Effy Vayena, Alessandro Blasimme. J Bioeth Inq 2017
Times Cited: 34
Times Cited: 34
Times Cited
Times Co-cited
Similarity
Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
17
Becoming partners, retaining autonomy: ethical considerations on the development of precision medicine.
Alessandro Blasimme, Effy Vayena. BMC Med Ethics 2016
Alessandro Blasimme, Effy Vayena. BMC Med Ethics 2016
21
The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
14
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
14
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
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
11
11
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
11
Considerations for ethics review of big data health research: A scoping review.
Marcello Ienca, Agata Ferretti, Samia Hurst, Milo Puhan, Christian Lovis, Effy Vayena. PLoS One 2018
Marcello Ienca, Agata Ferretti, Samia Hurst, Milo Puhan, Christian Lovis, Effy Vayena. PLoS One 2018
11
8
Google DeepMind and healthcare in an age of algorithms.
Julia Powles, Hal Hodson. Health Technol (Berl) 2017
Julia Powles, Hal Hodson. Health Technol (Berl) 2017
8
Policy implications of big data in the health sector.
Effy Vayena, Joan Dzenowagis, John S Brownstein, Aziz Sheikh. Bull World Health Organ 2018
Effy Vayena, Joan Dzenowagis, John S Brownstein, Aziz Sheikh. Bull World Health Organ 2018
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
Alessandro Blasimme, Celine Moret, Samia A Hurst, Effy Vayena. Am J Bioeth 2017
60
The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
Brent Daniel Mittelstadt, Luciano Floridi. Sci Eng Ethics 2016
8
Broad versus blanket consent for research with human biological samples.
David Wendler. Hastings Cent Rep 2013
David Wendler. Hastings Cent Rep 2013
15
Barbarians at the Gate: Consumer-Driven Health Data Commons and the Transformation of Citizen Science.
Barbara J Evans. Am J Law Med 2016
Barbara J Evans. Am J Law Med 2016
13
Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
8
The other side of the coin: Harm due to the non-use of health-related data.
Kerina H Jones, Graeme Laurie, Leslie Stevens, Christine Dobbs, David V Ford, Nathan Lea. Int J Med Inform 2017
Kerina H Jones, Graeme Laurie, Leslie Stevens, Christine Dobbs, David V Ford, Nathan Lea. Int J Med Inform 2017
8
Big data analytics to improve cardiovascular care: promise and challenges.
John S Rumsfeld, Karen E Joynt, Thomas M Maddox. Nat Rev Cardiol 2016
John S Rumsfeld, Karen E Joynt, Thomas M Maddox. Nat Rev Cardiol 2016
8
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
8
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
8
The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
8
8
Unpatients-why patients should own their medical data.
Leonard J Kish, Eric J Topol. Nat Biotechnol 2015
Leonard J Kish, Eric J Topol. Nat Biotechnol 2015
8
Protecting Your Patients' Interests in the Era of Big Data, Artificial Intelligence, and Predictive Analytics.
Patricia Balthazar, Peter Harri, Adam Prater, Nabile M Safdar. J Am Coll Radiol 2018
Patricia Balthazar, Peter Harri, Adam Prater, Nabile M Safdar. J Am Coll Radiol 2018
8
Future-proofing biobanks' governance.
Felix Gille, Effy Vayena, Alessandro Blasimme. Eur J Hum Genet 2020
Felix Gille, Effy Vayena, Alessandro Blasimme. Eur J Hum Genet 2020
23
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
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
10
Big health data: the need to earn public trust.
Tjeerd-Pieter van Staa, Ben Goldacre, Iain Buchan, Liam Smeeth. BMJ 2016
Tjeerd-Pieter van Staa, Ben Goldacre, Iain Buchan, Liam Smeeth. BMJ 2016
8
Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure.
Madeleine J Murtagh, Mwenza T Blell, Olly W Butters, Lorraine Cowley, Edward S Dove, Alissa Goodman, Rebecca L Griggs, Alison Hall, Nina Hallowell, Meena Kumari,[...]. Hum Genomics 2018
Madeleine J Murtagh, Mwenza T Blell, Olly W Butters, Lorraine Cowley, Edward S Dove, Alissa Goodman, Rebecca L Griggs, Alison Hall, Nina Hallowell, Meena Kumari,[...]. Hum Genomics 2018
18
Ethics and Epistemology in Big Data Research.
Wendy Lipworth, Paul H Mason, Ian Kerridge, John P A Ioannidis. J Bioeth Inq 2017
Wendy Lipworth, Paul H Mason, Ian Kerridge, John P A Ioannidis. J Bioeth Inq 2017
9
Big Data and Health Research-The Governance Challenges in a Mixed Data Economy.
Søren Holm, Thomas Ploug. J Bioeth Inq 2017
Søren Holm, Thomas Ploug. J Bioeth Inq 2017
16
Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
5
Finding the missing link for big biomedical data.
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
5
Precision medicine: opportunities, possibilities, and challenges for patients and providers.
Samantha A Adams, Carolyn Petersen. J Am Med Inform Assoc 2016
Samantha A Adams, Carolyn Petersen. J Am Med Inform Assoc 2016
5
A Survey of U.S Adults' Opinions about Conduct of a Nationwide Precision Medicine Initiative® Cohort Study of Genes and Environment.
David J Kaufman, Rebecca Baker, Lauren C Milner, Stephanie Devaney, Kathy L Hudson. PLoS One 2016
David J Kaufman, Rebecca Baker, Lauren C Milner, Stephanie Devaney, Kathy L Hudson. PLoS One 2016
5
The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
5
Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
5
What Is Trust? Ethics and Risk Governance in Precision Medicine and Predictive Analytics.
Afua Adjekum, Marcello Ienca, Effy Vayena. OMICS 2017
Afua Adjekum, Marcello Ienca, Effy Vayena. OMICS 2017
10
Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
7
From public health genomics to precision public health: a 20-year journey.
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
5
A systematic review of barriers to data sharing in public health.
Willem G van Panhuis, Proma Paul, Claudia Emerson, John Grefenstette, Richard Wilder, Abraham J Herbst, David Heymann, Donald S Burke. BMC Public Health 2014
Willem G van Panhuis, Proma Paul, Claudia Emerson, John Grefenstette, Richard Wilder, Abraham J Herbst, David Heymann, Donald S Burke. BMC Public Health 2014
5
Digital health: meeting the ethical and policy challenges.
Effy Vayena, Tobias Haeusermann, Afua Adjekum, Alessandro Blasimme. Swiss Med Wkly 2018
Effy Vayena, Tobias Haeusermann, Afua Adjekum, Alessandro Blasimme. Swiss Med Wkly 2018
5
Rules for processing genetic data for research purposes in view of the new EU General Data Protection Regulation.
Mahsa Shabani, Pascal Borry. Eur J Hum Genet 2018
Mahsa Shabani, Pascal Borry. Eur J Hum Genet 2018
5
From the principles of genomic data sharing to the practices of data access committees.
Mahsa Shabani, Bartha Maria Knoppers, Pascal Borry. EMBO Mol Med 2015
Mahsa Shabani, Bartha Maria Knoppers, Pascal Borry. EMBO Mol Med 2015
7
BBMRI-ERIC Directory: 515 Biobanks with Over 60 Million Biological Samples.
Petr Holub, Morris Swertz, Robert Reihs, David van Enckevort, Heimo Müller, Jan-Eric Litton. Biopreserv Biobank 2016
Petr Holub, Morris Swertz, Robert Reihs, David van Enckevort, Heimo Müller, Jan-Eric Litton. Biopreserv Biobank 2016
5
Framework for responsible sharing of genomic and health-related data.
Bartha Maria Knoppers. Hugo J 2014
Bartha Maria Knoppers. Hugo J 2014
5
Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach.
Menno Mostert, Annelien L Bredenoord, Monique C I H Biesaart, Johannes J M van Delden. Eur J Hum Genet 2016
Menno Mostert, Annelien L Bredenoord, Monique C I H Biesaart, Johannes J M van Delden. Eur J Hum Genet 2016
5
Redefining genomic privacy: trust and empowerment.
Yaniv Erlich, James B Williams, David Glazer, Kenneth Yocum, Nita Farahany, Maynard Olson, Arvind Narayanan, Lincoln D Stein, Jan A Witkowski, Robert C Kain. PLoS Biol 2014
Yaniv Erlich, James B Williams, David Glazer, Kenneth Yocum, Nita Farahany, Maynard Olson, Arvind Narayanan, Lincoln D Stein, Jan A Witkowski, Robert C Kain. PLoS Biol 2014
5
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.