Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape

Por Holtkamp, Kim C.A., Vos, Evelien M., Rigter, Tessel, Lakeman, Phillis, Henneman, Lidewij, Cornel, Martina C.
Publicado no BMC Health Serv Res (2017)

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

Por Martens, Forike K., Huntjens, Daan W., Rigter, Tessel, Bartels, Meike, Bet, Pierre M., Cornel, Martina C.
Publicado no Front Pharmacol (2020)

Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases

Por Rigter, Tessel, Henneman, Lidewij, Broerse, Jacqueline E. W., Shepherd, Maggie, Blanco, Ignacio, Kristoffersson, Ulf, Cornel, Martina C.
Publicado em 2014

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

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

Por Rigter, Tessel, Jansen, Marleen E., de Groot, Jordy M., Janssen, Susan W.J., Rodenburg, Wendy, Cornel, Martina C.
Publicado no Front Genet (2020)

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

Por Cornel, Martina C, Rigter, Tessel, Weinreich, Stephanie S, Burgard, Peter, Hoffmann, Georg F, Lindner, Martin, Gerard Loeber, J, Rupp, Kathrin, Taruscio, Domenica, Vittozzi, Luciano
Publicado em 2014

A decade of molecular genetic testing for MODY: a retrospective study of utilization in The Netherlands

Por Weinreich, Stephanie S, Bosma, Astrid, Henneman, Lidewij, Rigter, Tessel, Spruijt, Carla MJ, Grimbergen, Anneliese JEMA, Breuning, Martijn H, de Koning, Eelco JP, Losekoot, Monique, Cornel, Martina C
Publicado no Eur J Hum Genet (2015)

Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics

Por Rigter, Tessel, Henneman, Lidewij, Kristoffersson, Ulf, Hall, Alison, Yntema, Helger G, Borry, Pascal, Tönnies, Holger, Waisfisz, Quinten, Elting, Mariet W, Dondorp, Wybo J, Cornel, Martina C
Publicado no Hum Mutat (2013)

Public support for neonatal screening for Pompe disease, a broad-phenotype condition

Por Weinreich, Stephanie Shifra, Rigter, Tessel, van El, Carla Geertruida, Dondorp, Wybo Jan, Kostense, Pieter Johannes, van der Ploeg, Ans T, Reuser, Arnold JJ, Cornel, Martina Cornelia, Hagemans, Marloes Louise Catharina
Publicado em 2012

Challenges and opportunities for ELSI early career researchers

Por Bell, Jessica, Ancillotti, Mirko, Coathup, Victoria, Coy, Sarah, Rigter, Tessel, Tatum, Travis, Grewal, Jasjote, Akcesme, Faruk Berat, Brkić, Jovana, Causevic-Ramosevac, Anida, Milovanovic, Goran, Nobile, Marianna, Pavlidis, Cristiana, Finlay, Teresa, Kaye, Jane
Publicado no BMC Med Ethics (2016)