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


Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
8

Leading the way to genomic medicine.
Teri A Manolio, Eric D Green. Am J Med Genet C Semin Med Genet 2014
20
8


Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
72
8

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
58
8

The new genetics and informed consent: differentiating choice to preserve autonomy.
Eline M Bunnik, Antina de Jong, Niels Nijsingh, Guido M W R de Wert. Bioethics 2013
37
8

The invisible hand in clinical research: the study coordinator's critical role in human subjects protection.
Arlene M Davis, Sara Chandros Hull, Christine Grady, Benjamin S Wilfond, Gail E Henderson. J Law Med Ethics 2002
51
8



Return of results: ethical and legal distinctions between research and clinical care.
Wylie Burke, Barbara J Evans, Gail P Jarvik. Am J Med Genet C Semin Med Genet 2014
71
8



What keeps you up at night? Genetics professionals' distressing experiences in patient care.
Barbara A Bernhardt, Rachel Silver, Cynda Hylton Rushton, Ellyn Micco, Gail Geller. Genet Med 2010
19
8

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
216
8

Precision medicine: Beyond the inflection point.
Sam Hawgood, India G Hook-Barnard, Theresa C O'Brien, Keith R Yamamoto. Sci Transl Med 2015
59
8

Power to the people: a wiki-governance model for biobanks.
Edward S Dove, Yann Joly, Bartha M Knoppers. Genome Biol 2012
24
8


Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
23
8

Health data cooperatives - citizen empowerment.
E Hafen, D Kossmann, A Brand. Methods Inf Med 2014
47
8

Genomics and privacy: implications of the new reality of closed data for the field.
Dov Greenbaum, Andrea Sboner, Xinmeng Jasmine Mu, Mark Gerstein. PLoS Comput Biol 2011
37
8

The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat Biotechnol 2015
115
8


Finding the missing link for big biomedical data.
Griffin M Weber, Kenneth D Mandl, Isaac S Kohane. JAMA 2014
167
8

Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.
J M Oliver, M J Slashinski, T Wang, P A Kelly, S G Hilsenbeck, A L McGuire. Public Health Genomics 2012
70
8

A public resource facilitating clinical use of genomes.
Madeleine P Ball, Joseph V Thakuria, Alexander Wait Zaranek, Tom Clegg, Abraham M Rosenbaum, Xiaodi Wu, Misha Angrist, Jong Bhak, Jason Bobe, Matthew J Callow,[...]. Proc Natl Acad Sci U S A 2012
118
8

Getting human rights right in global health policy.
John Tasioulas, Effy Vayena. Lancet 2015
6
16


Research participants' attitudes towards the confidentiality of genomic sequence information.
Leila Jamal, Julie C Sapp, Katie Lewis, Tatiane Yanes, Flavia M Facio, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2014
28
8

The charitable trust as a model for genomic biobanks.
David E Winickoff, Richard N Winickoff. N Engl J Med 2003
102
8

Redefining genomic privacy: trust and empowerment.
Yaniv Erlich, James B Williams, David Glazer, Kenneth Yocum, Nita Farahany, Maynard Olson, Arvind Narayanan, Lincoln D Stein, Jan A Witkowski, Robert C Kain. PLoS Biol 2014
50
8

Routes for breaching and protecting genetic privacy.
Yaniv Erlich, Arvind Narayanan. Nat Rev Genet 2014
138
8

The need to redefine genomic data sharing: A focus on data accessibility.
Tempest A van Schaik, Nadezda V Kovalevskaya, Elena Protopapas, Hamza Wahid, Fiona G G Nielsen. Appl Transl Genom 2014
12
8

Genomic data in the electronic medical record: perspectives from a biobank community advisory board.
Brittany C Kimball, Katherine E Nowakowski, Karen J Maschke, Jennifer B McCormick. J Empir Res Hum Res Ethics 2014
18
8

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
8

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Jason L Vassy, Denise M Lautenbach, Heather M McLaughlin, Sek Won Kong, Kurt D Christensen, Joel Krier, Isaac S Kohane, Lindsay Z Feuerman, Jennifer Blumenthal-Barby, J Scott Roberts,[...]. Trials 2014
102
8


Communicating genetic risk information for common disorders in the era of genomic medicine.
Denise M Lautenbach, Kurt D Christensen, Jeffrey A Sparks, Robert C Green. Annu Rev Genomics Hum Genet 2013
83
8

Validation of a decision regret scale.
Jamie C Brehaut, Annette M O'Connor, Timothy J Wood, Thomas F Hack, Laura Siminoff, Elisa Gordon, Deb Feldman-Stewart. Med Decis Making 2003
603
8

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.
Leslie G Biesecker, James C Mullikin, Flavia M Facio, Clesson Turner, Praveen F Cherukuri, Robert W Blakesley, Gerard G Bouffard, Peter S Chines, Pedro Cruz, Nancy F Hansen,[...]. Genome Res 2009
203
8

Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing.
Angela R Bradbury, Linda J Patrick-Miller, Brian L Egleston, Laura DiGiovanni, Jamie Brower, Diana Harris, Evelyn M Stevens, Kara N Maxwell, Abha Kulkarni, Tyler Chavez,[...]. Genet Med 2016
43
8

Meeting the governance challenges of next-generation biorepository research.
Stephanie M Fullerton, Nicholas R Anderson, Greg Guzauskas, Dena Freeman, Kelly Fryer-Edwards. Sci Transl Med 2010
47
8

Research ethics. Research practice and participant preferences: the growing gulf.
S B Trinidad, S M Fullerton, E J Ludman, G P Jarvik, E B Larson, W Burke. Science 2011
67
8

Informed consent: a broken contract.
Erika Check Hayden. Nature 2012
30
8


Bringing the Common Rule into the 21st Century.
Kathy L Hudson, Francis S Collins. N Engl J Med 2015
45
8


Developing a simplified consent form for biobanking.
Laura M Beskow, Joëlle Y Friedman, N Chantelle Hardy, Li Lin, Kevin P Weinfurt. PLoS One 2010
60
8

Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
123
8

Custodianship as an ethical framework for biospecimen-based research.
Rihab Yassin, Nicole Lockhart, Mariana González del Riego, Karen Pitt, Jeffrey W Thomas, Linda Weiss, Carolyn Compton. Cancer Epidemiol Biomarkers Prev 2010
33
8

Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
84
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.