UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Direct-to-consumer genetic testing: Prospective users' attitudes toward information about ancestry and biological relationships

PloS one, 2021-11, Vol.16 (11), p.e0260340-e0260340

2021

Volltextzugriff (PDF)

Thought leader perspectives on benefits and harms in precision medicine research

PloS one, 2018-11, Vol.13 (11), p.e0207842-e0207842

2018

Volltextzugriff (PDF)

The lived experience of prostate cancer: 10-year survivor perspectives following contemporary treatment of localized prostate cancer

Journal of cancer survivorship, 2024-08, Vol.18 (4), p.1370-1383

2024

Volltextzugriff (PDF)

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance

The Journal of law, medicine & ethics, 2018-03, Vol.46 (1), p.79-86

2018

Volltextzugriff (PDF)

Exploring Understanding of "Understanding": The Paradigm Case of Biobank Consent Comprehension

American journal of bioethics, 2019-05, Vol.19 (5), p.6-18

2019

Volltextzugriff (PDF)

Genotype-Driven Recruitment and the Disclosure of Individual Research Results

American journal of bioethics, 2017-04, Vol.17 (4), p.64-65

Beskow, Laura M.

2017

Volltextzugriff (PDF)

Certificates of confidentiality: privileging research data

Journal of law and the biosciences, 2024-01, Vol.11 (1), p.lsae003-lsae003

2024

Volltextzugriff (PDF)

Consent for Acute Care Research and the Regulatory "Gray Zone"

American journal of bioethics, 2020-05, Vol.20 (5), p.26-28

2020

Volltextzugriff (PDF)

Thought Leader Perspectives on Participant Protections in Precision Medicine Research

The Journal of law, medicine & ethics, 2019-03, Vol.47 (1), p.134-148

2019

Volltextzugriff (PDF)

Ethical Considerations in the Conduct of Unregulated mHealth Research: Expert Perspectives

The Journal of law, medicine & ethics, 2020-03, Vol.48 (1_suppl), p.9-36

2020

Volltextzugriff (PDF)

Protecting Participants in Genomic Research: Understanding the “Web of Protections” Afforded by Federal and State Law

The Journal of law, medicine & ethics, 2020-03, Vol.48 (1), p.126-141

2020

Volltextzugriff (PDF)

Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations

The Journal of law, medicine & ethics, 2020-03, Vol.48 (1_suppl), p.196-226

2020

Volltextzugriff (PDF)

Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.502-513

2015

Volltextzugriff (PDF)

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.440-463

2015

Volltextzugriff (PDF)

Certificates of Confidentiality: Legal Counsels' Experiences with and Perspectives on Legal Demands for Research Data

Journal of empirical research on human research ethics, 2012-10, Vol.7 (4), p.1-9

2012

Volltextzugriff (PDF)

Expert Perspectives on Oversight for Unregulated mHealth Research: Empirical Data and Commentary

The Journal of law, medicine & ethics, 2020-03, Vol.48 (1_suppl), p.138-146

2020

Volltextzugriff (PDF)

Addressing choice of law challenges in multi-state precision medicine research: experts’ assessment of key factors

Journal of law and the biosciences, 2022-01, Vol.9 (1), p.lsac013-lsac013

2022

Volltextzugriff (PDF)

Legal and Ethical Challenges of International Direct-to-Participant Genomic Research: Conclusions and Recommendations

The Journal of law, medicine & ethics, 2019-12, Vol.47 (4), p.705-731

2019

Volltextzugriff (PDF)

Certificates of Confidentiality: Protecting Human Subject Research Data in Law and Practice

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.594-609

2015

Volltextzugriff (PDF)

Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and Their Families

The Journal of law, medicine & ethics, 2015-09, Vol.43 (3), p.514-522

2015

Volltextzugriff (PDF)

Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants

The Journal of law, medicine & ethics, 2018-03, Vol.46 (1), p.87-109

2018

Volltextzugriff (PDF)

Parent Perspectives on Pediatric Genetic Research and Implications for Genotype-driven Research Recruitment

Journal of empirical research on human research ethics, 2011-12, Vol.6 (4), p.41-52

2011

Volltextzugriff (PDF)

Prospective Biorepository Participants' Perspectives on Access to Research Results

Journal of empirical research on human research ethics, 2009-09, Vol.4 (3), p.99-111

2009

Volltextzugriff (PDF)

Considering the Nature of Individual Research Results

American journal of bioethics, 2006-12, Vol.6 (6), p.38-40

Beskow, Laura M.

2006

Volltextzugriff (PDF)

Epilepsy Patient-Participants and Genetic Research Results as “Answers”

Journal of empirical research on human research ethics, 2011-12, Vol.6 (4), p.21-29

2011

Volltextzugriff (PDF)

1 – 25 von 27

Suche als RSS-Feed

Aktive Filter

ThemaSocial Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(25)
Mit Volltextzugriff
(23)

Publikationsform

Artikel
(27)

Sprache

Englisch
(27)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

3 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Direct-to-consumer genetic testing: Prospective users' attitudes toward information about ancestry and biological relationships

Thought leader perspectives on benefits and harms in precision medicine research

The lived experience of prostate cancer: 10-year survivor perspectives following contemporary treatment of localized prostate cancer

Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance

Exploring Understanding of "Understanding": The Paradigm Case of Biobank Consent Comprehension

Genotype-Driven Recruitment and the Disclosure of Individual Research Results

Certificates of confidentiality: privileging research data

Consent for Acute Care Research and the Regulatory "Gray Zone"

Thought Leader Perspectives on Participant Protections in Precision Medicine Research

Ethical Considerations in the Conduct of Unregulated mHealth Research: Expert Perspectives

Protecting Participants in Genomic Research: Understanding the “Web of Protections” Afforded by Federal and State Law

Unregulated Health Research Using Mobile Devices: Ethical Considerations and Policy Recommendations

Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations

Certificates of Confidentiality: Legal Counsels' Experiences with and Perspectives on Legal Demands for Research Data

Expert Perspectives on Oversight for Unregulated mHealth Research: Empirical Data and Commentary

Addressing choice of law challenges in multi-state precision medicine research: experts’ assessment of key factors

Legal and Ethical Challenges of International Direct-to-Participant Genomic Research: Conclusions and Recommendations

Certificates of Confidentiality: Protecting Human Subject Research Data in Law and Practice

Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and Their Families

Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research Participants

Parent Perspectives on Pediatric Genetic Research and Implications for Genotype-driven Research Recruitment

Prospective Biorepository Participants' Perspectives on Access to Research Results

Considering the Nature of Individual Research Results

Epilepsy Patient-Participants and Genetic Research Results as “Answers”

Aktive Filter

Suchergebnisse filtern