A citation-based method for searching scientific literature

Victoria Coathup, Harriet J A Teare, Jusaku Minari, Go Yoshizawa, Jane Kaye, Masanori P Takahashi, Kazuto Kato. BMC Med Ethics 2016
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


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
157
35

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
133
35

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
208
35

Towards 'Engagement 2.0': Insights from a study of dynamic consent with biobank participants.
Harriet Ja Teare, Michael Morrison, Edgar A Whitley, Jane Kaye. Digit Health 2015
23
28

The Cooperative Health Research in South Tyrol (CHRIS) study: rationale, objectives, and preliminary results.
Cristian Pattaro, Martin Gögele, Deborah Mascalzoni, Roberto Melotti, Christine Schwienbacher, Alessandro De Grandi, Luisa Foco, Yuri D'Elia, Barbara Linder, Christian Fuchsberger,[...]. J Transl Med 2015
28
28

The RUDY study platform - a novel approach to patient driven research in rare musculoskeletal diseases.
M K Javaid, L Forestier-Zhang, L Watts, A Turner, C Ponte, H Teare, D Gray, N Gray, R Popert, J Hogg,[...]. Orphanet J Rare Dis 2016
22
28

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
76
28

The evolution of withdrawal: negotiating research relationships in biobanking.
Karen Melham, Linda Briceno Moraia, Colin Mitchell, Michael Morrison, Harriet Teare, Jane Kaye. Life Sci Soc Policy 2014
9
33

Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
117
21

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
21

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
21

Patient Perspectives on Sharing Anonymized Personal Health Data Using a Digital System for Dynamic Consent and Research Feedback: A Qualitative Study.
Karen Spencer, Caroline Sanders, Edgar A Whitley, David Lund, Jane Kaye, William Gregory Dixon. J Med Internet Res 2016
62
21

Participant-Centric Initiatives: Tools to Facilitate Engagement In Research.
Nicholas Anderson, Caleb Bragg, Andrea Hartzler, Kelly Edwards. Appl Transl Genom 2012
21
21

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
54
21

Scoping studies: advancing the methodology.
Danielle Levac, Heather Colquhoun, Kelly K O'Brien. Implement Sci 2010
21

Patient engagement in research: a systematic review.
Juan Pablo Domecq, Gabriela Prutsky, Tarig Elraiyah, Zhen Wang, Mohammed Nabhan, Nathan Shippee, Juan Pablo Brito, Kasey Boehmer, Rim Hasan, Belal Firwana,[...]. BMC Health Serv Res 2014
624
21

The emerging need for family-centric initiatives for obtaining consent in personal genome research.
Jusaku Minari, Harriet Teare, Colin Mitchell, Jane Kaye, Kazuto Kato. Genome Med 2014
12
25

The RUDY study: using digital technologies to enable a research partnership.
Harriet J A Teare, Joanna Hogg, Jane Kaye, Raashid Luqmani, Elaine Rush, Alison Turner, Laura Watts, Melanie Williams, M Kassim Javaid. Eur J Hum Genet 2017
18
21

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
34
21

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
14

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
49
14

A dynamic model of patient consent to sharing of medical record data.
William G Dixon, Karen Spencer, Hawys Williams, Caroline Sanders, David Lund, Edgar A Whitley, Jane Kaye. BMJ 2014
10
20

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
26
14

Improving the recruitment activity of clinicians in randomised controlled trials: a systematic review.
Ben Fletcher, Adrian Gheorghe, David Moore, Sue Wilson, Sarah Damery. BMJ Open 2012
182
14

Challenges of web-based personal genomic data sharing.
Mahsa Shabani, Pascal Borry. Life Sci Soc Policy 2015
12
16

First, design for data sharing.
John Wilbanks, Stephen H Friend. Nat Biotechnol 2016
26
14

Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials.
Adam Nishimura, Jantey Carey, Patricia J Erwin, Jon C Tilburt, M Hassan Murad, Jennifer B McCormick. BMC Med Ethics 2013
225
14

Patient and family engagement: a framework for understanding the elements and developing interventions and policies.
Kristin L Carman, Pam Dardess, Maureen Maurer, Shoshanna Sofaer, Karen Adams, Christine Bechtel, Jennifer Sweeney. Health Aff (Millwood) 2013
637
14


The experiential knowledge of patients: a new resource for biomedical research?
J Francisca Caron-Flinterman, Jacqueline E W Broerse, Joske F G Bunders. Soc Sci Med 2005
151
14

Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond.
Go Yoshizawa, Teguh H Sasongko, Chih-Hsing Ho, Kazuto Kato. Front Genet 2017
5
40

Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents.
Nchangwi Syntia Munung, Patricia Marshall, Megan Campbell, Katherine Littler, Francis Masiye, Odile Ouwe-Missi-Oukem-Boyer, Janet Seeley, D J Stein, Paulina Tindana, Jantina de Vries. J Med Ethics 2016
30
14

Patient Portals and Patient Engagement: A State of the Science Review.
Taya Irizarry, Annette DeVito Dabbs, Christine R Curran. J Med Internet Res 2015
299
14

Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
31
14



Measuring quality of life impairment in skeletal muscle channelopathies.
V A Sansone, C Ricci, M Montanari, G Apolone, M Rose, G Meola. Eur J Neurol 2012
39
14

Validation of The Individualized Neuromuscular Quality of Life in Japanese patients with myotonic dystrophy.
Haruo Fujino, Toshio Saito, Masanori P Takahashi, Hiroto Takada, Takahiro Nakayama, Katsuhisa Ogata, Michael R Rose, Osamu Imura, Tsuyoshi Matsumura. Muscle Nerve 2018
3
66

Construction and validation of a quality of life questionnaire for neuromuscular disease (INQoL).
K A Vincent, A J Carr, J Walburn, D L Scott, M R Rose. Neurology 2007
92
14

FUNCTIONAL EVALUATION: THE BARTHEL INDEX.
F I MAHONEY, D W BARTHEL. Md State Med J 1965
14

Translation, adaptation, and validation of the SF-36 Health Survey for use in Japan.
S Fukuhara, S Bito, J Green, A Hsiao, K Kurokawa. J Clin Epidemiol 1998
807
14


If you build it, they will come: unintended future uses of organised health data collections.
Kieran C O'Doherty, Emily Christofides, Jeffery Yen, Heidi Beate Bentzen, Wylie Burke, Nina Hallowell, Barbara A Koenig, Donald J Willison. BMC Med Ethics 2016
19
7

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
78
7

Medicine. The NIH Roadmap.
Elias Zerhouni. Science 2003
586
7


Opening up to precompetitive collaboration.
Jill S Altshuler, Erin Balogh, Anna D Barker, Stephen L Eck, Stephen H Friend, Geoffrey S Ginsburg, Roy S Herbst, Sharyl J Nass, Christopher M Streeter, John A Wagner. Sci Transl Med 2010
39
7

Personal genomes: Misdirected precaution.
Barbara Prainsack, Jenny Reardon, Richard Hindmarsh, Herbert Gottweis, Ursula Naue, Jeantine E Lunshof. Nature 2008
60
7

Challenges and opportunities for ELSI early career researchers.
Jessica Bell, Mirko Ancillotti, Victoria Coathup, Sarah Coy, Tessel Rigter, Travis Tatum, Jasjote Grewal, Faruk Berat Akcesme, Jovana Brkić, Anida Causevic-Ramosevac,[...]. BMC Med Ethics 2016
4
25

Research priorities. ELSI 2.0 for genomics and society.
Jane Kaye, Eric M Meslin, Bartha M Knoppers, Eric T Juengst, Mylène Deschênes, Anne Cambon-Thomsen, Donald Chalmers, Jantina De Vries, Kelly Edwards, Nils Hoppe,[...]. Science 2012
24
7


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.