A citation-based method for searching scientific literature

Wylie Burke, Laura M Beskow, Susan Brown Trinidad, Stephanie M Fullerton, Kathleen Brelsford. J Law Med Ethics 2018
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
89
30

Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?
Isabelle Budin-Ljøsne, Deborah Mascalzoni, Sirpa Soini, Helena Machado, Jane Kaye, Heidi Beate Bentzen, Emmanuelle Rial-Sebbag, Flavio D'Abramo, Michał Witt, Geneviève Schamps,[...]. Biopreserv Biobank 2016
13
20

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
296
20

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
115
20

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
89
20

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
203
20

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am J Hum Genet 2015
215
20

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
81
20

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
20

The Common Rule, Updated.
Jerry Menikoff, Julie Kaneshiro, Ivor Pritchard. N Engl J Med 2017
77
20

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
78
20

Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.
Stephanie A Kraft, Mildred K Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E Ormond, Harold S Luft, Benjamin S Wilfond, Sandra Soo-Jin Lee. Am J Bioeth 2018
69
20

Sexual offending runs in families: A 37-year nationwide study.
Niklas Långström, Kelly M Babchishin, Seena Fazel, Paul Lichtenstein, Thomas Frisell. Int J Epidemiol 2015
22
10

Can patient decision aids help people make good decisions about participating in clinical trials? A study protocol.
Jamie C Brehaut, Alison Lott, Dean A Fergusson, Kaveh G Shojania, Jonathan Kimmelman, Raphael Saginur. Implement Sci 2008
17
10


Genetic exceptionalism and legislative pragmatism.
Mark A Rothstein. J Law Med Ethics 2007
17
10

GINA and ADA: New Rule Seriously Dents Previous Protections.
Erin N Oliphant, Sharon F Terry. Genet Test Mol Biomarkers 2016
3
33

Control use of data to protect privacy.
Susan Landau. Science 2015
4
25

Evolving approaches to the ethical management of genomic data.
Jean E McEwen, Joy T Boyer, Kathie Y Sun. Trends Genet 2013
28
10

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
46
10

Informed consent for human genetic and genomic studies: a systematic review.
A Khan, B J Capps, M Y Sum, C N Kuswanto, K Sim. Clin Genet 2014
22
10

NCI think tank concerning the identifiability of biospecimens and "omic" data.
Carol J Weil, Leah E Mechanic, Tiffany Green, Christopher Kinsinger, Nicole C Lockhart, Stefanie A Nelson, Laura L Rodriguez, Laura D Buccini. Genet Med 2013
10
10

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
280
10



Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
167
10

Genetic background of extreme violent behavior.
J Tiihonen, M-R Rautiainen, H M Ollila, E Repo-Tiihonen, M Virkkunen, A Palotie, O Pietiläinen, K Kristiansson, M Joukamaa, H Lauerma,[...]. Mol Psychiatry 2015
63
10

The Affordable Care Act: What's Next?
Mark McClellan, Mark Japinga. Annu Rev Med 2018
2
50

Research ethics. The complexities of genomic identifiability.
Laura L Rodriguez, Lisa D Brooks, Judith H Greenberg, Eric D Green. Science 2013
71
10

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
10


The 21st Century Cures Act - A View from the NIH.
Kathy L Hudson, Francis S Collins. N Engl J Med 2017
48
10


Be prepared for the big genome leak.
Steven E Brenner. Nature 2013
18
10

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
34
10

Population studies: return of research results and incidental findings Policy Statement.
Bartha Maria Knoppers, Mylène Deschênes, Ma'n H Zawati, Anne Marie Tassé. Eur J Hum Genet 2013
72
10


Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
235
10



Using decision aids may improve informed consent for research.
Jamie C Brehaut, Dean A Fergusson, Jonathan Kimmelman, Kaveh G Shojania, Raphael Saginur, Glyn Elwyn. Contemp Clin Trials 2010
26
10

Ethics: Taboo genetics.
Erika Check Hayden. Nature 2013
11
10

Comparative Approaches to Biobanks and Privacy.
Mark A Rothstein, Bartha Maria Knoppers, Heather L Harrell. J Law Med Ethics 2016
15
10


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
799
10




Perceptions of legislation relating to the sharing of genomic biobank results with donors-a survey of BBMRI-ERIC biobanks.
Minna Brunfeldt, Harriet Teare, Sirpa Soini, Helena Kääriäinen. Eur J Hum Genet 2018
3
33



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.