A citation-based method for searching scientific literature

Jennifer Klima, Sara M Fitzgerald-Butt, Kelly J Kelleher, Deena J Chisolm, R Dawn Comstock, Amy K Ferketich, Kim L McBride. Genet Med 2014
Times Cited: 38







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



Times Cited
  Times     Co-cited
Similarity


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
108
23

Children, biobanks and the scope of parental consent.
Kristien Hens, Jean-Jacques Cassiman, Herman Nys, Kris Dierickx. Eur J Hum Genet 2011
35
25

Research ethics. Children and population biobanks.
David Gurwitz, Isabel Fortier, Jeantine E Lunshof, Bartha Maria Knoppers. Science 2009
59
18

Children and biobanks: a review of the ethical and legal discussion.
Kristien Hens, Emmanuelle Lévesque, Kris Dierickx. Hum Genet 2011
31
22

Opinions of Adolescents and Parents About Pediatric Biobanking.
Cynthia C Kong, Tamsin E Tarling, Caron Strahlendorf, Michelle Dittrick, Suzanne M Vercauteren. J Adolesc Health 2016
15
46

Developing a policy for paediatric biobanks: principles for good practice.
Kristien Hens, Carla E Van El, Pascal Borry, Anne Cambon-Thomsen, Martina C Cornel, Francesca Forzano, Anneke Lucassen, Christine Patch, Lisbeth Tranebjaerg, Eric Vermeulen,[...]. Eur J Hum Genet 2013
46
15

Translational research in pediatrics: tissue sampling and biobanking.
Alayne R Brisson, Doreen Matsui, Michael J Rieder, Douglas D Fraser. Pediatrics 2012
50
15

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
20

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
59
13

Paediatric biobanks: what makes them so unique?
Julie Samuël, Bartha M Knoppers, Denise Avard. J Paediatr Child Health 2012
14
35

Informed consent: how much and what do patients understand?
Matthew E Falagas, Ioanna P Korbila, Konstantina P Giannopoulou, Barbara K Kondilis, George Peppas. Am J Surg 2009
185
13

Quality of informed consent: a new measure of understanding among research subjects.
S Joffe, E F Cook, P D Cleary, J W Clark, J C Weeks. J Natl Cancer Inst 2001
257
13

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
10

Parental Perspectives on a Pediatric Human Non-Subjects Biobank.
Kyle B Brothers, Ellen Wright Clayton. AJOB Prim Res 2012
20
20

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
44
10

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
10

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
53
10

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
10

Factors influencing parental consent in pediatric clinical research.
Justin D Rothmier, Mary V Lasley, Gail G Shapiro. Pediatrics 2003
86
10

Opinions of Young Adults on Re-Consenting for Biobanking.
Amanda Rush, Robert Battisti, Belinda Barton, Daniel Catchpoole. J Pediatr 2015
12
33

Factors influencing public participation in biobanking.
Mamoun Ahram, Areej Othman, Manal Shahrouri, Ebtihal Mustafa. Eur J Hum Genet 2014
46
10

Characterizing biobank organizations in the U.S.: results from a national survey.
Gail E Henderson, R Jean Cadigan, Teresa P Edwards, Ian Conlon, Anders G Nelson, James P Evans, Arlene M Davis, Catherine Zimmer, Bryan J Weiner. Genome Med 2013
136
10

Participant understanding and recall of informed consent for induced pluripotent stem cell biobanking.
Tristan McCaughey, Christine Y Chen, Elisabeth De Smit, Gwyneth Rees, Eva Fenwick, Lisa S Kearns, David A Mackey, Casimir MacGregor, Megan Munsie, Anthony L Cook,[...]. Cell Tissue Bank 2016
14
28


A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
61
7

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
218
7


Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
99
7



The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository.
Erin D Harris, Sonja I Ziniel, Jonathan G Amatruda, Catherine M Clinton, Sarah K Savage, Patrick L Taylor, Noelle L Huntington, Robert C Green, Ingrid A Holm. Genet Med 2012
39
7

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
177
7

Emerging issues in paediatric health research consent forms in Canada: working towards best practices.
Edward S Dove, Denise Avard, Lee Black, Bartha M Knoppers. BMC Med Ethics 2013
14
21

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
33
9



Empirical data about women's attitudes toward a biobank focused on pregnancy outcomes.
Josh W Joseph, Alon B Neidich, Carole Ober, Lainie Friedman Ross. Am J Med Genet A 2008
29
10


Pediatric data sharing in genomic research: attitudes and preferences of parents.
Matthew D Burstein, Jill Oliver Robinson, Susan G Hilsenbeck, Amy L McGuire, Ching C Lau. Pediatrics 2014
23
13

Glad you asked: participants' opinions of re-consent for dbGap data submission.
Evette J Ludman, Stephanie M Fullerton, Leslie Spangler, Susan Brown Trinidad, Monica M Fujii, Gail P Jarvik, Eric B Larson, Wylie Burke. J Empir Res Hum Res Ethics 2010
86
7

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
56
7

False hopes and best data: consent to research and the therapeutic misconception.
P S Appelbaum, L H Roth, C W Lidz, P Benson, W Winslade. Hastings Cent Rep 1987
573
7

Factors that influence parental decisions to participate in clinical research: consenters vs nonconsenters.
Alejandro Hoberman, Nader Shaikh, Sonika Bhatnagar, Mary Ann Haralam, Diana H Kearney, D Kathleen Colborn, Michelle L Kienholz, Li Wang, Clareann H Bunker, Ron Keren,[...]. JAMA Pediatr 2013
74
7

Perception of risk associated with asthma research procedures among adolescents, parents, and pediatricians.
Robert D Annett, Janet L Brody, David G Scherer, Elizabeth A Perkett. J Allergy Clin Immunol 2004
18
16


Comparisons of adolescent and parent willingness to participate in minimal and above-minimal risk pediatric asthma research protocols.
Janet L Brody, Robert D Annett, David G Scherer, Mandy L Perryman, Keely M W Cofrin. J Adolesc Health 2005
63
7

The therapeutic misconception: problems and solutions.
Charles W Lidz, Paul S Appelbaum. Med Care 2002
169
7


Consent for biobanking: assessing the understanding and views of cancer patients.
Julien Mancini, Isabelle Pellegrini, Frédéric Viret, Norbert Vey, Lise-Marie Daufresne, Christian Chabannon, Claire Julian-Reynier. J Natl Cancer Inst 2011
22
13

Participants' recall and understanding of genomic research and large-scale data sharing.
Jill Oliver Robinson, Melody J Slashinski, Tao Wang, Susan G Hilsenbeck, Amy L McGuire. J Empir Res Hum Res Ethics 2013
34
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.