A citation-based method for searching scientific literature


List of co-cited articles
11 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
230
50

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
126
50


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
92
37

Informed consent within a learning health system: A scoping review.
Annabelle Cumyn, Adrien Barton, Roxanne Dault, Anne-Marie Cloutier, Rosalie Jalbert, Jean-François Ethier. Learn Health Syst 2019
7
42

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
146
25

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
34
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
56
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
11
25

Patient Perspectives on the Learning Health System: The Importance of Trust and Shared Decision Making.
Maureen Kelley, Cyan James, Stephanie Alessi Kraft, Diane Korngiebel, Isabelle Wijangco, Emily Rosenthal, Steven Joffe, Mildred K Cho, Benjamin Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2015
51
25

Patient and Physician Views about Protocolized Dialysis Treatment in Randomized Trials and Clinical Care.
Ashley Kraybill, Laura M Dember, Steven Joffe, Jason Karlawish, Susan S Ellenberg, Vanessa Madden, Scott D Halpern. AJOB Empir Bioeth 2016
14
25

23andMe: a new two-sided data-banking market model.
Henri-Corto Stoeklé, Marie-France Mamzer-Bruneel, Guillaume Vogt, Christian Hervé. BMC Med Ethics 2016
30
12

[Toward dynamic informed consent].
Henri-Corto Stoeklé, Jean-François Deleuze, Guillaume Vogt, Christian Hervé. Med Sci (Paris) 2017
6
16

The rise and fall and rise again of 23andMe.
Erika Check Hayden. Nature 2017
17
12


Molecular Tumor Boards: Ethical Issues in the New Era of Data Medicine.
Henri-Corto Stoeklé, Marie-France Mamzer-Bruneel, Charles-Henry Frouart, Christophe Le Tourneau, Pierre Laurent-Puig, Guillaume Vogt, Christian Hervé. Sci Eng Ethics 2018
15
12

[The Jardé law, a real simplification of research in France?]
C Levy, A Rybak, R Cohen, C Jung. Arch Pediatr 2017
3
33

[Genetic data sharing: a new type of capital].
Henri-Corto Stoeklé, Ninon Forster, Philippe Charlier, Oudy C Bloch, Christian Hervé, Mauro Turrini, Guillaume Vogt. Med Sci (Paris) 2018
6
16





Broadening consent--and diluting ethics?
B Hofmann. J Med Ethics 2009
97
12

In defense of broad consent.
Gert Helgesson. Camb Q Healthc Ethics 2012
42
12

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
232
12

Adopting clinical genomics: a systematic review of genomic literacy among physicians in cancer care.
Vu T Dung Ha, Julie Frizzo-Barker, Peter Chow-White. BMC Med Genomics 2018
21
12


Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
474
12


Glad you asked: participants' opinions of re-consent for dbGap data submission.
Evette J Ludman, Stephanie M Fullerton, Leslie Spangler, Susan Brown Trinidad, Monica M Fujii, Gail P Jarvik, Eric B Larson, Wylie Burke. J Empir Res Hum Res Ethics 2010
84
12

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
902
12

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
162
12


Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
481
12

Precision medicine: the foundation of future cancer therapeutics.
Seung Ho Shin, Ann M Bode, Zigang Dong. NPJ Precis Oncol 2017
47
12

Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?
Edward S Dove, Vicky Chico, Michael Fay, Graeme Laurie, Anneke M Lucassen, Emily Postan. J Med Ethics 2019
16
12

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019
20
12

Can I access my personal genome? The current legal position in the UK.
Jane Kaye, Nadja Kanellopoulou, Naomi Hawkins, Heather Gowans, Liam Curren, Karen Melham. Med Law Rev 2014
15
12

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.
Daniele Carrieri, Heidi C Howard, Caroline Benjamin, Angus J Clarke, Sandi Dheensa, Shane Doheny, Naomi Hawkins, Tanya F Halbersma-Konings, Leigh Jackson, Hülya Kayserili,[...]. Eur J Hum Genet 2019
38
12

Patient-centric trials for therapeutic development in precision oncology.
Andrew V Biankin, Steven Piantadosi, Simon J Hollingsworth. Nature 2015
165
12

Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalpé, Bartha Maria Knoppers. Eur J Hum Genet 2019
42
12

Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature.
Alma Husedzinovic, Dominik Ose, Christoph Schickhardt, Stefan Fröhling, Eva C Winkler. Eur J Hum Genet 2015
30
12

Attitudes of patients with cancer about personalized medicine and somatic genetic testing.
Stacy W Gray, Katherine Hicks-Courant, Christopher S Lathan, Levi Garraway, Elyse R Park, Jane C Weeks. J Oncol Pract 2012
82
12

Do patients and research subjects have a right to receive their genomic raw data? An ethical and legal analysis.
Christoph Schickhardt, Henrike Fleischer, Eva C Winkler. BMC Med Ethics 2020
7
14


The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Yvonne Bombard, Kyle B Brothers, Sara Fitzgerald-Butt, Nanibaa' A Garrison, Leila Jamal, Cynthia A James, Gail P Jarvik, Jennifer B McCormick, Tanya N Nelson, Kelly E Ormond,[...]. Am J Hum Genet 2019
55
12

Potential research participants support the return of raw sequence data.
Anna Middleton, Caroline F Wright, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Michael Parker. J Med Genet 2015
27
12

Personal privacy, public benefits, and biobanks: a conjoint analysis of policy priorities and public perceptions.
Daryl Pullman, Holly Etchegary, Katherine Gallagher, Kathleen Hodgkinson, Montgomery Keough, David Morgan, Catherine Street. Genet Med 2012
35
12


So rare we need to hunt for them: reframing the ethical debate on incidental findings.
Sebastian Schuol, Christoph Schickhardt, Stefan Wiemann, Claus R Bartram, Klaus Tanner, Roland Eils, Benjamin Meder, Daniela Richter, Hanno Glimm, Christof von Kalle,[...]. Genome Med 2015
9
12


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.