Found: 19
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Towards a Responsible Transition to Learning Healthcare Systems in Precision Medicine: Ethical Points to Consider.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 6, p. 539, doi. 10.3390/jpm11060539
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- Article
Public support for neonatal screening for Pompe disease, a broad-phenotype condition.
- Published in:
- 2012
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- Publication type:
- journal article
Current and Best Practices of Genetic Testing for Maturity Onset Diabetes of the Young: Views of Professional Experts.
- Published in:
- Public Health Genomics, 2015, v. 18, n. 1, p. 52, doi. 10.1159/000367963
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- Article
Challenges and opportunities for ELSI early career researchers.
- Published in:
- 2016
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- Publication type:
- journal article
Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape.
- Published in:
- 2017
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- Publication type:
- journal article
DPD Testing Before Treatment With Fluoropyrimidines in the Amsterdam UMCs: An Evaluation of Current Pharmacogenetic Practice.
- Published in:
- Frontiers in Pharmacology, 2020, p. 1, doi. 10.3389/fphar.2019.01609
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- Publication type:
- Article
A decade of molecular genetic testing for MODY: a retrospective study of utilization in The Netherlands.
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- European Journal of Human Genetics, 2015, v. 23, n. 1, p. 29, doi. 10.1038/ejhg.2014.59
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- Publication type:
- Article
A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document.
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- European Journal of Human Genetics, 2014, v. 22, n. 1, p. 12, doi. 10.1038/ejhg.2013.90
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- Publication type:
- Article
Implementation of Pharmacogenetics in Primary Care: A Multi-Stakeholder Perspective.
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- Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2020.00010
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- Publication type:
- Article
Newborn screening for pompe disease? a qualitative study exploring professional views.
- Published in:
- BMC Pediatrics, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2431-14-203
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- Publication type:
- Article
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1 - From blood spot to screening result.
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- Journal of Inherited Metabolic Disease, 2012, v. 35, n. 4, p. 603, doi. 10.1007/s10545-012-9483-0
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- Publication type:
- Article
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2 - From screening laboratory results to treatment, follow-up and quality assurance.
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- Journal of Inherited Metabolic Disease, 2012, v. 35, n. 4, p. 613, doi. 10.1007/s10545-012-9484-z
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- Publication type:
- Article
Pursuing Public Health Benefit Within National Genomic Initiatives: Learning From Different Policies.
- Published in:
- Frontiers in Genetics, 2022, p. 1, doi. 10.3389/fgene.2022.865799
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- Publication type:
- Article
Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders.
- Published in:
- PLoS ONE, 2022, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0269719
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- Publication type:
- Article
Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics.
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- Human Mutation, 2013, v. 34, n. 10, p. 1322, doi. 10.1002/humu.22370
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- Article
Opportunistische genoomscreening: normatieve reflectie.
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- Tijdschrift voor Gezondheidszorg en Ethiek, 2021, v. 31, n. 2, p. 39
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- Article
Genetic Screening—Emerging Issues.
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- Genes, 2024, v. 15, n. 5, p. 581, doi. 10.3390/genes15050581
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- Publication type:
- Article
Information Provision Regarding Health-Related Direct-to-Consumer Genetic Testing for Dutch Consumers: An in-Depth Content Analysis of Sellers' Websites.
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- Genes, 2024, v. 15, n. 4, p. 517, doi. 10.3390/genes15040517
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- Publication type:
- Article
Predictive Value of SLCO1B1 c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users.
- Published in:
- Genes, 2023, v. 14, n. 2, p. 456, doi. 10.3390/genes14020456
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- Publication type:
- Article