A citation-based method for searching scientific literature

Haridimos Kondylakis, Lefteris Koumakis, Stephanie Hänold, Iheanyi Nwankwo, Nikolaus Forgó, Kostas Marias, Manolis Tsiknakis, Norbert Graf. Int J Med Inform 2017
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


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
22
30

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
61
30

Teleconsent: A Novel Approach to Obtain Informed Consent for Research.
Brandon M Welch, Elizabeth Marshall, Suparna Qanungo, Ayesha Aziz, Marilyn Laken, Leslie Lenert, Jihad Obeid. Contemp Clin Trials Commun 2016
29
30

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
177
20

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
105
20

A review of the key issues associated with the commercialization of biobanks.
Timothy Caulfield, Sarah Burningham, Yann Joly, Zubin Master, Mahsa Shabani, Pascal Borry, Allan Becker, Michael Burgess, Kathryn Calder, Christine Critchley,[...]. J Law Biosci 2014
32
20

Cancer as a chronic disease.
Jane Louise Phillips, David C Currow. Collegian 2010
71
20

Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research.
Hawys Williams, Karen Spencer, Caroline Sanders, David Lund, Edgar A Whitley, Jane Kaye, William G Dixon. JMIR Med Inform 2015
47
20

Every participant is a PI. Citizen science and participatory governance in population studies.
Alena Buyx, Lorenzo Del Savio, Barbara Prainsack, Henry Völzke. Int J Epidemiol 2017
11
20

Formative Evaluation of Participant Experience With Mobile eConsent in the App-Mediated Parkinson mPower Study: A Mixed Methods Study.
Megan Doerr, Amy Maguire Truong, Brian M Bot, John Wilbanks, Christine Suver, Lara M Mangravite. JMIR Mhealth Uhealth 2017
29
20

Informed Consent.
Christine Grady, Steven R Cummings, Michael C Rowbotham, Michael V McConnell, Euan A Ashley, Gagandeep Kang. N Engl J Med 2017
73
20

A pragmatic randomized trial comparing tablet computer informed consent to traditional paper-based methods for an osteoporosis study.
A H Warriner, P J Foster, A Mudano, N C Wright, M E Melton, S E Sattui, W Calmbach, J R Curtis, M Kilgore, C E Lewis,[...]. Contemp Clin Trials Commun 2016
13
20

Traditional and electronic informed consent for biobanking: a survey of U.S. biobanks.
Christian M Simon, David W Klein, Helen A Schartz. Biopreserv Biobank 2014
18
20

Risk based survey evidence supports electronic informed consent as a recruitment method for UK clinical trials.
Natasha Stevens, Lara Edwards, Zuhur Balayah, Richard Hooper, Charles Knowles. J Clin Epidemiol 2016
5
40

Interactive multimedia consent for biobanking: a randomized trial.
Christian M Simon, David W Klein, Helen A Schartz. Genet Med 2016
22
20

Perspectives on Electronic Informed Consent From Patients Underrepresented in Research in the United States: A Focus Group Study.
Christian M Simon, Helen A Schartz, Gary E Rosenthal, Eric L Eisenstein, David W Klein. J Empir Res Hum Res Ethics 2018
11
20

Design Issues in E-Consent.
John Wilbanks. J Law Med Ethics 2018
16
20

Patient preferences toward an interactive e-consent application for research using electronic health records.
Christopher A Harle, Elizabeth H Golembiewski, Kiarash P Rahmanian, Janice L Krieger, Dorothy Hagmajer, Arch G Mainous, Ray E Moseley. J Am Med Inform Assoc 2018
15
20

MAGIC: once upon a time in consent management-a FHIR® tale.
Martin Bialke, Thomas Bahls, Lars Geidel, Henriette Rau, Arne Blumentritt, Sandra Pasewald, Robert Wolff, Jonas Steinmann, Tobias Bronsch, Björn Bergh,[...]. J Transl Med 2018
5
40

iCONCUR: informed consent for clinical data and bio-sample use for research.
Hyeoneui Kim, Elizabeth Bell, Jihoon Kim, Amy Sitapati, Joe Ramsdell, Claudiu Farcas, Dexter Friedman, Stephanie Feudjio Feupe, Lucila Ohno-Machado. J Am Med Inform Assoc 2017
17
20

mHealth and telemedicine apps: in search of a common regulation.
Chiara Crico, Chiara Renzi, Norbert Graf, Alena Buyx, Haridimos Kondylakis, Lefteris Koumakis, Gabriella Pravettoni. Ecancermedicalscience 2018
11
20

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
20

Features, outcomes, and challenges in mobile health interventions for patients living with chronic diseases: A review of systematic reviews.
Andreas Triantafyllidis, Haridimos Kondylakis, Konstantinos Votis, Dimitrios Tzovaras, Nicos Maglaveras, Kazem Rahimi. Int J Med Inform 2019
13
20


Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
108
10


Understanding the Public's Reservations about Broad Consent and Study-By-Study Consent for Donations to a Biobank: Results of a National Survey.
Raymond Gene De Vries, Tom Tomlinson, Hyungjin Myra Kim, Chris Krenz, Diana Haggerty, Kerry A Ryan, Scott Y H Kim. PLoS One 2016
15
10



No regrets: Young adult patients in psychiatry report positive reactions to biobank participation.
Janet L Cunningham, Manuel Zanzi, Mimmie Willebrand, Lisa Ekselius, Mia Ramklint. BMC Psychiatry 2017
8
12

SCIENTIFIC COMMUNITY. Confronting stem cell hype.
Timothy Caulfield, Douglas Sipp, Charles E Murry, George Q Daley, Jonathan Kimmelman. Science 2016
61
10

Public knowledge of and attitudes toward genetics and genetic testing.
Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
111
10



When Children Become Adults: Should Biobanks Re-Contact?
Noor A A Giesbertz, Annelien L Bredenoord, Johannes J M van Delden. PLoS Med 2016
5
20

Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
31
10

Obama's Precision Medicine Initiative.
Sharon F Terry. Genet Test Mol Biomarkers 2015
33
10

To the barricades!
Henry T Greely. Am J Bioeth 2010
9
11



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
69
10

Policy uncertainty, sequencing, and cell lines.
Timothy Caulfield, Amy L McGuire. G3 (Bethesda) 2013
5
20

Public opinion on policy issues in genetics and genomics.
Rene Almeling, Shana Kushner Gadarian. Genet Med 2014
11
10

Moral concerns and the willingness to donate to a research biobank.
Tom Tomlinson, Raymond De Vries, Kerry Ryan, Hyungjin Myra Kim, Nicole Lehpamer, Scott Y H Kim. JAMA 2015
31
10

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
72
10

Newspaper coverage of biobanks.
Ubaka Ogbogu, Maeghan Toews, Adam Ollenberger, Pascal Borry, Helene Nobile, Manuela Bergmann, Timothy Caulfield. PeerJ 2014
3
33

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
47
10


Confidentiality in Biobanking Research: A Comparison of Donor and Nondonor Families' Understanding of Risks.
Laura A Siminoff, Maureen Wilson-Genderson, Maghboeba Mosavel, Laura Barker, Jennifer Trgina, Heather M Traino. Genet Test Mol Biomarkers 2017
9
11

Public responses to the sharing and linkage of health data for research purposes: a systematic review and thematic synthesis of qualitative studies.
Mhairi Aitken, Jenna de St Jorre, Claudia Pagliari, Ruth Jepson, Sarah Cunningham-Burley. BMC Med Ethics 2016
69
10


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.