A citation-based method for searching scientific literature

Laura Mählmann, Sebastian Schee Gen Halfmann, Agnes von Wyl, Angela Brand. Public Health Genomics 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


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
112
50

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
393
50

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
62
50

Anonymising and sharing individual patient data.
Khaled El Emam, Sam Rodgers, Bradley Malin. BMJ 2015
43
25

Swiss Learning Health System: A national initiative to establish learning cycles for continuous health system improvement.
Stefan Boes, Sarah Mantwill, Cornel Kaufmann, Mirjam Brach, Jerome Bickenbach, Sara Rubinelli, Gerold Stucki.  2018
1
100

Clinical Data Reuse or Secondary Use: Current Status and Potential Future Progress.
S M Meystre, C Lovis, T Bürkle, G Tognola, A Budrionis, C U Lehmann. Yearb Med Inform 2017
24
25

The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
79
25

Consent requirements for research with human tissue: Swiss ethics committee members disagree.
Flora Colledge, Sophie De Massougnes, Bernice Elger. BMC Med Ethics 2018
3
33

A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur. J. Hum. Genet. 2013
47
25

Translational machine learning for psychiatric neuroimaging.
Martin Walter, Sarah Alizadeh, Hamidreza Jamalabadi, Ulrike Lueken, Udo Dannlowski, Henrik Walter, Sebastian Olbrich, Lejla Colic, Joseph Kambeitz, Nikolaos Koutsouleris,[...]. Prog. Neuropsychopharmacol. Biol. Psychiatry 2019
7
25

Public preferences about secondary uses of electronic health information.
David Grande, Nandita Mitra, Anand Shah, Fei Wan, David A Asch. JAMA Intern Med 2013
75
25


Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to consider.
Amy L McGuire, Rebecca Fisher, Paul Cusenza, Kathy Hudson, Mark A Rothstein, Deven McGraw, Stephen Matteson, John Glaser, Douglas E Henley. Genet. Med. 2008
37
25

Secondary use of clinical data.
Peter L Elkin, Brett E Trusko, Ross Koppel, Ted Speroff, Daniel Mohrer, Saoussen Sakji, Inna Gurewitz, Mark Tuttle, Steven H Brown. Stud Health Technol Inform 2010
17
25

Mining electronic health records: towards better research applications and clinical care.
Peter B Jensen, Lars J Jensen, Søren Brunak. Nat. Rev. Genet. 2012
425
25

Are Patients With Cancer Less Willing to Share Their Health Information? Privacy, Sensitivity, and Social Purpose.
David Grande, David A Asch, Fei Wan, Angela R Bradbury, Reshma Jagsi, Nandita Mitra. J Oncol Pract 2015
12
25

Trustworthy reuse of health data: a transnational perspective.
A Geissbuhler, C Safran, I Buchan, R Bellazzi, S Labkoff, K Eilenberg, A Leese, C Richardson, J Mantas, P Murray,[...]. Int J Med Inform 2013
32
25


The Learning Healthcare System: Where are we now? A systematic review.
Andrius Budrionis, Johan Gustav Bellika. J Biomed Inform 2016
37
25


Reducing patient re-identification risk for laboratory results within research datasets.
Ravi V Atreya, Joshua C Smith, Allison B McCoy, Bradley Malin, Randolph A Miller. J Am Med Inform Assoc 2013
9
25

Big data in biomedicine.
Fabricio F Costa. Drug Discov. Today 2014
58
25

Big Data and Machine Learning in Health Care.
Andrew L Beam, Isaac S Kohane. JAMA 2018
183
25

Demonstrating "collect once, use many"--assimilating public health secondary data use requirements into an existing Domain Analysis Model.
Cynthia Barton, Crystal Kallem, Patricia Van Dyke, Donald Mon, Rachel Richesson. AMIA Annu Symp Proc 2011
4
25

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
Catherine A McCarty, Rex L Chisholm, Christopher G Chute, Iftikhar J Kullo, Gail P Jarvik, Eric B Larson, Rongling Li, Daniel R Masys, Marylyn D Ritchie, Dan M Roden,[...]. BMC Med Genomics 2011
396
25

The inconsistent ethical oversight of healthcare quality data in Switzerland.
Stuart McLennan, Roxanne Maritz, David Shaw, Bernice Elger. Swiss Med Wkly 2018
1
100

South Korea: in the midst of a privacy reform centered on data sharing.
Hannah Kim, So Yoon Kim, Yann Joly. Hum. Genet. 2018
4
25

Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper.
Charles Safran, Meryl Bloomrosen, W Edward Hammond, Steven Labkoff, Suzanne Markel-Fox, Paul C Tang, Don E Detmer, Expert Panel. J Am Med Inform Assoc 2007
246
25

Primary and secondary patient data in contrast: the use of observational studies like RABBIT.
Adrian Richter, Yvette Meißner, Anja Strangfeld, Angela Zink. Clin. Exp. Rheumatol. 2016
4
25

Influenza forecasting with Google Flu Trends.
Andrea Freyer Dugas, Mehdi Jalalpour, Yulia Gel, Scott Levin, Fred Torcaso, Takeru Igusa, Richard E Rothman. PLoS ONE 2013
98
25

Genetic exceptionalism. Too much of a good thing?
James P Evans, Wylie Burke. Genet. Med. 2008
18
25


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
110
25

Drafting the Genetic Privacy Act: science, policy, and practical considerations.
G J Annas, L H Glantz, P A Roche. J Law Med Ethics 1995
53
25




Secondary Use and Analysis of Big Data Collected for Patient Care.
F J Martin-Sanchez, V Aguiar-Pulido, G H Lopez-Campos, N Peek, L Sacchi. Yearb Med Inform 2017
6
25



Genetic risk prediction in complex disease.
Luke Jostins, Jeffrey C Barrett. Hum. Mol. Genet. 2011
103
25


Public perspectives regarding data-sharing practices in genomics research.
S B Haga, J O'Daniel. Public Health Genomics 2011
25
25

Pediatric data sharing in genomic research: attitudes and preferences of parents.
Matthew D Burstein, Jill Oliver Robinson, Susan G Hilsenbeck, Amy L McGuire, Ching C Lau. Pediatrics 2014
19
25

Creating a data resource: what will it take to build a medical information commons?
Patricia A Deverka, Mary A Majumder, Angela G Villanueva, Margaret Anderson, Annette C Bakker, Jessica Bardill, Eric Boerwinkle, Tania Bubela, Barbara J Evans, Nanibaa' A Garrison,[...]. Genome Med 2017
19
25


Balancing Benefits and Risks of Immortal Data: Participants' Views of Open Consent in the Personal Genome Project.
Oscar A Zarate, Julia Green Brody, Phil Brown, Mónica D Ramirez-Andreotta, Laura Perovich, Jacob Matz. Hastings Cent Rep 2016
14
25

Including all voices in international data-sharing governance.
Jane Kaye, Sharon F Terry, Eric Juengst, Sarah Coy, Jennifer R Harris, Don Chalmers, Edward S Dove, Isabelle Budin-Ljøsne, Clement Adebamowo, Emilomo Ogbe,[...]. Hum. Genomics 2018
9
25

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
398
25

Ethical, legal, and social implications of incorporating genomic information into electronic health records.
Ribhi Hazin, Kyle B Brothers, Bradley A Malin, Barbara A Koenig, Saskia C Sanderson, Mark A Rothstein, Marc S Williams, Ellen W Clayton, Iftikhar J Kullo. Genet. Med. 2013
52
25


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.