A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Ignorance, information and autonomy.
J Harris, K Keywood. Theor Med Bioeth 2001
47
100



INTRODUCTION: From the Right to Know to the Right Not to Know.
Bartha Maria Knoppers. J Law Med Ethics 2014
14
75





Genetic information, rights, and autonomy.
M Häyry, T Takala. Theor Med Bioeth 2001
20
50

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
50

"Please don't tell me". The right not to know.
Jonathan Herring, Charles Foster. Camb Q Healthc Ethics 2012
16
50



The right not to know: the case of psychiatric disorders.
Lisa Bortolotti, Heather Widdows. J Med Ethics 2011
24
50

Homo Ignorans: Deliberately Choosing Not to Know.
Ralph Hertwig, Christoph Engel. Perspect Psychol Sci 2016
15
50

The 'right' not to know.
D E Ost. J Med Philos 1984
32
50

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
118
25

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
207
25

Moral Duties of Genomics Researchers: Why Personalized Medicine Requires a Collective Approach.
Shoko Vos, Johannes J M van Delden, Paul J van Diest, Annelien L Bredenoord. Trends Genet 2017
12
25

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
831
25

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
120
25

Assessing Genetic Literacy Awareness and Knowledge Gaps in the US Population: Results from the Health Information National Trends Survey.
Melinda Krakow, Chelsea L Ratcliff, Bradford W Hesse, Alexandra J Greenberg-Worisek. Public Health Genomics 2017
26
25

Methods of data collection in qualitative research: interviews and focus groups.
P Gill, K Stewart, E Treasure, B Chadwick. Br Dent J 2008
354
25

Clinical genetic counselors: An asset in the era of precision medicine.
Catherine A L Wicklund, Debra A Duquette, Amy L Swanson. Am J Med Genet C Semin Med Genet 2018
8
25

Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland).
Anna Middleton, Chris Patch, Jennifer Wiggins, Kathy Barnes, Gill Crawford, Caroline Benjamin, Anita Bruce. Eur J Hum Genet 2014
20
25

The Right to Know: A Revised Standard for Reporting Incidental Findings.
G Owen Schaefer, Julian Savulescu. Hastings Cent Rep 2018
10
25




Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur J Hum Genet 2016
234
25


Points to consider for laboratories reporting results from diagnostic genomic sequencing.
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur J Hum Genet 2018
29
25

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.
Jonathan S Berg, Laura M Amendola, Christine Eng, Eliezer Van Allen, Stacy W Gray, Nikhil Wagle, Heidi L Rehm, Elizabeth T DeChene, Matthew C Dulik, Fuki M Hisama,[...]. Genet Med 2013
88
25


A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet Med 2017
48
25

Medical decision making: paternalism versus patient-centered (autonomous) care.
Carlos A Rodriguez-Osorio, Guillermo Dominguez-Cherit. Curr Opin Crit Care 2008
58
25


Shared decision making, paternalism and patient choice.
Lars Sandman, Christian Munthe. Health Care Anal 2010
103
25


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
25

Is It Our Duty To Hunt for Pathogenic Mutations?
Roel H P Wouters, Rhodé M Bijlsma, Geert W J Frederix, Margreet G E M Ausems, Johannes J M van Delden, Emile E Voest, Annelien L Bredenoord. Trends Mol Med 2018
4
25

Reporting genomic secondary findings: ACMG members weigh in.
Maren T Scheuner, Jane Peredo, Judith Benkendorf, Bruce Bowdish, Gerald Feldman, Lynn Fleisher, John J Mulvihill, Michael Watson, Gail E Herman, James Evans. Genet Med 2015
36
25

"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
37
25

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
213
25

Disclosing incidental findings in genetics contexts: a review of the empirical ethical research.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Med Genet 2013
29
25


Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
71
25


Genetic ignorance and reasonable paternalism.
T Takala. Theor Med Bioeth 2001
17
25


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.