A citation-based method for searching scientific literature

Elena Salvaterra, Roberto Giorda, Maria T Bassi, Renato Borgatti, Lisbeth E Knudsen, Andrea Martinuzzi, Maria Nobile, Uberto Pozzoli, Gian P Ramelli, Gianl L Reni, Damiano Rivolta, Maria A Stazi, Sandra Strazzer, Carel Thijs, Virgilia Toccaceli, Antonio Trabacca, Anna C Turconi, Sergio Zanini, Claudio Zucca, Nereo Bresolin, Leonardo Lenzi On Behalf Of The Pediatric Biobank Elsi Working Group. Biopreserv Biobank 2012
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


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
37

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
45
37

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
31

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

Translational research in pediatrics: tissue sampling and biobanking.
Alayne R Brisson, Doreen Matsui, Michael J Rieder, Douglas D Fraser. Pediatrics 2012
49
31

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
132
31

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

Risks, benefits, solidarity: a framework for the participation of children in genetic biobank research.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. J Pediatr 2011
14
28

Research ethics. Children and population biobanks.
David Gurwitz, Isabel Fortier, Jeantine E Lunshof, Bartha Maria Knoppers. Science 2009
59
25

Children, longitudinal studies, and informed consent.
Gert Helgesson. Med Health Care Philos 2005
20
25

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
25

Opinions of children about participation in medical genetic research.
S van der Pal, B Sozanska, D Madden, A Kosmeda, A Debinska, H Danielewicz, A Boznanski, S Detmar. Public Health Genomics 2011
10
40



Ethics in studies on children and environmental health.
D F Merlo, L E Knudsen, K Matusiewicz, L Niebrój, K H Vähäkangas. J Med Ethics 2007
24
25

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
306
25

Researchers' opinions towards the communication of results of biobank research: a survey study.
Tineke M Meulenkamp, Sjef J K Gevers, Jasper A Bovenberg, Ellen M A Smets. Eur J Hum Genet 2012
13
30

Clarifying assent in pediatric research.
Noor A A Giesbertz, Annelien L Bredenoord, Johannes J M van Delden. Eur J Hum Genet 2014
26
25

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
18

Ethics and biobanks.
M G Hansson. Br J Cancer 2009
107
18


The return of individual research findings in paediatric genetic research.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. J Med Ethics 2011
48
18

Child assent and parental permission in pediatric research.
Wilma C Rossi, William Reynolds, Robert M Nelson. Theor Med Bioeth 2003
56
18

Consent and research governance in biobanks: evidence from focus groups with medical researchers.
E A Whitley, N Kanellopoulou, J Kaye. Public Health Genomics 2012
27
18



Consent procedures in pediatric biobanks.
Noor Aa Giesbertz, Annelien L Bredenoord, Johannes Jm van Delden. Eur J Hum Genet 2015
13
23

Engaging African-Americans about biobanks and the return of research results.
Colin Me Halverson, Lainie Friedman Ross. J Community Genet 2012
34
18

"Still Rather Hazy at Present": Citizens' and Physicians' Views on Returning Results from Biobank Research Using Broad Consent.
Gaia Barazzetti, Samuele Cavalli, Lazare Benaroyo, Alain Kaufmann. Genet Test Mol Biomarkers 2017
7
42

The development of a preference-setting model for the return of individual genomic research results.
Phoebe L Bacon, Erin D Harris, Sonja I Ziniel, Sarah K Savage, Elissa R Weitzman, Robert C Green, Noelle L Huntington, Ingrid A Holm. J Empir Res Hum Res Ethics 2015
17
18

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
209
18



Ethics of future disclosure of individual risk information in a genetic cohort study: a survey of donor preferences.
Kenji Matsui, Reidar K Lie, Yoshikuni Kita, Hirotsugu Ueshima. J Epidemiol 2008
21
12

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
474
12



Biobanks: oversight offers protection.
Kristien Hens, John Wright, Kris Dierickx. Science 2009
15
13

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
153
12

Biobanks: too long to wait for consent.
Kyle B Brothers, Ellen Wright Clayton. Science 2009
17
12

Storage policies and use of the Danish Newborn Screening Biobank.
B Nørgaard-Pedersen, D M Hougaard. J Inherit Metab Dis 2007
156
12

Do Illustrations Improve Children's Comprehension of Assent Documents?
Kim G Adcock, Shirley M Hogan, Okan U Elci, Keri L Mills. J Pediatr Pharmacol Ther 2012
5
40

Ethical issues related to biomonitoring studies on children.
Marie Pedersen, Domenico Franco Merlo, Lisbeth E Knudsen. Int J Hyg Environ Health 2007
8
25


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
12


Assent in pediatric research.
Alexander A Kon. Pediatrics 2006
26
12





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.