A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


What is a meaningful result? Disclosing the results of genomic research in autism to research participants.
Fiona Alice Miller, Robin Zoe Hayeems, Jessica Peace Bytautas. Eur J Hum Genet 2010
46
44

The emergence of an ethical duty to disclose genetic research results: international perspectives.
Bartha Maria Knoppers, Yann Joly, Jacques Simard, Francine Durocher. Eur J Hum Genet 2006
196
27

One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants.
Fiona Alice Miller, Robin Zoe Hayeems, Li Li, Jessica Peace Bytautas. Eur J Hum Genet 2012
17
29

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
27

Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting.
Conrad V Fernandez, Caron Strahlendorf, Denise Avard, Bartha M Knoppers, Colleen O'Connell, Eric Bouffet, David Malkin, Nada Jabado, Kym Boycott, Poul H Sorensen. Genet Med 2013
36
27

What research participants want to know about genetic research results: the impact of "genetic exceptionalism".
Miguel Ruiz-Canela, J Ignacio Valle-Mansilla, Daniel P Sulmasy. J Empir Res Hum Res Ethics 2011
20
27

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
204
22

When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results.
Fiona A Miller, Mita Giacomini, Catherine Ahern, Jason S Robert, Sonya de Laat. BMC Med Ethics 2008
28
22

Communication of biobanks' research results: what do (potential) participants want?
Tineke M Meulenkamp, Sjef K Gevers, Jasper A Bovenberg, Gerard H Koppelman, Astrid van Hylckama Vlieg, Ellen M A Smets. Am J Med Genet A 2010
66
22

Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results.
Robin Zoe Hayeems, Fiona Alice Miller, Li Li, Jessica Peace Bytautas. Eur J Hum Genet 2011
24
22


Ethics and neuropsychiatric genetics: a review of major issues.
Steven K Hoge, Paul S Appelbaum. Int J Neuropsychopharmacol 2012
23
22

Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy.
Annelien L Bredenoord, N Charlotte Onland-Moret, Johannes J M Van Delden. Hum Mutat 2011
87
22

Disclosure of individual genetic data to research participants: the debate reconsidered.
Annelien L Bredenoord, Hester Y Kroes, Edwin Cuppen, Michael Parker, Johannes J M van Delden. Trends Genet 2011
150
22

Informed consent and genomic incidental findings: IRB chair perspectives.
Christian M Simon, Janet K Williams, Laura Shinkunas, Debra Brandt, Sandra Daack-Hirsch, Martha Driessnack. J Empir Res Hum Res Ethics 2011
35
22


IRB perspectives on the return of individual results from genomic research.
Lynn G Dressler, Sondra Smolek, Roselle Ponsaran, Janell M Markey, Helene Starks, Nancy Gerson, Susan Lewis, Nancy Press, Eric Juengst, Georgia L Wiesner. Genet Med 2012
51
22

Genetic counseling and ethical issues for autism.
William M McMahon, Bonnie Jeanne Baty, Jeffrey Botkin. Am J Med Genet C Semin Med Genet 2006
28
22

Parents' perspectives on participating in genetic research in autism.
Magan Trottier, Wendy Roberts, Irene Drmic, Stephen W Scherer, Rosanna Weksberg, Cheryl Cytrynbaum, David Chitayat, Cheryl Shuman, Fiona A Miller. J Autism Dev Disord 2013
19
22

Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion.
David Kaufman, Gail Geller, Lisa Leroy, Juli Murphy, Joan Scott, Kathy Hudson. Am J Med Genet C Semin Med Genet 2008
60
22

Risk factors for autism: translating genomic discoveries into diagnostics.
Stephen W Scherer, Geraldine Dawson. Hum Genet 2011
76
16

Clinical genetic testing for patients with autism spectrum disorders.
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
243
16


Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
16

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
16

Tailoring the process of informed consent in genetic and genomic research.
Charles N Rotimi, Patricia A Marshall. Genome Med 2010
44
16

Ethical implications of the use of whole genome methods in medical research.
Jane Kaye, Paula Boddington, Jantina de Vries, Naomi Hawkins, Karen Melham. Eur J Hum Genet 2010
59
16

Ethical considerations associated with clinical use of next-generation sequencing in children.
John D Lantos, Michael Artman, Stephen F Kingsmore. J Pediatr 2011
12
25

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
469
16

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
281
16



Ethical issues in psychiatric genetics research: points to consider.
Barbara Bowles Biesecker, Holly Landrum Peay. Psychopharmacology (Berl) 2003
27
16

Research ethics recommendations for whole-genome research: consensus statement.
Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh,[...]. PLoS Biol 2008
156
16

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
159
16

Experiences and attitudes of genome investigators regarding return of individual genetic test results.
Rachel B Ramoni, Amy L McGuire, Jill Oliver Robinson, Debra S Morley, Sharon E Plon, Steven Joffe. Genet Med 2013
39
16

Public perspectives on returning genetics and genomics research results.
J O'Daniel, S B Haga. Public Health Genomics 2011
57
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

Researcher practices on returning genetic research results.
Christopher Heaney, Genevieve Tindall, Joe Lucas, Susanne B Haga. Genet Test Mol Biomarkers 2010
25
16


Disclosing individual CDKN2A research results to melanoma survivors: interest, impact, and demands on researchers.
Kurt D Christensen, J Scott Roberts, David I Shalowitz, Jessica N Everett, Scott Y H Kim, Leon Raskin, Stephen B Gruber. Cancer Epidemiol Biomarkers Prev 2011
38
16

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
56
16


Public preferences for the return of research results in genetic research: a conjoint analysis.
Juli Murphy Bollinger, John F P Bridges, Ateesha Mohamed, David Kaufman. Genet Med 2014
36
16


Parent perspectives on pediatric genetic research and implications for genotype-driven research recruitment.
Holly K Tabor, Tracy Brazg, Julia Crouch, Emily E Namey, Stephanie M Fullerton, Laura M Beskow, Benjamin S Wilfond. J Empir Res Hum Res Ethics 2011
37
16

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013
124
16

Attitudes of stakeholders in psychiatry towards the inclusion of children in genomic research.
Anna Sundby, Merete Watt Boolsen, Kristoffer Sølvsten Burgdorf, Henrik Ullum, Thomas Folkmann Hansen, Ole Mors. Hum Genomics 2018
10
30

Communication of pharmacogenetic research results to HIV-infected treated patients: standpoints of professionals and patients.
Grégoire Moutel, Nathalie Duchange, François Raffi, Lama I Sharara, Ioannis Théodorou, Violaine Noël, Sandrine de Montgolfier, Ingrid Callies, François Bricaire, Christian Hervé,[...]. Eur J Hum Genet 2005
24
11



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.