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A case study of haemoglobinopathy screening in the Netherlands: witnessing the past, lessons for the future

artículo científico publicado en 2011

Genetic testing and common disorders in a public health framework

artículo científico publicado en 2011

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders

artículo científico publicado en 2011

Newborn screening for pompe disease? a qualitative study exploring professional views

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

artículo científico publicado en 2020

Severely impaired health status at diagnosis of Pompe disease: a cross-sectional analysis to explore the potential utility of neonatal screening.

artículo científico publicado en 2012

The promises of genomic screening: building a governance infrastructure. Special issue: genetics and democracy

artículo científico publicado en 2011

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics

artículo científico publicado en 2013

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics

artículo científico publicado en 2013

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