A citation-based method for searching scientific literature

Cindy Chen, Pou-I Lee, Kevin J Pain, Diana Delgado, Curtis L Cole, Thomas R Campion. AMIA Jt Summits Transl Sci Proc 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity



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
25

Health Research with Big Data: Time for Systemic Oversight.
Effy Vayena, Alessandro Blasimme. J Law Med Ethics 2018
31
25

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
25


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
25

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
25


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
25

A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
50
25

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

Prognostic models for identifying risk of poor outcome in people with acute ankle sprains: the SPRAINED development and external validation study.
David J Keene, Michael M Schlüssel, Jacqueline Thompson, Daryl A Hagan, Mark A Williams, Christopher Byrne, Steve Goodacre, Matthew Cooke, Stephen Gwilym, Philip Hormbrey,[...]. Health Technol Assess 2018
2
50

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
25


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
25

The Effect of the General Data Protection Regulation on Medical Research.
John Mark Michael Rumbold, Barbara Pierscionek. J Med Internet Res 2017
41
25

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
25

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
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
25

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
25

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
89
25

User-led research and evidence-based medicine.
Alison Faulkner, Phil Thomas. Br J Psychiatry 2002
92
25


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

Legal issues in governing genetic biobanks: the Italian framework as a case study for the implications for citizen's health through public-private initiatives.
Cinzia Piciocchi, Rossana Ducato, Lucia Martinelli, Silvia Perra, Marta Tomasi, Carla Zuddas, Deborah Mascalzoni. J Community Genet 2018
1
100

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
19
25

Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
95
25

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
25


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
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
25

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
25

The Genetic Family as Patient?
Bartha Maria Knoppers, Kristina Kekesi-Lafrance. Am J Bioeth 2020
4
25

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
25

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
296
25

Data re-identification: societal safeguards.
Russ B Altman, Ellen Wright Clayton, Isaac S Kohane, Bradley A Malin, Dan M Roden. Science 2013
12
25

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
25


Neurobiology of placebo effect in Parkinson's disease: What we have learned and where we are going.
Aldo Quattrone, Gaetano Barbagallo, Antonio Cerasa, A Jon Stoessl. Mov Disord 2018
17
25


Neuro-QOL: brief measures of health-related quality of life for clinical research in neurology.
D Cella, J-S Lai, C J Nowinski, D Victorson, A Peterman, D Miller, F Bethoux, A Heinemann, S Rubin, J E Cavazos,[...]. Neurology 2012
235
25

Placebo response in Parkinson's disease: comparisons among 11 trials covering medical and surgical interventions.
Christopher G Goetz, Joanne Wuu, Michael P McDermott, Charles H Adler, Stanley Fahn, Curt R Freed, Robert A Hauser, Warren C Olanow, Ira Shoulson, P K Tandon,[...]. Mov Disord 2008
177
25

Increasing uncertainty in CNS clinical trials: the role of placebo, nocebo, and Hawthorne effects.
Fabrizio Benedetti, Elisa Carlino, Alessandro Piedimonte. Lancet Neurol 2016
72
25

Impact of placebo assignment in clinical trials of Parkinson's disease.
Christopher G Goetz, Kimberly Janko, Lucy Blasucci, Jean A Jaglin. Mov Disord 2003
25
25

Placebo effect of medication cost in Parkinson disease: a randomized double-blind study.
Alberto J Espay, Matthew M Norris, James C Eliassen, Alok Dwivedi, Matthew S Smith, Christi Banks, Jane B Allendorfer, Anthony E Lang, David E Fleck, Michael J Linke,[...]. Neurology 2015
76
25

What motivates Parkinson's disease patients to enter clinical trials?
Anabela Valadas, Miguel Coelho, Tiago Mestre, Leonor Correia Guedes, Maria Finisterra, Ana Noronha, Mário M Rosa, Cristina Sampaio, Joaquim J Ferreira. Parkinsonism Relat Disord 2011
19
25

Readability of Invasive Procedure Consent Forms.
Adam E M Eltorai, Syed S Naqvi, Soha Ghanian, Craig P Eberson, Arnold-Peter C Weiss, Christopher T Born, Alan H Daniels. Clin Transl Sci 2015
23
25


Association of Electronic Surgical Consent Forms With Entry Error Rates.
J Jeffery Reeves, Kristin L Mekeel, Ruth S Waterman, Lisa R Rhodes, Brian J Clay, Bryan M Clary, Christopher A Longhurst. JAMA Surg 2020
2
50



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.