UB Paderborn / Katalog / Suche / in CDI

Willingness to donate genomic and other medical data: results from Germany

European journal of human genetics : EJHG, 2020-08, Vol.28 (8), p.1000-1009

2020

Link zum Volltext

Verfügbarkeit prüfen

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

European journal of human genetics : EJHG, 2015-03, Vol.23 (11), p.1438-1450

2015

Link zum Volltext

Verfügbarkeit prüfen

Attitudes of publics who are unwilling to donate DNA data for research

European journal of medical genetics, 2019-05, Vol.62 (5), p.316-323

2019

Link zum Volltext

Verfügbarkeit prüfen

Transparency, consent and trust in the use of customers' data by an online genetic testing company: an Exploratory survey among 23andMe users

New genetics and society, 2020-10, Vol.39 (4), p.459-482

2020

Link zum Volltext

Verfügbarkeit prüfen

Attitudes and experiences of European clinical geneticists towards direct-to-consumer genetic testing: a qualitative interview study

New genetics and society, 2019-10, Vol.38 (4), p.410-429

2019

Link zum Volltext

Verfügbarkeit prüfen

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

Personalized medicine, 2018-07, Vol.15 (4), p.311-318

2018

Link zum Volltext

Verfügbarkeit prüfen

A review of the barriers to sharing in biobanking

Biopreservation and biobanking, 2013-12, Vol.11 (6), p.339

2013

Link zum Volltext

Verfügbarkeit prüfen

Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?

American journal of human genetics, 2020-10, Vol.107 (4), p.743-752

2020

Link zum Volltext

Verfügbarkeit prüfen

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

European journal of human genetics : EJHG, 2015-11, Vol.23 (11), p.1438-1450

2015

Link zum Volltext

Verfügbarkeit prüfen

Whole-genome sequencing in health care

European journal of human genetics : EJHG, 2013-06, Vol.21 (S1), p.S1

2013

Link zum Volltext

Verfügbarkeit prüfen

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

European journal of human genetics : EJHG, 2019-12, Vol.27 (12), p.1763-1773

2019

Link zum Volltext

Verfügbarkeit prüfen

Responsible implementation of expanded carrier screening

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.e1-e12

2016

Link zum Volltext

Verfügbarkeit prüfen

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.169-182

2019

Link zum Volltext

Verfügbarkeit prüfen

One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans

European journal of human genetics : EJHG, 2018-01, Vol.26 (1), p.1-11

2018

Link zum Volltext

Verfügbarkeit prüfen

Moving towards a cure in genetics: what is needed to bring somatic gene therapy to the clinic?

European journal of human genetics : EJHG, 2019-03, Vol.27 (3), p.484-487

2019

Link zum Volltext

Verfügbarkeit prüfen

Anxiety delivered direct-to-consumer: are we asking the right questions about the impacts of DTC genetic testing?

Journal of medical genetics, 2016-12, Vol.53 (12), p.798-799

2016

Link zum Volltext

Verfügbarkeit prüfen

Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories

Journal of community genetics, 2011-09, Vol.2 (3), p.135-146

2011

Link zum Volltext

Verfügbarkeit prüfen

Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries

Genome medicine, 2021-05, Vol.13 (1), p.92-92, Article 92

2021

Link zum Volltext

Verfügbarkeit prüfen

‘It’s much more grey than black and white’: clinical geneticists’ views on the oversight of consumer genomics in Europe

Personalized medicine, 2020-03, Vol.17 (2), p.129-140

2020

Link zum Volltext

Verfügbarkeit prüfen

Human germline gene editing: Recommendations of ESHG and ESHRE

European journal of human genetics : EJHG, 2018-04, Vol.26 (4), p.445-449

2018

Link zum Volltext

Verfügbarkeit prüfen

Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE

European journal of human genetics : EJHG, 2018-04, Vol.26 (4), p.450-470

2018

Link zum Volltext

Verfügbarkeit prüfen

Genetic testing: anonymity of sperm donors under threat

Nature (London), 2013-04, Vol.496 (7444), p.169-169

2013

Link zum Volltext

Verfügbarkeit prüfen

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

Human reproduction (Oxford), 2011-05, Vol.26 (5), p.972-977

2011

Link zum Volltext

Verfügbarkeit prüfen

Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market

Journal of community genetics, 2010-09, Vol.1 (3), p.101-106

2010

Link zum Volltext

Verfügbarkeit prüfen

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

European journal of human genetics : EJHG, 2015-04

2015

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

Willingness to donate genomic and other medical data: results from Germany

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Attitudes of publics who are unwilling to donate DNA data for research

Transparency, consent and trust in the use of customers' data by an online genetic testing company: an Exploratory survey among 23andMe users

Attitudes and experiences of European clinical geneticists towards direct-to-consumer genetic testing: a qualitative interview study

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

A review of the barriers to sharing in biobanking

Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Whole-genome sequencing in health care

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

Responsible implementation of expanded carrier screening

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans

Moving towards a cure in genetics: what is needed to bring somatic gene therapy to the clinic?

Anxiety delivered direct-to-consumer: are we asking the right questions about the impacts of DTC genetic testing?

Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories

Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries

‘It’s much more grey than black and white’: clinical geneticists’ views on the oversight of consumer genomics in Europe

Human germline gene editing: Recommendations of ESHG and ESHRE

Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE

Genetic testing: anonymity of sperm donors under threat

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

Suchergebnisse filtern