A citation-based method for searching scientific literature

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
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
44

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
33

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
27

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
27

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
27

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
22

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
22

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
22


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

Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan.
Victoria Coathup, Harriet J A Teare, Jusaku Minari, Go Yoshizawa, Jane Kaye, Masanori P Takahashi, Kazuto Kato. BMC Med Ethics 2016
14
21

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
16

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
16

Authority and the Future of Consent in Population-Level Biomedical Research.
Mark Sheehan, Rachel Thompson, Jon Fistein, Jim Davies, Michael Dunn, Michael Parker, Julian Savulescu, Kerrie Woods. Public Health Ethics 2019
8
37


The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
122
11

GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledge.
Brianne E Kirkpatrick, Erin Rooney Riggs, Danielle R Azzariti, Vanessa Rangel Miller, David H Ledbetter, David T Miller, Heidi Rehm, Christa Lese Martin, W Andrew Faucett. Hum Mutat 2015
39
11

Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population.
Anna Fry, Thomas J Littlejohns, Cathie Sudlow, Nicola Doherty, Ligia Adamska, Tim Sprosen, Rory Collins, Naomi E Allen. Am J Epidemiol 2017
603
11

The "vampire project".
B J Crigger. Hastings Cent Rep 1995
3
66

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
518
11

Communicating with biobank participants: preferences for receiving and providing updates to researchers.
Jessica L Mester, MaryBeth Mercer, Aaron Goldenberg, Rebekah A Moore, Charis Eng, Richard R Sharp. Cancer Epidemiol Biomarkers Prev 2015
8
25

Genes, cells, and biobanks: Yes, there's still a consent problem.
Timothy Caulfield, Blake Murdoch. PLoS Biol 2017
34
11

'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research.
Pauline McCormack, Anna Kole, Sabina Gainotti, Deborah Mascalzoni, Caron Molster, Hanns Lochmüller, Simon Woods. Eur J Hum Genet 2016
35
11

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
22

Participants' recall and understanding of genomic research and large-scale data sharing.
Jill Oliver Robinson, Melody J Slashinski, Tao Wang, Susan G Hilsenbeck, Amy L McGuire. J Empir Res Hum Res Ethics 2013
29
11

Recall of informed consent information by healthy volunteers in clinical trials.
P Fortun, J West, L Chalkley, A Shonde, C Hawkey. QJM 2008
40
11

Standards for reporting qualitative research: a synthesis of recommendations.
Bridget C O'Brien, Ilene B Harris, Thomas J Beckman, Darcy A Reed, David A Cook. Acad Med 2014
11


Participant-Centric Initiatives: Tools to Facilitate Engagement In Research.
Nicholas Anderson, Caleb Bragg, Andrea Hartzler, Kelly Edwards. Appl Transl Genom 2012
21
11

Patient and Other Stakeholder Engagement in Patient-Centered Outcomes Research Institute Funded Studies of Patients with Kidney Diseases.
Daniel Cukor, Lewis M Cohen, Elizabeth L Cope, Nasrollah Ghahramani, S Susan Hedayati, Denise M Hynes, Vallabh O Shah, Francesca Tentori, Mark Unruh, Jeanette Bobelu,[...]. Clin J Am Soc Nephrol 2016
35
11

Advocacy groups as research organizations: the PXE International example.
Sharon F Terry, Patrick F Terry, Katherine A Rauen, Jouni Uitto, Lionel G Bercovitch. Nat Rev Genet 2007
95
11

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
11

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
11


Dynamic Consent: An Evaluation and Reporting Framework.
Megan Prictor, Megan A Lewis, Ainsley J Newson, Matilda Haas, Sachiko Baba, Hannah Kim, Minori Kokado, Jusaku Minari, Fruzsina Molnár-Gábor, Beverley Yamamoto,[...]. J Empir Res Hum Res Ethics 2020
7
28

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
11

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
11



Trust, trustworthiness and sharing patient data for research.
Mark Sheehan, Phoebe Friesen, Adrian Balmer, Corina Cheeks, Sara Davidson, James Devereux, Douglas Findlay, Katharine Keats-Rohan, Rob Lawrence, Kamran Shafiq. J Med Ethics 2020
6
33


Distinguishing research from clinical care in cancer genetics: theoretical justifications and practical strategies.
Nina Hallowell, Sarah Cooke, Gill Crawford, Anneke Lucassen, Michael Parker. Soc Sci Med 2009
30
5


An investigation of patients' motivations for their participation in genetics-related research.
N Hallowell, S Cooke, G Crawford, A Lucassen, M Parker, C Snowdon. J Med Ethics 2010
66
5

Enterprising or altruistic selves? Making up research subjects in genetics research.
Richard Tutton, Barbara Prainsack. Sociol Health Illn 2011
20
5



Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach.
Gabrielle Natalie Samuel, Sandi Dheensa, Bobbie Farsides, Angela Fenwick, Anneke Lucassen. BMC Med Ethics 2017
22
5


An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
266
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.