Moving somatic gene editing to the clinic: routes to market access and reimbursement in Europe

por Rigter, Tessel, Klein, David, Weinreich, Stephanie S., Cornel, Martina C.
Publicado 2021

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

por Cornel, Martina C., Rigter, Tessel, Jansen, Marleen E., Henneman, Lidewij
Publicado 2020

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

por Onstwedder, Suzanne M., Jansen, Marleen E., Leonardo Alves, Teresa, Cornel, Martina C., Rigter, Tessel
Publicado 2022

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 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 2020

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 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 2020

Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders

por van Dijke, Ivy, van El, Carla G., Lakeman, Phillis, Goddijn, Mariëtte, Rigter, Tessel, Cornel, Martina C., Henneman, Lidewij
Publicado 2022

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 2014

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 2013

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

por Jansen, Marleen E., Rigter, Tessel, Fleur, Thom M. C., Souverein, Patrick C., Verschuren, W. M. Monique, Vijverberg, Susanne J., Swen, Jesse J., Rodenburg, Wendy, Cornel, Martina C.
Publicado 2023

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 2012

Towards a Responsible Transition to Learning Healthcare Systems in Precision Medicine: Ethical Points to Consider

por Wouters, Roel H. P., van der Graaf, Rieke, Rigter, Tessel, Bunnik, Eline M., Ploem, M. Corrette, de Wert, Guido M. W. R., Dondorp, Wybo J., Cornel, Martina C., Bredenoord, Annelien L.
Publicado 2021

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 2016