UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 247

Sortiert nach

Evidence-Based Genetic Education of Non-Genetic-Expert Physicians: Experiences Over Three Decades in Amsterdam

Frontiers in genetics, 2019-08, Vol.10, p.712-712

Cornel, Martina C

2019

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Systematic scoping review of the concept of 'genetic identity' and its relevance for germline modification

PloS one, 2020-01, Vol.15 (1), p.e0228263-e0228263

2020

Volltextzugriff (PDF)

Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders

PloS one, 2022-06, Vol.17 (6), p.e0269719-e0269719

2022

Volltextzugriff (PDF)

Genomic newborn screening: public health policy considerations and recommendations

BMC medical genomics, 2017-02, Vol.10 (1), p.9-9, Article 9

2017

Volltextzugriff (PDF)

Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions

BMC health services research, 2017-09, Vol.17 (1), p.670-670, Article 670

2017

Volltextzugriff (PDF)

Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide

Journal of community genetics, 2021-04, Vol.12 (2), p.257-265

2021

Volltextzugriff (PDF)

Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010

European journal of human genetics : EJHG, 2013-08, Vol.21 (8), p.793-799

2013

Volltextzugriff (PDF)

Implementation of Pharmacogenetics in Primary Care: A Multi-Stakeholder Perspective

Frontiers in genetics, 2020-01, Vol.11, p.10-10

2020

Volltextzugriff (PDF)

DPD Testing Before Treatment With Fluoropyrimidines in the Amsterdam UMCs: An Evaluation of Current Pharmacogenetic Practice

Frontiers in pharmacology, 2020-01, Vol.10, p.1609-1609

2020

Volltextzugriff (PDF)

Pursuing Public Health Benefit Within National Genomic Initiatives: Learning From Different Policies

Frontiers in genetics, 2022-05, Vol.13, p.865799-865799

2022

Volltextzugriff (PDF)

Genetic Screening-Emerging Issues

Genes, 2024-05, Vol.15 (5), p.581

2024

Volltextzugriff (PDF)

Does non‐invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population‐based register study

Prenatal diagnosis, 2021-09, Vol.41 (10), p.1351-1359

2021

Volltextzugriff (PDF)

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document

European journal of human genetics : EJHG, 2014-01, Vol.22 (1), p.12-17

2014

Volltextzugriff (PDF)

Effect of comprehensive oncogenetics training interventions for general practitioners, evaluated at multiple performance levels

PloS one, 2015-04, Vol.10 (4), p.e0122648-e0122648

2015

Volltextzugriff (PDF)

Information Provision Regarding Health-Related Direct-to-Consumer Genetic Testing for Dutch Consumers: An in-Depth Content Analysis of Sellers' Websites

Genes, 2024-04, Vol.15 (4), p.517

2024

Volltextzugriff (PDF)

Personalised Health Care: Fostering Precision Medicine Advancements for Gaining Population Health Impact

1st Edition 2021, 2020

Volltextzugriff (PDF)

Predictive Value of SLCO1B1 c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users

Genes, 2023-02, Vol.14 (2), p.456

2023

Volltextzugriff (PDF)

The challenges of the expanded availability of genomic information: an agenda-setting paper

Journal of community genetics, 2018-04, Vol.9 (2), p.103-116

2018

Volltextzugriff (PDF)

How to Integrate Personalized Medicine into Prevention? Recommendations from the Personalized Prevention of Chronic Diseases (PRECeDI) Consortium

Public health genomics, 2019, Vol.22 (5/6), p.208-214

2019

Volltextzugriff (PDF)

Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder Perspective

Frontiers in pediatrics, 2021-10, Vol.9, p.706394-706394

2021

Volltextzugriff (PDF)

Expanded Neonatal Bloodspot Screening Programmes: An Evaluation Framework to Discuss New Conditions With Stakeholders

Frontiers in pediatrics, 2021-02, Vol.9, p.635353-635353

2021

Volltextzugriff (PDF)

Correction: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages

Genetics in medicine, 2019-07, Vol.21 (7), p.1669-1669

2019

Volltextzugriff (PDF)

Ephedrine treatment for autoimmune myasthenia gravis

Neuromuscular disorders : NMD, 2017-03, Vol.27 (3), p.259-265

2017

Volltextzugriff (PDF)

1 – 25 von 247

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(216)
Mit Volltextzugriff
(221)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Evidence-Based Genetic Education of Non-Genetic-Expert Physicians: Experiences Over Three Decades in Amsterdam

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

Systematic scoping review of the concept of 'genetic identity' and its relevance for germline modification

Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders

Genomic newborn screening: public health policy considerations and recommendations

Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions

Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide

Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010

Implementation of Pharmacogenetics in Primary Care: A Multi-Stakeholder Perspective

DPD Testing Before Treatment With Fluoropyrimidines in the Amsterdam UMCs: An Evaluation of Current Pharmacogenetic Practice

Pursuing Public Health Benefit Within National Genomic Initiatives: Learning From Different Policies

Genetic Screening-Emerging Issues

2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families

Does non‐invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population‐based register study

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document

Effect of comprehensive oncogenetics training interventions for general practitioners, evaluated at multiple performance levels

Information Provision Regarding Health-Related Direct-to-Consumer Genetic Testing for Dutch Consumers: An in-Depth Content Analysis of Sellers' Websites

Personalised Health Care: Fostering Precision Medicine Advancements for Gaining Population Health Impact

Predictive Value of SLCO1B1 c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users

The challenges of the expanded availability of genomic information: an agenda-setting paper

How to Integrate Personalized Medicine into Prevention? Recommendations from the Personalized Prevention of Chronic Diseases (PRECeDI) Consortium

Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder Perspective

Expanded Neonatal Bloodspot Screening Programmes: An Evaluation Framework to Discuss New Conditions With Stakeholders

Correction: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages

Ephedrine treatment for autoimmune myasthenia gravis

Suchergebnisse filtern