A citation-based method for searching scientific literature

David Kaufman, Gail Geller, Lisa Leroy, Juli Murphy, Joan Scott, Kathy Hudson. Am J Med Genet C Semin Med Genet 2008
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity


Research ethics. Children and population biobanks.
David Gurwitz, Isabel Fortier, Jeantine E Lunshof, Bartha Maria Knoppers. Science 2009
59
28

Genetic research on stored tissue samples from minors: a systematic review of the ethical literature.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. Am J Med Genet A 2009
34
47

Empirical data about women's attitudes towards a hypothetical pediatric biobank.
Alon B Neidich, Josh W Joseph, Carole Ober, Lainie Friedman Ross. Am J Med Genet A 2008
45
31

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
210
23


Biological sample collections from minors for genetic research: a systematic review of guidelines and position papers.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. Eur J Hum Genet 2009
34
38

Pediatric biobanks: approaching informed consent for continuing research after children grow up.
Aaron J Goldenberg, Sara Chandros Hull, Jeffrey R Botkin, Benjamin S Wilfond. J Pediatr 2009
52
23

The storage and use of biological tissue samples from minors for research: a focus group study.
K Hens, H Nys, J-J Cassiman, K Dierickx. Public Health Genomics 2011
29
41



Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
140
15

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
198
15

Patients' views on identifiability of samples and informed consent for genetic research.
Sara Chandros Hull, Richard R Sharp, Jeffrey R Botkin, Mark Brown, Mark Hughes, Jeremy Sugarman, Debra Schwinn, Pamela Sankar, Dragana Bolcic-Jankovic, Brian R Clarridge,[...]. Am J Bioeth 2008
81
13

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
163
13

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
477
13

The return of individual research findings in paediatric genetic research.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. J Med Ethics 2011
48
16

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
182
13

Informed consent and biobanks.
Ellen Wright Clayton. J Law Med Ethics 2005
58
12


Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.
Ebony B Bookman, Aleisha A Langehorne, John H Eckfeldt, Kathleen C Glass, Gail P Jarvik, Michael Klag, Greg Koski, Arno Motulsky, Benjamin Wilfond, Teri A Manolio,[...]. Am J Med Genet A 2006
162
11

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
223
11

Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
232
11


Children, longitudinal studies, and informed consent.
Gert Helgesson. Med Health Care Philos 2005
20
35

Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
86
11

Biobanks: oversight offers protection.
Kristien Hens, John Wright, Kris Dierickx. Science 2009
15
46

Researchers' perceptions of the ethical implications of pharmacogenomics research with children.
D Avard, T Silverstein, G Sillon, Y Joly. Public Health Genomics 2009
23
30

Children, biobanks and the scope of parental consent.
Kristien Hens, Jean-Jacques Cassiman, Herman Nys, Kris Dierickx. Eur J Hum Genet 2011
35
20

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
286
11




Science and society: children and incompetent adults in genetic research: consent and safeguards.
Bartha Maria Knoppers, Denise Avard, Geneviève Cardinal, Kathleen Cranley Glass. Nat Rev Genet 2002
29
20





Children's consent to research participation: social context and personal experience invalidate fixed cutoff rules.
Richard Ashcroft, Trudy Goodenough, Emma Williamson, Julie Kent. Am J Bioeth 2003
17
35



Assessing the understanding of biobank participants.
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
107
10

Public and biobank participant attitudes toward genetic research participation and data sharing.
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
176
10

Children and biobanks: a review of the ethical and legal discussion.
Kristien Hens, Emmanuelle Lévesque, Kris Dierickx. Hum Genet 2011
31
19



Development of a large-scale de-identified DNA biobank to enable personalized medicine.
D M Roden, J M Pulley, M A Basford, G R Bernard, E W Clayton, J R Balser, D R Masys. Clin Pharmacol Ther 2008
574
8

Attitudes and perceptions of patients towards methods of establishing a DNA biobank.
Jill M Pulley, Margaret M Brace, Gordon R Bernard, Dan R Masys. Cell Tissue Bank 2008
75
8

The return of research results to participants: pilot questionnaire of adolescents and parents of children with cancer.
C V Fernandez, D Santor, C Weijer, C Strahlendorf, A Moghrabi, R Pentz, J Gao, E Kodish. Pediatr Blood Cancer 2007
51
9

Informed consent for population-based research involving genetics.
L M Beskow, W Burke, J F Merz, P A Barr, S Terry, V B Penchaszadeh, L O Gostin, M Gwinn, M J Khoury. JAMA 2001
185
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.