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: 11







List of co-cited articles
29 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
27
36

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
36

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
213
27

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
37
27

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
17
27

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
19
27

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
114
18

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
91
18

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
41
18

Cancer as a chronic disease.
Jane Louise Phillips, David C Currow. Collegian 2010
87
18


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
55
18

Engaging the public on biobanks: outcomes of the BC biobank deliberation.
K C O'Doherty, M M Burgess. Public Health Genomics 2009
67
18

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
15
18

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
34
18

Informed Consent.
Christine Grady, Steven R Cummings, Michael C Rowbotham, Michael V McConnell, Euan A Ashley, Gagandeep Kang. N Engl J Med 2017
84
18

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
15
18

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
20
18

Testing an online, dynamic consent portal for large population biobank research.
Daniel B Thiel, Jodyn Platt, Tevah Platt, Susan B King, Nicole Fisher, Robert Shelton, Sharon L R Kardia. Public Health Genomics 2015
25
18

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
26
18

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
13
18

Design Issues in E-Consent.
John Wilbanks. J Law Med Ethics 2018
20
18

An investigation of the efficacy of electronic consenting interfaces of research permissions management system in a hospital setting.
Kapil Chalil Madathil, Reshmi Koikkara, Jihad Obeid, Joel S Greenstein, Iain C Sanderson, Katrina Fryar, Jay Moskowitz, Anand K Gramopadhye. Int J Med Inform 2013
41
18

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
6
33

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
12
18

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
18

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
23
18

Current State of Electronic Consent Processes in Behavioral Health: Outcomes from an Observational Study.
Hiral Soni, Adela Grando, Anita Murcko, Mike Bayuk, Pramod Chandrashekar, Madhumita Mukundan, Meredith Abrams, Marcela P Aliste, Megan Hiestand, Julia Varkey,[...]. AMIA Annu Symp Proc 2018
5
40


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
123
9


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
18
9



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
13
9

SCIENTIFIC COMMUNITY. Confronting stem cell hype.
Timothy Caulfield, Douglas Sipp, Charles E Murry, George Q Daley, Jonathan Kimmelman. Science 2016
67
9

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
128
9



When Children Become Adults: Should Biobanks Re-Contact?
Noor A A Giesbertz, Annelien L Bredenoord, Johannes J M van Delden. PLoS Med 2016
7
14

Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
37
9

Obama's Precision Medicine Initiative.
Sharon F Terry. Genet Test Mol Biomarkers 2015
34
9

To the barricades!
Henry T Greely. Am J Bioeth 2010
10
10



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
81
9

Policy uncertainty, sequencing, and cell lines.
Timothy Caulfield, Amy L McGuire. G3 (Bethesda) 2013
7
14

Public opinion on policy issues in genetics and genomics.
Rene Almeling, Shana Kushner Gadarian. Genet Med 2014
13
9

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
36
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.