A citation-based method for searching scientific literature

Alessandro Blasimme, Effy Vayena. BMC Med Ethics 2016
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


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
27

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
22

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
81
22

Biomedical Big Data: New Models of Control Over Access, Use and Governance.
Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
29
22

From patients to partners: participant-centric initiatives in biomedical research.
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
159
18

Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiatives.
J Patrick Woolley, Michelle L McGowan, Harriet J A Teare, Victoria Coathup, Jennifer R Fishman, Richard A Settersten, Sigrid Sterckx, Jane Kaye, Eric T Juengst. BMC Med Ethics 2016
50
18

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
135
18

The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
111
18

Digital health: meeting the ethical and policy challenges.
Effy Vayena, Tobias Haeusermann, Afua Adjekum, Alessandro Blasimme. Swiss Med Wkly 2018
25
18

Patient and interest organizations' views on personalized medicine: a qualitative study.
Isabelle Budin-Ljøsne, Jennifer R Harris. BMC Med Ethics 2016
19
15

Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era.
Don Chalmers, Dianne Nicol, Jane Kaye, Jessica Bell, Alastair V Campbell, Calvin W L Ho, Kazuto Kato, Jusaku Minari, Chih-Hsing Ho, Colin Mitchell,[...]. BMC Med Ethics 2016
50
13

Medicine. Big data meets public health.
Muin J Khoury, John P A Ioannidis. Science 2014
140
13

Health data cooperatives - citizen empowerment.
E Hafen, D Kossmann, A Brand. Methods Inf Med 2014
46
13


Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
211
13

Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
23
13



Defining digital medicine.
Eric Elenko, Lindsay Underwood, Daphne Zohar. Nat Biotechnol 2015
71
13


Engaging the public on biobanks: outcomes of the BC biobank deliberation.
K C O'Doherty, M M Burgess. Public Health Genomics 2009
65
13

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
72
13

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
79
9


Big Data: Astronomical or Genomical?
Zachary D Stephens, Skylar Y Lee, Faraz Faghri, Roy H Campbell, Chengxiang Zhai, Miles J Efron, Ravishankar Iyer, Michael C Schatz, Saurabh Sinha, Gene E Robinson. PLoS Biol 2015
355
9

Should you profit from your genome?
Jessica L Roberts, Stacey Pereira, Amy L McGuire. Nat Biotechnol 2017
10
20

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
466
9

Informed Consent.
Christine Grady, Steven R Cummings, Michael C Rowbotham, Michael V McConnell, Euan A Ashley, Gagandeep Kang. N Engl J Med 2017
84
9

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
9

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
228
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
9

Precision medicine: Beyond the inflection point.
Sam Hawgood, India G Hook-Barnard, Theresa C O'Brien, Keith R Yamamoto. Sci Transl Med 2015
58
9

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
215
9

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
52
9

Digital drug safety surveillance: monitoring pharmaceutical products in twitter.
Clark C Freifeld, John S Brownstein, Christopher M Menone, Wenjie Bao, Ross Filice, Taha Kass-Hout, Nabarun Dasgupta. Drug Saf 2014
130
9

DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
69
9

Ethical endgames: broad consent for narrow interests; open consent for closed minds.
Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm. Camb Q Healthc Ethics 2011
18
11

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
39
9

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
92
9

Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
64
9

What makes clinical research ethical?
E J Emanuel, D Wendler, C Grady. JAMA 2000
9

Ethical challenges of big data in public health.
Effy Vayena, Marcel Salathé, Lawrence C Madoff, John S Brownstein. PLoS Comput Biol 2015
98
9

Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
32
9

Policy implications of big data in the health sector.
Effy Vayena, Joan Dzenowagis, John S Brownstein, Aziz Sheikh. Bull World Health Organ 2018
27
9

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


Have we asked too much of consent?
Barbara A Koenig. Hastings Cent Rep 2014
44
9

Informed consent: a broken contract.
Erika Check Hayden. Nature 2012
29
9

Respecting donors to biobank research.
Tom Tomlinson. Hastings Cent Rep 2013
21
9



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.