-
2
-
-
84939273999
-
-
Council of Europe, Committee of Ministers: Recommendation Rec(2006)4 of the Committee of Ministers to Member States on Research on Biological Materials of Human Origin. Strasbourg: Council of Europe, 2006
-
Council of Europe, Committee of Ministers: Recommendation Rec(2006)4 of the Committee of Ministers to Member States on Research on Biological Materials of Human Origin. Strasbourg: Council of Europe, 2006.
-
-
-
-
3
-
-
33745672350
-
Genetics U.S. Hospital launches large biobank of children's DNA
-
Kaiser J: Genetics. U.S. hospital launches large biobank of children's DNA. Science 2006; 312: 1584-1585.
-
(2006)
Science
, vol.312
, pp. 1584-1585
-
-
Kaiser, J.1
-
4
-
-
31544478017
-
Genetics Biobank ties cancer genes to rare developmental syndrome
-
Vogel G: Genetics. Biobank ties cancer genes to rare developmental syndrome. Science 2006; 311: 456.
-
(2006)
Science
, vol.311
, pp. 456
-
-
Vogel, G.1
-
5
-
-
84855290932
-
Translational research in pediatrics: Tissue sampling and biobanking
-
Brisson AR, Matsui D, Rieder MJ, Fraser DD: Translational research in pediatrics: tissue sampling and biobanking. Pediatrics 2012; 129: 153-162.
-
(2012)
Pediatrics
, vol.129
, pp. 153-162
-
-
Brisson, A.R.1
Matsui, D.2
Rieder, M.J.3
Fraser, D.D.4
-
6
-
-
84856923860
-
Pediatric biobanking: A pilot qualitative survey of practices, rules, and researcher opinions in ten European Countries
-
Salvaterra E, Giorda R, Bassi MT, et al: Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European Countries. Biopreserv Biobank 2012; 10: 29-36.
-
(2012)
Biopreserv Biobank
, vol.10
, pp. 29-36
-
-
Salvaterra, E.1
Giorda, R.2
Bassi, M.T.3
-
7
-
-
84953437016
-
Biobanking in pediatric research
-
Hutton J (ed) Dordrecht, Netherlands: Springer
-
Barnes MG, Lynch JA, Corsmo JJ, Witte DP, Steele PE: Biobanking in pediatric research; in Hutton J (ed): Pediatric Biomedical Informatics. Computer Applications in Pediatric Research. Dordrecht, Netherlands: Springer, 2012, Vol 2, pp 109-129.
-
(2012)
Pediatric Biomedical Informatics Computer Applications in Pediatric Research
, vol.2
, pp. 109-129
-
-
Barnes, M.G.1
Lynch, J.A.2
Corsmo, J.J.3
Witte, D.P.4
Steele, P.E.5
-
8
-
-
84888372656
-
Recurrent H3.3 alterations in childhood tumors
-
Lindroth AM, Plass C: Recurrent H3.3 alterations in childhood tumors. Nat Genet 2013; 45: 1413-1414.
-
(2013)
Nat Genet
, vol.45
, pp. 1413-1414
-
-
Lindroth, A.M.1
Plass, C.2
-
11
-
-
79954417226
-
Risks, benefits, solidarity: A framework for the participation of children in genetic biobank research
-
Hens K, Nys H, Cassiman JJ, Dierickx K: Risks, benefits, solidarity: a framework for the participation of children in genetic biobank research. J Pediatr 2011; 158: 842-848.
-
(2011)
J Pediatr
, vol.158
, pp. 842-848
-
-
Hens, K.1
Nys, H.2
Cassiman, J.J.3
Dierickx, K.4
-
12
-
-
0027571658
-
Minors' assent, consent, or dissent to medical research
-
Leikin S: Minors' assent, consent, or dissent to medical research. IRB 1993; 15: 1-7.
-
(1993)
IRB
, vol.15
, pp. 1-7
-
-
Leikin, S.1
-
14
-
-
84939266875
-
-
US Department of Health and Human Services (HHS): Human Subject Research (45 CFR 46, Subpart D). Washington, DC: HHS
-
US Department of Health and Human Services (HHS): Human Subject Research (45 CFR 46, Subpart D). Protections for Children involved as Subjects in Research. Washington, DC: HHS, 2009.
-
(2009)
Protections for Children Involved As Subjects in Research
-
-
-
16
-
-
67749109823
-
Biological sample collections from minors for genetic research: A systematic review of guidelines and position papers
-
Hens K, Nys H, Cassiman JJ, Dierickx K: Biological sample collections from minors for genetic research: a systematic review of guidelines and position papers. Eur J Hum Genet 2009; 17: 979-990.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 979-990
-
-
Hens, K.1
Nys, H.2
Cassiman, J.J.3
Dierickx, K.4
-
17
-
-
84871185661
-
Developing a policy for paediatric biobanks: Principles for good practice
-
Hens K, Van El CE, Borry P, et al: Developing a policy for paediatric biobanks: principles for good practice. Eur J Hum Genet 2013; 21: 2-7.
-
(2013)
Eur J Hum Genet
, vol.21
, pp. 2-7
-
-
Hens, K.1
Van El, C.E.2
Borry, P.3
-
18
-
-
79960147836
-
Opinions of children about participation in medical genetic research
-
van der Pal S, Sozanska B, Madden D, et al: Opinions of children about participation in medical genetic research. Public Health Genom 2011; 14: 271-278.
-
(2011)
Public Health Genom
, vol.14
, pp. 271-278
-
-
Van Der Pal, S.1
Sozanska, B.2
Madden, D.3
-
19
-
-
84855562709
-
My parents decide if i can i decide if i want to. Children's views on participation in medical research
-
Swartling U, Hansson MG, Ludvigsson J, Nordgren A: My parents decide if I can. I decide if I want to. Children's views on participation in medical research. J Empir Res Hum Res Ethics 2011; 6: 68-75.
-
(2011)
J Empir Res Hum Res Ethics
, vol.6
, pp. 68-75
-
-
Swartling, U.1
Hansson, M.G.2
Ludvigsson, J.3
Nordgren, A.4
-
20
-
-
79952448540
-
The storage and use of biological tissue samples from minors for research: A focus group study
-
Hens K, Nys H, Cassiman JJ, Dierickx K: The storage and use of biological tissue samples from minors for research: a focus group study. Public Health Genomics 2011; 14: 68-76.
-
(2011)
Public Health Genomics
, vol.14
, pp. 68-76
-
-
Hens, K.1
Nys, H.2
Cassiman, J.J.3
Dierickx, K.4
-
21
-
-
77951571382
-
Handling ethical, legal and social issues in birth cohort studies involving genetic research: Responses from studies in six countries
-
Ries NM, LeGrandeur J, Caulfield T: Handling ethical, legal and social issues in birth cohort studies involving genetic research: responses from studies in six countries. BMC Med Ethics 2010; 11: 4.
-
(2010)
BMC Med Ethics
, vol.11
, pp. 4
-
-
Ries, N.M.1
LeGrandeur, J.2
Caulfield, T.3
-
22
-
-
84873025492
-
Emerging issues in paediatric health research consent forms in Canada: Working towards best practices
-
Dove ES, Avard D, Black L, Knoppers BM: Emerging issues in paediatric health research consent forms in Canada: working towards best practices. BMC Med Ethics 2013; 14: 5.
-
(2013)
BMC Med Ethics
, vol.14
, pp. 5
-
-
Dove, E.S.1
Avard, D.2
Black, L.3
Knoppers, B.M.4
-
23
-
-
0029562599
-
Genetic research, adolescents, and informed consent
-
Weir RF, Horton JR: Genetic research, adolescents, and informed consent. Theor Med 1995; 16: 347-373.
-
(1995)
Theor Med
, vol.16
, pp. 347-373
-
-
Weir, R.F.1
Horton, J.R.2
-
24
-
-
84906823390
-
Introduction: How to know whether and when to use case studies as a research method
-
Yin RK (ed) Thousand Oaks, CA, USA: Sage Publications
-
Yin RK: Introduction: how to know whether and when to use case studies as a research method; in Yin RK (ed): Case Study Research: Design and Methods, 4th edn. Thousand Oaks, CA, USA: Sage Publications, 2009, Vol 5, pp 3-23.
-
(2009)
Case Study Research: Design and Methods, 4th Edn
, vol.5
, pp. 3-23
-
-
Yin, R.K.1
-
25
-
-
38349132543
-
Universal risk factors for multifactorial diseases: LifeLines: A three-generation population-based study
-
Stolk RP, Rosmalen JG, Postma DS, et al: Universal risk factors for multifactorial diseases: LifeLines: a three-generation population-based study. Eur J Epidemiol 2008; 23: 67-74.
-
(2008)
Eur J Epidemiol
, vol.23
, pp. 67-74
-
-
Stolk, R.P.1
Rosmalen, J.G.2
Postma, D.S.3
-
26
-
-
84899894644
-
Cohort profile: The prevention and incidence of asthma and mite allergy (PIAMA) birth cohort
-
Wijga AH, Kerkhof M, Gehring U, et al: Cohort profile: The Prevention and Incidence of Asthma and Mite Allergy (PIAMA) birth cohort. Int J Epidemiol 2014; 43: 527-535.
-
(2014)
Int J Epidemiol
, vol.43
, pp. 527-535
-
-
Wijga, A.H.1
Kerkhof, M.2
Gehring, U.3
-
27
-
-
84899875829
-
Cohort profile of the Young-HUNT Study, Norway: A population-based study of adolescents
-
Holmen TL, Bratberg G, Krokstad S, et al: Cohort profile of the Young-HUNT Study, Norway: a population-based study of adolescents. Int J Epidemiol 2014; 43: 539-544.
-
(2014)
Int J Epidemiol
, vol.43
, pp. 539-544
-
-
Holmen, T.L.1
Bratberg, G.2
Krokstad, S.3
-
28
-
-
35648962168
-
Analyzing case study evidence: How to tart your analysis, your analytic choices, and how they work
-
Yin RK (ed) Thousand Oaks, CA, USA: Sage Publictions
-
Yin RK: Analyzing case study evidence: how to tart your analysis, your analytic choices, and how they work; in Yin RK (ed): Case Study Research: Design and Methods, 4th edn. Thousand Oaks, CA, USA: Sage Publictions, 2009, Vol 5, pp 127-163.
-
(2009)
Case Study Research: Design and Methods, 4th Edn
, vol.5
, pp. 127-163
-
-
Yin, R.K.1
-
29
-
-
84939274000
-
-
NVivo qualitative data analysis [computer program] Version 10. QSR International Pty Ltd, 2012
-
NVivo qualitative data analysis [computer program] Version 10. QSR International Pty Ltd, 2012.
-
-
-
-
30
-
-
84939274001
-
-
Wet Medisch Wetenschappelijk Onderzoek met Mensen Article 6. [Medical Research involving Human Beings], Revised (last accessed 9 December 2013)
-
Wet Medisch Wetenschappelijk Onderzoek met Mensen Article 6. [Medical Research involving Human Beings], Revised 2012. Available at: http://wetten.overheid.nl/ BWBR0009408/geldigheidsdatum-09-12-2013 (last accessed 9 December 2013).
-
(2012)
-
-
-
31
-
-
84939274002
-
-
Human Tissue Act. Chapter 30. Part 1 Section 2(last accessed 9 December 2013)
-
Human Tissue Act. Chapter 30. Part 1 Section 2. 2004. Available at: http://www. legislation.gov.uk/ukpga/2004/30/section/2 (last accessed 9 December 2013).
-
(2004)
-
-
-
32
-
-
84939274003
-
-
Lov om medisinsk og helsefaglig forskning (helseforskningsloven), Chapter 4, 17 and 18. [the Health Research Act], Revised (last accessed 12 December 2013)
-
Lov om medisinsk og helsefaglig forskning (helseforskningsloven), Chapter 4, 17 and 18. [the Health Research Act], Revised 2013. Available at: http://lovdata.no/dokument/ NL/lov/2008-06-20-44 (last accessed 12 December 2013).
-
(2013)
-
-
-
33
-
-
84939274004
-
-
Lov om pasient-og brukerrettigheter (pasient-og brukerrettighetsloven), 4.4 [the Patient's Rights Act], Revised (last ccessed 12 December 2013)
-
Lov om pasient-og brukerrettigheter (pasient-og brukerrettighetsloven), 4.4 [the Patient's Rights Act], Revised 2011. Available at: http://lovdata.no/dokument/NL/lov/ 1999-07-02-63 (last ccessed 12 December 2013).
-
(2011)
-
-
-
34
-
-
84939274005
-
-
Human Tissue Authority. Code of practice 1: Consent. Updated (last accessed 3 September 2014)
-
Human Tissue Authority. Code of practice 1: Consent. Updated 2014. Available at: http://www.hta.gov.uk/-db/-documents/Code-of-practice-1-Consent.pdf (last accessed 3 September 2014).
-
(2014)
-
-
-
35
-
-
84939274006
-
-
Medical Research Council. Research and the Human Tissue Act-Consent. MRC Regulatory Support Centre (last accessed 3 September 2014)
-
Medical Research Council. Research and the Human Tissue Act-Consent. MRC Regulatory Support Centre 2007. Available at: http://www.mrc.ac.uk/research/ facilities/regulatory-support-centre/human-tissue/related-content/consent-summary/ (last accessed 3 September 2014).
-
(2007)
-
-
-
36
-
-
33847122440
-
Consent for childhood cancer tissue banking in the UK: The effect of the Human Tissue Act 2004
-
McHale J, Habiba M, Dixon-Woods M, Cavers D, Heney D, Pritchard-Jones K: Consent for childhood cancer tissue banking in the UK: the effect of the Human Tissue Act 2004. Lancet Oncol 2007; 8: 266-272.
-
(2007)
Lancet Oncol
, vol.8
, pp. 266-272
-
-
McHale, J.1
Habiba, M.2
Dixon-Woods, M.3
Cavers, D.4
Heney, D.5
Pritchard-Jones, K.6
-
38
-
-
79952417119
-
Biobanks need publicity
-
Gaskell G, Gottweis H: Biobanks need publicity. Nature 2011; 471: 159-160.
-
(2011)
Nature
, vol.471
, pp. 159-160
-
-
Gaskell, G.1
Gottweis, H.2
-
39
-
-
85190208402
-
-
Oxford, UK: Hart Publishing Limited
-
Kaye J, Gibbons SMC, Heeney C, Parker M, Smart A: Governing Biobanks: Understanding the Interplay Between Law And Practice, 1 edn. Oxford, UK: Hart Publishing Limited, 2012.
-
(2012)
Governing Biobanks: Understanding the Interplay between Law and Practice, 1 Edn
-
-
Kaye, J.1
Gibbons, S.M.C.2
Heeney, C.3
Parker, M.4
Smart, A.5
-
40
-
-
2442506800
-
Governing UK Biobank: The importance of ensuring public trust
-
Tutton R, Kaye J, Hoeyer K: Governing UK Biobank: the importance of ensuring public trust. Trends Biotechnol 2004; 22: 284-285.
-
(2004)
Trends Biotechnol
, vol.22
, pp. 284-285
-
-
Tutton, R.1
Kaye, J.2
Hoeyer, K.3
-
41
-
-
80054983939
-
Research ethics: Treat donors as partners in biobank research
-
Saha K, Hurlbut JB: Research ethics: treat donors as partners in biobank research. Nature 2011; 478: 312-313.
-
(2011)
Nature
, vol.478
, pp. 312-313
-
-
Saha, K.1
Hurlbut, J.B.2
-
42
-
-
84939274007
-
-
United Nations New York, NY, USA: United Nations
-
United Nations: Convention on the Rights of the Child. New York, NY, USA: United Nations, 1989.
-
(1989)
Convention on the Rights of the Child
-
-
-
44
-
-
84909970242
-
-
European Commision. Biobanks for Europe Luxembourg: Expert Group on Dealing with Ethical and Regulatory Challenges of International Biobank Research, European Union
-
European Commision. Biobanks for Europe: A Challenge For Governance. Luxembourg: Expert Group on Dealing with Ethical and Regulatory Challenges of International Biobank Research, European Union, 2012.
-
(2012)
A Challenge for Governance
-
-
|