A citation-based method for searching scientific literature

Jusaku Minari, Harriet Teare, Colin Mitchell, Jane Kaye, Kazuto Kato. Genome Med 2014
Times Cited: 12







List of co-cited articles
42 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
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
33


A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
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
119
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
135
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
81
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 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
29
25

Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
50
16

Genetics patients' perspectives on clinical genomic testing.
Michelle L McGowan, Allison Glinka, Janelle Highland, George Asaad, Richard R Sharp. Per Med 2013
29
16

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
16

Informed consent for biobanking: consensus-based guidelines for adequate comprehension.
Laura M Beskow, Carrie B Dombeck, Cole P Thompson, J Kemp Watson-Ormond, Kevin P Weinfurt. Genet Med 2015
38
16

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
232
16


Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
46
16

Quality of informed consent in cancer clinical trials: a cross-sectional survey.
S Joffe, E F Cook, P D Cleary, J W Clark, J C Weeks. Lancet 2001
413
16

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
466
16

The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
124
16

GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N Engl J Med 2015
97
16


The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.
Gail E Henderson, Susan M Wolf, Kristine J Kuczynski, Steven Joffe, Richard R Sharp, D Williams Parsons, Bartha M Knoppers, Joon-Ho Yu, Paul S Appelbaum. J Law Med Ethics 2014
47
16

Informed consent in genomics and genetic research.
Amy L McGuire, Laura M Beskow. Annu Rev Genomics Hum Genet 2010
92
16


Tissue donation to biobanks: a review of sociological studies.
Wendy Lipworth, Rowena Forsyth, Ian Kerridge. Sociol Health Illn 2011
36
16


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
228
16



Informed consent in the genomics era.
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
56
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
159
16

For what am I participating? The need for communication after receiving consent from biobanking project participants: experience in Japan.
Maiko Watanabe, Yusuke Inoue, Chiungfang Chang, Hyunsoo Hong, Izumi Kobayashi, Satoshi Suzuki, Kaori Muto. J Hum Genet 2011
18
16

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
16

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
52
16

Genetic discrimination: international perspectives.
M Otlowski, S Taylor, Y Bombard. Annu Rev Genomics Hum Genet 2012
64
16

ELSI practices in genomic research in East Asia: implications for research collaboration and public participation.
Go Yoshizawa, Calvin Wai-Loon Ho, Wei Zhu, Chingli Hu, Yoni Syukriani, Ilhak Lee, Hannah Kim, Daniel Fu Chang Tsai, Jusaku Minari, Kazuto Kato. Genome Med 2014
13
16

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

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

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
16

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
534
16

A developmental approach to child assent for nontherapeutic research.
Victoria A Miller, Robert M Nelson. J Pediatr 2006
37
8

Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.
Christopher H Wade, Beth A Tarini, Benjamin S Wilfond. Annu Rev Genomics Hum Genet 2013
42
8

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
798
8

Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
Angela R Bradbury, Linda Patrick-Miller, Jessica Long, Jacquelyn Powers, Jill Stopfer, Andrea Forman, Christina Rybak, Kristin Mattie, Amanda Brandt, Rachelle Chambers,[...]. Genet Med 2015
53
8

Resistance to therapy in acute promyelocytic leukemia.
Jacqueline Lehmann-Che, Cecile Bally, Hugues de Thé. N Engl J Med 2014
76
8

Teaching genomic counseling: preparing the genetic counseling workforce for the genomic era.
Gillian W Hooker, Kelly E Ormond, Kevin Sweet, Barbara B Biesecker. J Genet Couns 2014
45
8




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.