A citation-based method for searching scientific literature

Megan Prictor, Harriet J A Teare, Jane Kaye.  2018
Times Cited: 15







List of co-cited articles
35 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
211
46

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
119
40

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
40

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
40

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 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
33

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
26

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
159
26

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
26

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
20

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
20

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
20

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
105
20

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
29
20

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
135
20

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
42

Engaging African-Americans about biobanks and the return of research results.
Colin Me Halverson, Lainie Friedman Ross. J Community Genet 2012
32
13

Engaging Māori in biobanking and genomic research: a model for biobanks to guide culturally informed governance, operational, and community engagement activities.
Angela Beaton, Maui Hudson, Moe Milne, Ramari Viola Port, Khyla Russell, Barry Smith, Valmaine Toki, Lynley Uerata, Phillip Wilcox, Karen Bartholomew,[...]. Genet Med 2017
29
13

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

Recall of informed consent information by healthy volunteers in clinical trials.
P Fortun, J West, L Chalkley, A Shonde, C Hawkey. QJM 2008
40
13


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
14

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
35
13

Genuine participation in participant-centred research initiatives: the rhetoric and the potential reality.
Oliver Feeney, Pascal Borry, Heike Felzmann, Lucia Galvagni, Ari Haukkala, Michele Loi, Salvör Nordal, Vojin Rakic, Brígida Riso, Sigrid Sterckx,[...]. J Community Genet 2018
4
50

Human genetic research: emerging trends in ethics.
Bartha Maria Knoppers, Ruth Chadwick. Nat Rev Genet 2005
134
13

Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
49
13

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
51
13


Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples.
Kurt D Christensen, Sarah K Savage, Noelle L Huntington, Elissa R Weitzman, Sonja I Ziniel, Phoebe L Bacon, Cara N Cacioppo, Robert C Green, Ingrid A Holm. J Empir Res Hum Res Ethics 2017
9
22

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
25

Genes, cells, and biobanks: Yes, there's still a consent problem.
Timothy Caulfield, Blake Murdoch. PLoS Biol 2017
34
13

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
178
13

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Cathie Sudlow, John Gallacher, Naomi Allen, Valerie Beral, Paul Burton, John Danesh, Paul Downey, Paul Elliott, Jane Green, Martin Landray,[...]. PLoS Med 2015
13


Biobanking past, present and future: responsibilities and benefits.
Yvonne G De Souza, John S Greenspan. AIDS 2013
107
13


Self-reported race and ethnicity of US biobank participants compared to the US Census.
Elizabeth Gross Cohn, Nalo Hamilton, Elaine L Larson, Janet K Williams. J Community Genet 2017
12
8


Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.
Katrina Armstrong, Ellyn Micco, Amy Carney, Jill Stopfer, Mary Putt. JAMA 2005
282
6

The standardization of race and ethnicity in biomedical science editorials and UK biobanks.
Andrew Smart, Richard Tutton, Paul Martin, George T H Ellison, Richard Ashcroft. Soc Stud Sci 2008
31
6

Pharmacogenomic diversity in Singaporean populations and Europeans.
L R Brunham, S L Chan, R Li, F Aminkeng, X Liu, W Y Saw, R T H Ong, E N Pillai, B C Carleton, D Toh,[...]. Pharmacogenomics J 2014
13
7

Aspects of Modern Biobank Activity - Comprehensive Review.
Wiktor Paskal, Adriana M Paskal, Tomasz Dębski, Maciej Gryziak, Janusz Jaworowski. Pathol Oncol Res 2018
28
6

Australia: public health genomics.
S A Metcalfe, A H Bittles, P O'Leary, J Emery. Public Health Genomics 2009
13
7

Ethical genetic research in Indigenous communities: challenges and successful approaches.
Rebekah E McWhirter, Djapirri Mununggirritj, Dipililnga Marika, Joanne L Dickinson, John R Condon. Trends Mol Med 2012
17
6

The need to build trust: a perspective on disparities in genetic testing.
Kalyn Saulsberry, Sharon F Terry. Genet Test Mol Biomarkers 2013
16
6

Developing and evaluating complex interventions: the new Medical Research Council guidance.
Peter Craig, Paul Dieppe, Sally Macintyre, Susan Michie, Irwin Nazareth, Mark Petticrew. BMJ 2008
6

A review of evidence on consent bias in research.
Khaled El Emam, Elizabeth Jonker, Ester Moher, Luk Arbuckle. Am J Bioeth 2013
14
7


Quality of informed consent: a new measure of understanding among research subjects.
S Joffe, E F Cook, P D Cleary, J W Clark, J C Weeks. J Natl Cancer Inst 2001
245
6



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.