A citation-based method for searching scientific literature

Clair Morrissey, Rebecca L Walker. J Med Philos 2018
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


Ignorance, information and autonomy.
J Harris, K Keywood. Theor Med Bioeth 2001
49
50


Genetic information, rights, and autonomy.
M Häyry, T Takala. Theor Med Bioeth 2001
20
37



The 'right' not to know.
D E Ost. J Med Philos 1984
33
37

The promise and peril of genomic screening in the general population.
Michael C Adams, James P Evans, Gail E Henderson, Jonathan S Berg. Genet Med 2016
38
25

Population genetic testing for cancer susceptibility: founder mutations to genomes.
William D Foulkes, Bartha Maria Knoppers, Clare Turnbull. Nat Rev Clin Oncol 2016
63
25





Rethinking the 'right not to know'.
Rosalind McDougall. Monash Bioeth Rev 2004
5
40

Genetic Moralism and Health.
Tuija Takala. Camb Q Healthc Ethics 2019
4
50

The right not to know HIV-test results.
M Temmerman, J Ndinya-Achola, J Ambani, P Piot. Lancet 1995
160
25

"Please don't tell me". The right not to know.
Jonathan Herring, Charles Foster. Camb Q Healthc Ethics 2012
16
25


INTRODUCTION: From the Right to Know to the Right Not to Know.
Bartha Maria Knoppers. J Law Med Ethics 2014
15
25

The right not to know: the case of psychiatric disorders.
Lisa Bortolotti, Heather Widdows. J Med Ethics 2011
25
25

Homo Ignorans: Deliberately Choosing Not to Know.
Ralph Hertwig, Christoph Engel. Perspect Psychol Sci 2016
18
25


The right to genetic ignorance confirmed.
Tuija Takala. Bioethics 1999
31
25

Have we seen the geneticisation of society? Expectations and evidence.
Kate Weiner, Paul Martin, Martin Richards, Richard Tutton. Sociol Health Illn 2017
11
25

Standards for reporting qualitative research: a synthesis of recommendations.
Bridget C O'Brien, Ilene B Harris, Thomas J Beckman, Darcy A Reed, David A Cook. Acad Med 2014
25

Does personalized melanoma genomic risk information trigger conversations about skin cancer prevention and skin examination with family, friends and health professionals?
A K Smit, L A Keogh, A J Newson, P N Butow, K Dunlop, R L Morton, J Kirk, D Espinoza, A E Cust. Br J Dermatol 2017
13
25

The role of non-directiveness in genetic counseling.
Fuat S Oduncu. Med Health Care Philos 2002
23
25

A Pilot Randomized Controlled Trial of the Feasibility, Acceptability, and Impact of Giving Information on Personalized Genomic Risk of Melanoma to the Public.
Amelia K Smit, David Espinoza, Ainsley J Newson, Rachael L Morton, Georgina Fenton, Lucinda Freeman, Kate Dunlop, Phyllis N Butow, Matthew H Law, Michael G Kimlin,[...]. Cancer Epidemiol Biomarkers Prev 2017
29
25


A response to "Personalised medicine and population health: breast and ovarian cancer".
Antonis Antoniou, Hoda Anton-Culver, Alexander Borowsky, Mireille Broeders, Jennifer Brooks, Anna Chiarelli, Jocelyne Chiquette, Jack Cuzick, Suzette Delaloge, Peter Devilee,[...]. Hum Genet 2019
10
25

Attitudes to incorporating genomic risk assessments into population screening programs: the importance of purpose, context and deliberation.
Stuart G Nicholls, Holly Etchegary, June C Carroll, David Castle, Louise Lemyre, Beth K Potter, Samantha Craigie, Brenda J Wilson. BMC Med Genomics 2016
10
25


Cancer genetics, precision prevention and a call to action.
Clare Turnbull, Amit Sud, Richard S Houlston. Nat Genet 2018
49
25

Reconciling Opportunistic and Population Screening in Clinical Genomics.
Kyle B Brothers, Jason L Vassy, Robert C Green. Mayo Clin Proc 2019
13
25

Precision Public Health for the Era of Precision Medicine.
Muin J Khoury, Michael F Iademarco, William T Riley. Am J Prev Med 2016
219
25

Reconceptualizing Autonomy for Bioethics.
Lisa Dive, Ainsley J Newson. Kennedy Inst Ethics J 2018
10
25

How to get older people included in clinical studies.
Miles D Witham, Marion E T McMurdo. Drugs Aging 2007
64
12

Upper age limits in studies submitted to a research ethics committee.
Alfonso J Cruz-Jentoft, Begoña Gutiérrez. Aging Clin Exp Res 2010
10
12

Addressing the ethical challenges in genetic testing and sequencing of children.
Ellen Wright Clayton, Laurence B McCullough, Leslie G Biesecker, Steven Joffe, Lainie Friedman Ross, Susan M Wolf. Am J Bioeth 2014
71
12

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
12

We screen newborns, don't we?: realizing the promise of public health genomics.
James P Evans, Jonathan S Berg, Andrew F Olshan, Terry Magnuson, Barbara K Rimer. Genet Med 2013
44
12

Population screening in the age of genomic medicine.
Muin J Khoury, Linda L McCabe, Edward R B McCabe. N Engl J Med 2003
244
12

Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Marcia Van Riper, Rebecca L Walker, Eric T Juengst. Am J Bioeth 2015
28
12

Attitudes towards personal genomics among older Swiss adults: An exploratory study.
Laura Mählmann, Christina Röcke, Angela Brand, Ernst Hafen, Effy Vayena. Appl Transl Genom 2016
11
12

Online Education and e-Consent for GeneScreen, a Preventive Genomic Screening Study.
R Jean Cadigan, Rita Butterfield, Christine Rini, Margaret Waltz, Kristine J Kuczynski, Kristin Muessig, Katrina A B Goddard, Gail E Henderson. Public Health Genomics 2017
11
12

Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
212
12

The persistent exclusion of older patients from ongoing clinical trials regarding heart failure.
Antonio Cherubini, Joaquim Oristrell, Xavier Pla, Carmelinda Ruggiero, Roberta Ferretti, Germán Diestre, A Mark Clarfield, Peter Crome, Cees Hertogh, Vita Lesauskaite,[...]. Arch Intern Med 2011
186
12

Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement.
Kirsten Bibbins-Domingo, David C Grossman, Susan J Curry, Karina W Davidson, John W Epling, Francisco A R García, Matthew W Gillman, Diane M Harper, Alex R Kemper, Alex H Krist,[...]. JAMA 2016
12

Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
259
12

Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?
Anya E R Prince, John M Conley, Arlene M Davis, Gabriel Lázaro-Muñoz, R Jean Cadigan. J Law Med Ethics 2015
9
12

Population-based screening for BRCA1 and BRCA2: 2014 Lasker Award.
Mary-Claire King, Ephrat Levy-Lahad, Amnon Lahad. JAMA 2014
174
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.