Haridimos Kondylakis, Lefteris Koumakis, Stephanie Hänold, Iheanyi Nwankwo, Nikolaus Forgó, Kostas Marias, Manolis Tsiknakis, Norbert Graf. Int J Med Inform 2017
Times Cited: 10
Times Cited: 10
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
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
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
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
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
Brandon M Welch, Elizabeth Marshall, Suparna Qanungo, Ayesha Aziz, Marilyn Laken, Leslie Lenert, Jihad Obeid. Contemp Clin Trials Commun 2016
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
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
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
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
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
Timothy Caulfield, Sarah Burningham, Yann Joly, Zubin Master, Mahsa Shabani, Pascal Borry, Allan Becker, Michael Burgess, Kathryn Calder, Christine Critchley,[...]. J Law Biosci 2014
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
Hawys Williams, Karen Spencer, Caroline Sanders, David Lund, Edgar A Whitley, Jane Kaye, William G Dixon. JMIR Med Inform 2015
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
Alena Buyx, Lorenzo Del Savio, Barbara Prainsack, Henry Völzke. Int J Epidemiol 2017
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
Megan Doerr, Amy Maguire Truong, Brian M Bot, John Wilbanks, Christine Suver, Lara M Mangravite. JMIR Mhealth Uhealth 2017
20
Informed Consent.
Christine Grady, Steven R Cummings, Michael C Rowbotham, Michael V McConnell, Euan A Ashley, Gagandeep Kang. N Engl J Med 2017
Christine Grady, Steven R Cummings, Michael C Rowbotham, Michael V McConnell, Euan A Ashley, Gagandeep Kang. N Engl J Med 2017
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
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
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
Christian M Simon, David W Klein, Helen A Schartz. Biopreserv Biobank 2014
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
Natasha Stevens, Lara Edwards, Zuhur Balayah, Richard Hooper, Charles Knowles. J Clin Epidemiol 2016
40
Interactive multimedia consent for biobanking: a randomized trial.
Christian M Simon, David W Klein, Helen A Schartz. Genet Med 2016
Christian M Simon, David W Klein, Helen A Schartz. Genet Med 2016
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
Christian M Simon, Helen A Schartz, Gary E Rosenthal, Eric L Eisenstein, David W Klein. J Empir Res Hum Res Ethics 2018
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
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
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
Martin Bialke, Thomas Bahls, Lars Geidel, Henriette Rau, Arne Blumentritt, Sandra Pasewald, Robert Wolff, Jonas Steinmann, Tobias Bronsch, Björn Bergh,[...]. J Transl Med 2018
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
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
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
Chiara Crico, Chiara Renzi, Norbert Graf, Alena Buyx, Haridimos Kondylakis, Lefteris Koumakis, Gabriella Pravettoni. Ecancermedicalscience 2018
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
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
Andreas Triantafyllidis, Haridimos Kondylakis, Konstantinos Votis, Dimitrios Tzovaras, Nicos Maglaveras, Kazem Rahimi. Int J Med Inform 2019
20
Finland on a road towards a modern legal biobanking infrastructure.
Sirpa Soini. Eur J Health Law 2013
Sirpa Soini. Eur J Health Law 2013
11
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
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
10
Understanding the impact of commercialization on public support for scientific research: is it about the funding source or the organization conducting the research.
Christine R Critchley, Dianne Nicol. Public Underst Sci 2011
Christine R Critchley, Dianne Nicol. Public Underst Sci 2011
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
Raymond Gene De Vries, Tom Tomlinson, Hyungjin Myra Kim, Chris Krenz, Diana Haggerty, Kerry A Ryan, Scott Y H Kim. PLoS One 2016
10
Clinical genomics, big data, and electronic medical records: reconciling patient rights with research when privacy and science collide.
Jennifer Kulynych, Henry T Greely. J Law Biosci 2017
Jennifer Kulynych, Henry T Greely. J Law Biosci 2017
10
Global trends on fears and concerns of genetic discrimination: a systematic literature review.
Annet Wauters, Ine Van Hoyweghen. J Hum Genet 2016
Annet Wauters, Ine Van Hoyweghen. J Hum Genet 2016
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
Janet L Cunningham, Manuel Zanzi, Mimmie Willebrand, Lisa Ekselius, Mia Ramklint. BMC Psychiatry 2017
12
SCIENTIFIC COMMUNITY. Confronting stem cell hype.
Timothy Caulfield, Douglas Sipp, Charles E Murry, George Q Daley, Jonathan Kimmelman. Science 2016
Timothy Caulfield, Douglas Sipp, Charles E Murry, George Q Daley, Jonathan Kimmelman. Science 2016
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
Susanne B Haga, William T Barry, Rachel Mills, Geoffrey S Ginsburg, Laura Svetkey, Jennifer Sullivan, Huntington F Willard. Genet Test Mol Biomarkers 2013
10
Controversial patient-consent proposal left out of research-ethics reforms.
Sara Reardon. Nature 2017
Sara Reardon. Nature 2017
50
Open consent, biobanking and data protection law: can open consent be 'informed' under the forthcoming data protection regulation?
Dara Hallinan, Michael Friedewald. Life Sci Soc Policy 2015
Dara Hallinan, Michael Friedewald. Life Sci Soc Policy 2015
10
When Children Become Adults: Should Biobanks Re-Contact?
Noor A A Giesbertz, Annelien L Bredenoord, Johannes J M van Delden. PLoS Med 2016
Noor A A Giesbertz, Annelien L Bredenoord, Johannes J M van Delden. PLoS Med 2016
20
Biobanking, consent, and control: a survey of Albertans on key research ethics issues.
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
Timothy Caulfield, Christen Rachul, Erin Nelson. Biopreserv Biobank 2012
10
100
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
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
10
Policy uncertainty, sequencing, and cell lines.
Timothy Caulfield, Amy L McGuire. G3 (Bethesda) 2013
Timothy Caulfield, Amy L McGuire. G3 (Bethesda) 2013
20
Public opinion on policy issues in genetics and genomics.
Rene Almeling, Shana Kushner Gadarian. Genet Med 2014
Rene Almeling, Shana Kushner Gadarian. Genet Med 2014
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
Tom Tomlinson, Raymond De Vries, Kerry Ryan, Hyungjin Myra Kim, Nicole Lehpamer, Scott Y H Kim. JAMA 2015
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
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
10
Newspaper coverage of biobanks.
Ubaka Ogbogu, Maeghan Toews, Adam Ollenberger, Pascal Borry, Helene Nobile, Manuela Bergmann, Timothy Caulfield. PeerJ 2014
Ubaka Ogbogu, Maeghan Toews, Adam Ollenberger, Pascal Borry, Helene Nobile, Manuela Bergmann, Timothy Caulfield. PeerJ 2014
33
Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
10
Revamping the US Federal Common Rule: Modernizing Human Participant Research Regulations.
James G Hodge, Lawrence O Gostin. JAMA 2017
James G Hodge, Lawrence O Gostin. JAMA 2017
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
Laura A Siminoff, Maureen Wilson-Genderson, Maghboeba Mosavel, Laura Barker, Jennifer Trgina, Heather M Traino. Genet Test Mol Biomarkers 2017
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
Mhairi Aitken, Jenna de St Jorre, Claudia Pagliari, Ruth Jepson, Sarah Cunningham-Burley. BMC Med Ethics 2016
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.