Genetic testing and common disorders in a public health framework: Recommendations of the European Society of Human Genetics

Por van El, Carla G, Cornel, Martina C
Publicado em 2011

Genetic testing and common disorders in a public health framework: Recommendations of the European Society of Human Genetics

Por van El, Carla G, Cornel, Martina C
Publicado em 2011

Barriers and Facilitating Factors for Implementation of Genetic Services: A Public Health Perspective

Por Cornel, Martina C., van El, Carla G.
Publicado no Front Public Health (2017)

The challenge of implementing genetic tests with clinical utility while avoiding unsound applications

Por Cornel, Martina C., van El, Carla G., Borry, Pascal
Publicado em 2012

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

Por Cornel, Martina C., van El, Carla G., Dondorp, Wybo J.
Publicado em 2011

Stakeholder Views on Active Cascade Screening for Familial Hypercholesterolemia

Por van El, Carla G., Baccolini, Valentina, Piko, Peter, Cornel, Martina C.
Publicado no Healthcare (Basel) (2018)

Governing biological material at the intersection of care and research: the use of dried blood spots for biobanking

Por Douglas, Conor M.W., van El, Carla G., Faulkner, Alex, Cornel, Martina C.
Publicado em 2012

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

Por van Schendel, Rachèl V., van El, Carla G., Pajkrt, Eva, Henneman, Lidewij, Cornel, Martina C.
Publicado no BMC Health Serv Res (2017)

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

Por Henneman, Lidewij, Vermeulen, Eric, van El, Carla G, Claassen, Liesbeth, Timmermans, Danielle R M, Cornel, Martina C
Publicado em 2013

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

Por van El, Carla G, Rigter, Tessel, Reuser, Arnold JJ, van der Ploeg, Ans T, Weinreich, Stephanie S, Cornel, Martina C
Publicado em 2014

Value-based genomic screening: exploring genomic screening for chronic diseases using triple value principles

Por Dombrádi, Viktor, Pitini, Erica, van El, Carla G., Jani, Anant, Cornel, Martina, Villari, Paolo, Gray, Muir, Bíró, Klára
Publicado no BMC Health Serv Res (2019)

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

Por Goekoop, Floor M., van El, Carla G., Widdershoven, Guy A. M., Dzinalija, Nadza, Cornel, Martina C., Evans, Natalie
Publicado no PLoS One (2020)

Reply to Bombard and Mighton

Por Carrieri, Daniele, Howard, Heidi C., Clarke, Angus J., Stefansdottir, Vigdis, Cornel, Martina C., van El, Carla G., Forzano, Francesca
Publicado no Eur J Hum Genet (2019)

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

Por Howard, Heidi C., van El, Carla G., Forzano, Francesca, Radojkovic, Dragica, Rial-Sebbag, Emmanuelle, de Wert, Guido, Borry, Pascal, Cornel, Martina C.
Publicado no Eur J Hum Genet (2017)

ESHG PPPC Comments on postmortem use of genetic data for research purposes

Por Fellmann, Florence, Rial-Sebbag, Emmanuelle, Patch, Christine, Hentze, Sabine, Stefandottir, Vigdis, Mendes, Álvaro, van El, Carla G., Cornel, Martina C., Forzano, Francesca
Publicado no Eur J Hum Genet (2019)

Parental perspectives on retention and secondary use of neonatal dried bloodspots: a Dutch mixed methods study

Por Jansen, Marleen E., van den Bosch, Lion J. M., Hendriks, Marjolein J., Scheffer, Mariska M. J., Heijnen, Marie-Louise, Douglas, Conor M. W., van El, Carla G.
Publicado no BMC Pediatr (2019)

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

Por Jans, Suze M.P.J., van El, Carla G., Houwaart, Eddy S., Westerman, Marjan J., Janssens, Rien J.P.A., Lagro-Janssen, Antoinette L.M., Plass, Anne Marie C., Cornel, Martina C.
Publicado em 2011

Human germline gene editing: Recommendations of ESHG and ESHRE

Por de Wert, Guido, Pennings, Guido, Clarke, Angus, Eichenlaub-Ritter, Ursula, van El, Carla G., Forzano, Francesca, Goddijn, Mariëtte, Heindryckx, Björn, Howard, Heidi C., Radojkovic, Dragica, Rial-Sebbag, Emmanuelle, Tarlatzis, Basil C., Cornel, Martina C.
Publicado no Eur J Hum Genet (2018)

Human germline gene editing. Recommendations of ESHG and ESHRE(†)(‡)

Por de Wert, Guido, Pennings, Guido, Clarke, Angus, Eichenlaub-Ritter, Ursula, van El, Carla G, Forzano, Francesca, Goddijn, Mariëtte, Heindryckx, Björn, Howard, Heidi C, Radojkovic, Dragica, Rial-Sebbag, Emmanuelle, Tarlatzis, Basil C, Cornel, Martina C
Publicado no Hum Reprod Open (2018)

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

Por De Wert, Guido, Heindryckx, Björn, Pennings, Guido, Clarke, Angus, Eichenlaub-Ritter, Ursula, van El, Carla G., Forzano, Francesca, Goddijn, Mariëtte, Howard, Heidi C., Radojkovic, Dragica, Rial-Sebbag, Emmanuelle, Dondorp, Wybo, Tarlatzis, Basil C., Cornel, Martina C.
Publicado no Eur J Hum Genet (2018)