Behrens, Kyriaki Michailidou, Joe Dennis, Manjeet K Bolla, Qin Wang,[...]. J Natl Cancer Inst 2021
9
11

The International Rare Diseases Research Consortium: Policies and Guidelines to maximize impact.
Hanns Lochmüller, Josep Torrent I Farnell, Yann Le Cam, Anneliene H Jonker, Lilian Pl Lau, Gareth Baynam, Petra Kaufmann, Hugh Js Dawkins, Paul Lasko, Christopher P Austin,[...]. Eur J Hum Genet 2017
32
3


The law of genetic privacy: applications, implications, and limitations.
Ellen Wright Clayton, Barbara J Evans, James W Hazel, Mark A Rothstein. J Law Biosci 2019
29
3


The Genetic Family as Patient?
Bartha Maria Knoppers, Kristina Kekesi-Lafrance. Am J Bioeth 2020
4
25

Who's on third? Regulation of third-party genetic interpretation services.
Christi J Guerrini, Jennifer K Wagner, Sarah C Nelson, Gail H Javitt, Amy L McGuire. Genet Med 2020
14
7

Genetic privacy.
L O Gostin. J Law Med Ethics 1995
42
2

Examining the power of the social imaginary through competing narratives of data ownership in health research.
Annie Sorbie, Wifak Gueddana, Graeme Laurie, David Townend. J Law Biosci 2021
1
100

Pioneers in medicine.
Holger Breithaupt. EMBO Rep 2003
1
100


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.